Recalls in Louisiana (page 33)
3956 recalls.
- Med Nap BZK Antiseptic Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Medi-First Antiseptic Wipes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Savannah Antibacterial Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Max Packaging Antibacterial Towelette recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - 1) BZK Antiseptic Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - First Aid Only BZK Antiseptic Towelette recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Dukal BZK Antiseptic Towelette recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - First Aid Only BZK Antiseptic Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - First Aid Only BZK Antiseptic Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Metoprolol Succinate Extended-Release Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported March 11, 2026 · Failed Dissolution Specifications - Metoprolol Succinate Extended-Release Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported March 11, 2026 · Failed Dissolution Specifications - Metoprolol Succinate Extended-Release Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported March 11, 2026 · Failed Dissolution Specifications - Metoprolol Succinate Extended-Release Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported March 11, 2026 · Failed Dissolution Specifications - Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S ... recall (Diagnostica Stago, Inc.)
Medical deviceClass IIReported March 11, 2026 · The potential of out-of-range results and an underestimation of the free protein S level in normal patient plasmas. The defect only affects normal-range values. - Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. ... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Potential for rubber fragment detachment during use. - Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. ... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Potential for rubber fragment detachment during use. - CS300 IABP. Software Version CS300 IABP C.01. recall (Datascope Corp.)
Medical deviceClass IIReported March 11, 2026 · The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated. - CS100 IABP. Software Version CS100 IABP Q.01. recall (Datascope Corp.)
Medical deviceClass IIReported March 11, 2026 · The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated. - Atellica CH Urine Albumin recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported March 11, 2026 · Falsely depressed UAlb patient results may occur. Affected samples with any urine albumin concentration above the UAlb measuring interval >40.0 mg/dL may... - Brand Name: B. Braun Product Name: 21GA WINGED INF SET Model/Catalog Number: 7M2802 ... recall (B Braun Medical Inc)
Medical deviceClass IIReported March 11, 2026 · The potential for the needle tip to be dull/blunt, difficult to advance, and/or break. - Brand Name: B. Braun Product Name: 21GA WINGED INFUSION recall (B Braun Medical Inc)
Medical deviceClass IIReported March 11, 2026 · The potential for the needle tip to be dull/blunt, difficult to advance, and/or break. - Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Winged INF ... recall (B Braun Medical Inc)
Medical deviceClass IIReported March 11, 2026 · The potential for the needle tip to be dull/blunt, difficult to advance, and/or break. - Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE Lithotripsy... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the... - Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-SE... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the... - Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse-SE... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the... - cobas pro integrated solutions with cobas c 503 analytical units: cobas pro sample... recall (Roche Diagnostics Operations, Inc.)
Medical deviceClass IIReported March 11, 2026 · Software defect, which allows the system to accept erroneous, non-monotonous calibrations for Spline-type assays. Cobas pro integrated solutions is an... - GE Healthcare Centricity Universal Viewer Zero Footprint Client recall (GE Healthcare)
Medical deviceClass IIReported March 11, 2026 · Under certain workflows, patient information shown in the viewer may not match the images displayed on Centricity Universal Viewer Zero Footprint Client (ZFP)... - Impella RP. Product Code: 0046-0011. recall (Abiomed, Inc.)
Medical deviceClass IReported March 11, 2026 · Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift. - Impella RP Flex with SmartAssist. Product Code: 1000323. recall (Abiomed, Inc.)
Medical deviceClass IReported March 11, 2026 · Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift. - Impella RP with SmartAssist. Product Code: 0046-0035. recall (Abiomed, Inc.)
Medical deviceClass IReported March 11, 2026 · Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift. - Cubimana Island Storm 3 In 1 Building Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by RBS Toys
Consumer productReported March 5, 2026 · The Island Storm Building Sets violate the mandatory safety standard for toys because the battery compartment within the LED light piece contains button cell... - HALO Dream Recalls Magic Sleepsuits Due to Choking Hazard
Consumer productReported March 5, 2026 · The zipper head can detach from certain sleepsuits, posing a choking hazard to infants. - Tomum Minoxidil Hair Serum Spray Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Distributed by Belleka
Consumer productReported March 5, 2026 · The hair serum contains minoxidil, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The hair serum's bottles are... - Unique Brands Com Recalls Forever 21 Pajama Pants Due to Risk of Serious Injury or Death from Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear
Consumer productReported March 5, 2026 · The recalled children's pajama pants violate the mandatory standards for flammability of children's sleepwear, posing a burn hazard and risk of serious injury... - Mung Beans packaged in 4lb polybags recall (LUBNA QUALITY PRODUCTS INC.)
FoodClass IIIReported March 4, 2026 · Presence of Thiamethoxam-PESTICIDE - Brand Name: Reverse Shoulder Prosthesis recall (Encore Medical, LP)
Medical deviceClass IIReported March 4, 2026 · Knee and Humeral socket implants contain incorrect labeling. - Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS recall (Encore Medical, LP)
Medical deviceClass IIReported March 4, 2026 · Knee and Humeral socket implants contain incorrect labeling. - Brand Name: Reverse Shoulder Prosthesis recall (Encore Medical, LP)
Medical deviceClass IIReported March 4, 2026 · Knee and Humeral socket implants contain incorrect labeling. - Gerber Arrowroot Biscuits recall (Gerber Products Company dba Nestle Infant Nutrition)
FoodClass IIReported March 4, 2026 · Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft... - BioGlo Fluorescein Sodium Ophthalmic Strips USP recall (Wizcure Pharmaa Private Limited)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices. - Bio Glo Fluorescein Sodium Ophthalmic Strips USP recall (Wizcure Pharmaa Private Limited)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices. - CHNaO Fluorescein Sodium Ophthalmic Strips recall (Wizcure Pharmaa Private Limited)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices. - Vista Gonio Eye Lubricant recall (Wizcure Pharmaa Private Limited)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices. - Vista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops Advanced Dry Eye Relief... recall (Wizcure Pharmaa Private Limited)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices. - Vista Gel Hypromellose USP 0.3% w/v recall (Wizcure Pharmaa Private Limited)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices. - Vista Tears Polyethylene Glycol 400 0.4% w/v recall (Wizcure Pharmaa Private Limited)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices. - Eptifibatide Injection recall (Slate Run Pharmaceuticals)
DrugClass IIIReported March 4, 2026 · Labeling: Not Elsewhere Classified. The carton for Eptifibatide Injection 75 mg/100 mL states 75 mg/100 mL vial for weight-adjusted bolus dosing. The approved... - Amantadine HCl recall (AvKARE)
DrugClass IIReported March 4, 2026 · Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution. - Adbry recall (LEO PHARMA INC)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber. - Campy CVA Medium 100/PK recall (Remel, Inc)
Medical deviceClass IIReported March 4, 2026 · Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium. - Octopus Nuvo Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported March 4, 2026 · During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the... - Adapt Pump recall (Agiliti Health - Ellis)
Medical deviceClass IIReported March 4, 2026 · Agiliti identified an issue where the Adapt Pump (61600200-Adapt Pump) supplied with all Adapt Line support surfaces does not re-engage the Microclimate... - Convenience kits containing Tego Connectors Medline DIALYSIS DRSNG CHNG SKU DYNDC3167 recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing.... - Convenience kits containing Tego Connectors: Medline DIALYSIS DRESSING CHANGE SKU... recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing.... - Medline kits containing Tego Connectors Medline APHERESIS SUBQPORT ACCESS KIT SKU... recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing.... - Convenience kits used for dialysis maintenance Medline ADD A CATH DIALYSIS KIT SKU... recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing.... - Medline Kits containing Tego Connectors Medline DIALYSIS ON/OFF KIT SKU EBSI1746 recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing.... - Medline Kits containing Tego Connectors: Medline IR Pack recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing.... - PIE PAK Models: P2HC-A recall (Edermy LLC)
Medical deviceClass IIReported March 4, 2026 · Lack of 510K clearance - PIE Trolley System Model: 2005 recall (Edermy LLC)
Medical deviceClass IIReported March 4, 2026 · Lack of 510K clearance - Meijer STERILE saline wound wash recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility... - Medline Convenience Kits: 1) NAIL KIT recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility... - Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility... - Medline Convenience Kits: 1) NAIL KIT recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility... - Medline Sterile Saline Wound Wash recall (Medline Industries, LP)
Medical deviceClass IIReported March 4, 2026 · Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility... - Evajoy Above-Ground Pools 48 Inches and Taller Recalled Due to Drowning Hazard; Manufactured by Shenzhen Danya Tech
Consumer productReported February 27, 2026 · The compression strap that surrounds the outside of the pool legs may create a foothold, allowing a child access to the pool, posing a drowning risk. - Babysense Max View Baby Monitors Recalled Due to Fire Hazard; Manufactured by Hisense
Consumer productReported February 27, 2026 · The display or "parent" unit of the Max View baby monitors can overheat and/or spark when charging, posing a fire hazard to consumers. - Andersen Windows Recalls Window Opening Control Devices Sold as Kits or Installed on 100 Series Casement Windows Due to Fall and Serious Injury Hazards
Consumer productReported February 27, 2026 · The window opening control devices can break or detach after accidental or other impact, allowing the window to be opened, posing fall and serious injury... - SumDirect LED Mini Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
Consumer productReported February 27, 2026 · The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain button cell... - Todson Recalls Concord Bicycle Helmets Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets
Consumer productReported February 27, 2026 · The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the retention system and positional... - Joyreal Busy Board Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking and Laceration Hazards; Violate Small Parts Ban and Mandatory Standard for Toys; Sold on Amazon by Indream Store
Consumer productReported February 27, 2026 · The recalled children's toys violate the small parts ban because the small mirror can detach from the toy, posing a deadly choking hazard. In addition, the... - Zelbuck Children's Chess Games Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by n b plus
Consumer productReported February 27, 2026 · The recalled children's chess games violate the mandatory standard for toys because they contain loose magnets posing an ingestion hazard to children. When... - TheKiddoSpace Recalls Children's Sensory Swing Due to Risk of Serious Injury or Death from Strangulation
Consumer productReported February 27, 2026 · The recalled swing's flexible fabric can form loops that can entangle a child's head or neck, posing a risk of serious injury or death from strangulations. - TheKiddoSpace Recalls Children's Christmas Tree Play Sets Due to Risk of Injury from Lead Exposure; Violates Federal Lead Content Ban and Mandatory Standard for Toys
Consumer productReported February 27, 2026 · The zipper pull on the music box compartment of the recalled Christmas Tree Toys contain levels of lead that exceed the federal lead content ban. Lead is toxic... - TheKiddoSpace Recalls Peg Doll Children's Toys Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Parts Ban
Consumer productReported February 27, 2026 · The recalled toys are intended for children under three years old and the toy's peg dolls can block a child's airway, which violate the small parts ban, posing... - TheKiddoSpace Recalls LED Soccer Hover Balls Due to Serious Risk of Injury from Burn Hazard; Violates Mandatory Standard for Toys
Consumer productReported February 27, 2026 · The surface temperature of the recalled toys' batteries exceeds the allowable limit, which violates the standard for toys, posing a risk of burn injuries. - TheKiddoSpace Recalls Children's Montessori Egg Puzzle Toys Due to Risk of Serious Injury or Death from Choking Hazard
Consumer productReported February 27, 2026 · The recalled toys are intended for children under three years of age and the eggs can block a child's airway, posing a risk of choking and death to children. - TheKiddoSpace Recalls Children's Flashcard Talking Toys Due to Risk of Injury from Lead and Phthalate Exposure; Violates Federal Lead Content and Phthalates Bans and Standard for Toys
Consumer productReported February 27, 2026 · The recalled children's flashcard toy sets contain levels of lead that exceed the federal lead content ban and levels of phthalates that exceed the federal... - TheKiddoSpace Recalls Reusable Water Balloons Due to Risk of Injury from Phthalate Exposure; Violate Federal Phthalates Ban
Consumer productReported February 27, 2026 · The cord lock on the recalled water ballons' storage bags contain a regulated phthalate, which violate the federal phthalate ban. Phthalates are toxic if... - TheKiddoSpace Recalls Children's Fingerpainting Kits Due to Risk of Injury from Hazardous Substances and Phthalate Exposure; Violates Federal Hazardous Substances Act and Phthalates Ban
Consumer productReported February 27, 2026 · The recalled children’s fingerpainting kits contain the hazardous substances methanol and ethylene glycol and are intended for children under 12 years of age... - TheKiddoSpace Recalls Children's Handwriting Practice Kits Due to Risk of Injury from Lead Exposure; Violates Federal Lead Content Ban
Consumer productReported February 27, 2026 · The pens in the recalled children's handwriting kits contain levels of lead in the nib that exceed the federal lead content ban. Lead is toxic if ingested by... - TheKiddoSpace Recalls Children's Story Books Due to Choking Hazard
Consumer productReported February 27, 2026 · The recalled book's felt parts can detach, posing a choking hazard. - Grtard Magnetic Stick Figure Toy Sets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys
Consumer productReported February 27, 2026 · The magnetic stick figure toy sets violate the mandatory standard for toys because they contain loose magnets, posing an ingestion hazard to children. When... - Bicystar High Chairs Recalled Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards; Violates Mandatory Standard for High Chairs
Consumer productReported February 27, 2026 · The high chairs violate the mandatory standard for high chairs because they were sold without the required attached crotch restraint, posing a deadly fall... - Magnetic Chess Games Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Kaiwenshangpin
Consumer productReported February 27, 2026 · The recalled magnetic chess games violate the mandatory standard for toys because they contain loose magnets posing an ingestion hazard to children. When... - Trankerloop Baby Bath Seats Recalled Due to Risk of Serious Injury or Death to Children from Drowning; Violates Mandatory Standard for Infant Bath Seats
Consumer productReported February 27, 2026 · The recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, posing a risk of serious... - Magnetic Chess Games Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Yiruikeji2024
Consumer productReported February 27, 2026 · The recalled magnetic chess games violate the mandatory standard for toys because they contain loose magnets posing an ingestion hazard to children. When... - Surreal Brands Recalls Children's Tubby Tots Fizzy Flask Bath Magic Bath Foam Sets Due to Impact Hazard
Consumer productReported February 27, 2026 · Moisture trapped inside the bath foam set container can cause pressure to build up, allowing pieces to be forcefully ejected when opened, posing an impact... - Somgem Pig and Yomin Toilet Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violates Mandatory Standard for Cigarette Lighters; Sold on Amazon by Elepdv
Consumer productReported February 27, 2026 · The recalled pig and toilet lighters violate the mandatory standard for cigarette lighters because they do not have the required child-resistant mechanisms... - Royal Oak Enterprises Recalls Lighters Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violates Mandatory Standard for Multipurpose Lighters
Consumer productReported February 27, 2026 · The recalled lighters violate the mandatory standard for multipurpose lighters because they do not have the required child-resistant mechanisms, posing a risk... - Dupray USA Recalls Neat Steam Cleaners Due to Risk of Burn Hazards or Serious Injury
Consumer productReported February 27, 2026 · The steam cleaner's boiler can rupture if it is overfilled, corroded and the pressure release valve malfunctions, posing risk of burn hazards or serious injury... - PQL Recalls High Bay Linear LED Light Fixtures Due to Fire Hazard
Consumer productReported February 27, 2026 · The retaining pins used to secure the LED board inside some units can degrade, the LED board to come loose inside the fixture, posing a fire hazard. - Sanven Technology Recalls Vevor Baby Gates Due to Risk of Serious Injury from Entrapment Hazard; Violates Mandatory Standard for Gates and Enclosures
Consumer productReported February 27, 2026 · The recalled gates violate the mandatory standard for expansion gates and expandable enclosures because a child's torso can fit through the opening between the... - Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset recall (Pure Solutions, Inc.)
FoodClass IIReported February 25, 2026 · Label declares bovine colostrum but does not declare milk allergen. - Da Vinci 5 ASSY recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported February 25, 2026 · An error event following the release of a software version for the surgical system that can result in loss of user interface content on an external monitor or... - MOLLI 2 System System includes: MM1000 recall (Stryker Corporation)
Medical deviceClass IIReported February 25, 2026 · Due to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target... - Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software... recall (Centinel Spine, Inc.)
Medical deviceClass IIReported February 25, 2026 · Products were mislabeled as the 6mm product but included the 5 mm product. - MONARCH Platform recall (Auris Health, Inc)
Medical deviceClass IIReported February 25, 2026 · Device for bronchoscopic visualization, patient airway access has software issue: if application restarts after patient-side selection, prior to bronchoscope... - Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth... recall (Bard Peripheral Vascular Inc)
Medical deviceClass IIReported February 25, 2026 · Due to damage to outer tray that can potentially compromise the sterile barrier - Why Not Natural Moringa Capsules 120 capsule bottle marked with lot # A25G051 on the... recall (Art Monkey LLC dba Why Not Natural)
FoodClass IReported February 25, 2026 · Potential to be contaminated with Salmonella