Recalls in Puerto Rico (page 9)
3814 recalls.
- Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Citrasate recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Complaints of blue-green discoloration in product - NaturaLyte recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Complaints of blue-green discoloration in product - GRANUFLO Dry Acid Concentrate: Product Numbers: 0FD2251-3B recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Complaints of blue-green discoloration in product - Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog... recall (B Braun Medical Inc)
Medical deviceClass IIReported September 9, 2026 · Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label. - Velys Enabling Tech Robotic-Assist Station REF: 451611001 recall (Medos International Sarl)
Medical deviceClass IIReported September 9, 2026 · Software issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation or instrument positioning. - 5008X HD/HDF with Twister Blood Tubing Set Part Number 03-5350-8 recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to... - 5008X HD/HDF with CLiC Blood Tubing Set Part number 03-5300-3C recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to... - 5008X HD/HDF Standard Blood Tubing Set Part Number 03-5300-3 recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to... - 5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6 recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to... - LUX-Dx recall (Boston Scientific Corporation)
Medical deviceClass IIReported September 9, 2026 · There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed... - LUX-Dx recall (Boston Scientific Corporation)
Medical deviceClass IIReported September 9, 2026 · There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed... - LUX-Dx recall (Boston Scientific Corporation)
Medical deviceClass IIReported September 9, 2026 · There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ORTHO... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators CATARACT... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators C-SECTION... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators LABOR... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PATIENT... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators DELUXE... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ADULT... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators IV START... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BASIN... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators OPEN... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PAIN PRE... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Baxter Novum IQ Syringe Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 9, 2026 · A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused... - Baxter Novum IQ Syringe Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 9, 2026 · A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused... - HEALON EndoCoat PRO recall (Johnson & Johnson Surgical Vision, Inc.)
Medical deviceClass IIReported September 9, 2026 · Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is encountered... - Medline Convenience Kits: 1) BLOOD DRAW KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) ORTHO ASPIRATION KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) EYE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) C-SECTION PREP recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) LABOR CDS recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) PRE-OP KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) BLOOD CULTURE TRAY PEDIATRIC recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) IV START KIT LAB DRAW-SH recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) ARTERIAL LINE INSERTION KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) IV START KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) ULTRASOUND BREAST PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) COLORECTAL ME recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) IVS BLOOD CULTURE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) DYKM1414 recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) CDS840396X recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) DRAWER 9 CRICOTHYROTOMY KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Halyard medical convenience kits labeled as: 1) A-P PACK - 205936 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 9, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - 1) NEURO recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 9, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - Halyard medical convenience kits labeled as: 1) ENT recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 9, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - MONDRAKER USA Recalls Mountain Bicycles Equipped with ONOFF S9 Carbon MTB Handlebars Due to Risk of Serious Injury or Death from Fall Hazard
Consumer productReported September 3, 2026 · The affected handlebars may crack or fracture during use, which can lead to loss of control, posing a risk of serious injury or death from fall hazard. - Clorox Puerto Rico Recalls 6 Million Scented Mistolin and Lestoil Multi-Purpose Cleaners Due to Risk of Exposure to Bacteria
Consumer productReported September 3, 2026 · The recalled products may contain bacteria, including Pseudomonas aeruginosa, which is an environmental organism found widely in soil and water. People with... - Truststone Group Recalls XO Poppy Power Trip Magnetic Wireless Power Banks Due to Fire and Burn Hazards; Sold Exclusively at TJX and Marshalls Stores
Consumer productReported September 3, 2026 · The lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers. - Skip Hop Recalls Baby Sesame Street Elmo Silicone Teethers Due to Risk of Serious Injury or Death from Choking Hazard
Consumer productReported September 3, 2026 · The black eyes can detach from the recalled teether if frozen, posing a risk of serious injury or death from a choking hazard. - GIHNJSI Squeezy Dumplings Toys Recalled Due to Serious Ingestion, Choking and Obstruction Hazards; Sold on Amazon by Chenyuanhui
Consumer productReported September 3, 2026 · The squeezy toys contain water beads. If ingested, water beads expand and can pose deadly ingestion, choking, and intestinal obstruction hazards inside a... - OKK Trading Recalls Rainbow Mystery Squishy Bun Toys Due to Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys
Consumer productReported September 3, 2026 · The squishy bun toys violate the mandatory safety standard for toys because the water beads inside the dumplings expand larger than permitted, posing a deadly... - Gizoon Direct Recalls Six-Drawer Double Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units
Consumer productReported September 3, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - Branch Recalls Ergonomic Chairs Due to Fall Hazard
Consumer productReported September 3, 2026 · The backrests of the chairs can detach, posing a fall hazard to consumers. - Daikin Comfort Technologies Manufacturing Recalls Amana Through-The-Wall Air Conditioners and Heat Pumps Due to Risk of Serious Injury from Fire
Consumer productReported September 3, 2026 · The snubber circuit can emit flames if it shorts, posing a risk of serious injury due to fire hazard. - Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Loyoda Direct and Loyoda
Consumer productReported September 3, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed... - SHEIN Distribution Corporation Recalls Spiral Toys Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Ball Ban
Consumer productReported September 3, 2026 · The toys violate the small ball ban because they contain small balls and are intended for children under three years of age, posing a deadly choking hazard. - Audio Partnership Recalls Cambridge Audio Yoyo (M) Portable Bluetooth Speakers Due to Fire Hazard
Consumer productReported September 3, 2026 · The lithium-ion batteries in the Cambridge Audio Yoyo (M) Portable Bluetooth Speaker can overheat, posing a fire hazard. - Nanjing Wu Hai Smart Home Appliance Store Recalls Alanca 6-Drawer Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units
Consumer productReported September 3, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts recall (Byron White Formulas, Inc.)
FoodClass IIReported September 2, 2026 · Label does not declare walnuts in English - Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts recall (Byron White Formulas, Inc.)
FoodClass IIReported September 2, 2026 · Label does not declare walnuts in English - Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts recall (Byron White Formulas, Inc.)
FoodClass IIReported September 2, 2026 · Label does not declare walnuts in English - Outshine Fruit Bars Strawberry recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bars Black Cherry recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bars Tangerine recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bars Grape recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bar Watermelon recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bars Strawberry recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Horizon Organic ORG ASEP CHOC MILK 1% 8OZ 12 CT recall (Horizon Organic Dairy, LLC)
FoodClass IIReported September 2, 2026 · Product has the potential to be spoiled. - Lactated Ringer's Injection USP recall (B BRAUN MEDICAL INC)
DrugClass IReported September 2, 2026 · Presence of Particulate matter. - Ramipril Capsules USP recall (Hikma Pharmaceuticals USA INC.)
DrugClass IIReported September 2, 2026 · Failed Impurities/Degradation Specifications: OOS result obtained for a process impurity, dicyclohexylurea (DCU). - Tyenne recall (Fresenius Kabi USA, LLC)
DrugClass IReported September 2, 2026 · Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles. - Paxil CR recall (Apotex Corp.)
DrugClass IIReported September 2, 2026 · Failed Dissolution Specifications; product failed to meet 24-month stability testing acceptance criteria - Acthar Gel recall (Mallinckrodt Hospital Products Inc.)
DrugClass IIReported September 2, 2026 · Presence of particulate matter: glass and stopper piece - Zicam recall (Church & Dwight Co., Inc.)
DrugClass IIReported September 2, 2026 · CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing - Clobetasol Propionate Cream USP recall (Lupin Pharmaceuticals Inc.)
DrugClass IIReported September 2, 2026 · Failed content uniformity specifications. - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - POWERSEAL 5 MM recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported September 2, 2026 · Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device. - ORT300 recall (IMRIS Imaging Inc)
Medical deviceClass IIReported September 2, 2026 · The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and... - ORT200 recall (IMRIS Imaging Inc)
Medical deviceClass IIReported September 2, 2026 · The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and... - healthmark ProChek-W Protein Test for Robotic Arms recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported September 2, 2026 · Test manufactured with an expired ingredient which may present as either a false negative or positive. - healthmark ProChek-II recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported September 2, 2026 · Test manufactured with an expired ingredient which may present as either a false negative or positive. - FUJIFILM Synapse PACS software v7.4.310 recall (FUJIFILM Healthcare Americas Corporation)
Medical deviceClass IIReported September 2, 2026 · Software issue may cause the ruler measurement to be inaccurate. - Medline convenience kits labeled as: 1) LAMI FUSION recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) CMH LITHO MINOR PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer