Recalls in March 2026
465 recalls.
- Kian Pee Wan Capsules recall (Buy-Herbal)
DrugClass IReported August 19, 2026 · Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine. - Brand Name: U2 Total Knee System Product Name: Femoral offset bushing recall (United Orthopedic Corp.)
Medical deviceClass IIReported August 12, 2026 · Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant. - Brand Name: U2 Total Knee System Product Name: Femoral offset bushing recall (United Orthopedic Corp.)
Medical deviceClass IIReported August 12, 2026 · Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant. - Nerivio Infinity. Model/Catalog Number: FGD000100. Software Version: FW Version 4.1.2.0 recall (THERANICA BIOELECTRONICS LTD)
Medical deviceClass IIReported August 12, 2026 · Potential for the batter to have a thermal-runway event during charging, resulting in smoke and odor. - Photera 600 3-D recall (Daavlin Distributing Company)
Medical deviceClass IIReported July 22, 2026 · Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000... - Photera 600 recall (Daavlin Distributing Company)
Medical deviceClass IIReported July 22, 2026 · Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000... - Photera 400 recall (Daavlin Distributing Company)
Medical deviceClass IIReported July 22, 2026 · Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000... - TRIGEN PROXIMAL STRAIGHT HUMERAL NAIL 8/7 X 16 recall (Smith & Nephew, Inc.)
Medical deviceClass IIReported June 24, 2026 · Humeral nail due to a manufacturing error is missing distal holes and if implanted may lead to revision surgery but, if the missing holes are identified before... - Park St. Deli Macaroni & Cheese recall (BEF Foods, Inc)
FoodClass IIReported June 17, 2026 · Undeclared allergen (soy lecithin). - Hintermann Series Talar Implant recall (DT MedTech, LLC)
Medical deviceClass IIReported June 17, 2026 · Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant... - Yunker recall (Sato Pharmaceutical Inc.)
FoodClass IIIReported June 10, 2026 · Product does not meet label claim for Vitamin E. - ARTIS Icono biplane recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported June 10, 2026 · During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during... - ARTIS pheno recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported June 10, 2026 · During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during... - Oncology Kit w/60" recall (ICU Medical, Inc.)
Medical deviceClass IIReported May 27, 2026 · Oncology sets/closed system transfer devices with extension sets may leak resulting in therapy delayed if noticed and corrected during setup, but if the leak... - Tangent Endoscopy recall (TANGENT ENDOSCOPY, LLC)
Medical deviceClass IIReported May 27, 2026 · Affected devices exhibited fractures at the distal shaft tip without complete detachment. - Alain MILLIAT recall (FINESALER LLC)
FoodClass IIReported May 20, 2026 · Product may contain foreign objects, specifically glass. - Buprenorphine Hydrochloride recall (ENDO USA, Inc.)
DrugClass IIReported May 20, 2026 · Crystallization; identified as Buprenorphine free base - Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO recall (Edwards Lifesciences, LLC)
Medical deviceClass IIReported May 20, 2026 · Labeling update to provide warning if functionality of the valve replacement delivery system is compromised. - Philips Azurion. System Code Description recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported May 20, 2026 · Potential for the bolts and plastic parts of the Cable Hose Carriers that hold the cable hose to the monitor ceiling suspension may loosen and/or break over... - Revolution Apex Select recall (GE Medical Systems, LLC)
Medical deviceClass IIReported May 20, 2026 · GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used... - Revolution Apex recall (GE Medical Systems, LLC)
Medical deviceClass IIReported May 20, 2026 · GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used... - Revolution CT ES recall (GE Medical Systems, LLC)
Medical deviceClass IIReported May 20, 2026 · GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used... - Revolution Apex Plus recall (GE Medical Systems, LLC)
Medical deviceClass IIReported May 20, 2026 · GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used... - Revolution Apex Elite recall (GE Medical Systems, LLC)
Medical deviceClass IIReported May 20, 2026 · GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used... - Revolution CT recall (GE Medical Systems, LLC)
Medical deviceClass IIReported May 20, 2026 · GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used... - Revolution Ascend recall (GE Medical Systems, LLC)
Medical deviceClass IIReported May 20, 2026 · GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - 1. 3 VALVE MAN KIT recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - 1. DBD-MTS recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Namic Preceptor Manifold recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Namic Preceptor Manifold recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Namic Angiographic Manifold recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Namic Angiographic Manifold recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Namic Angiographic Manifold recall (Medline Industries, LP)
Medical deviceClass IReported May 20, 2026 · Medline has identified the presence of particulate within the fluid path of the Manifolds. - Brand Name: DONJOY Product Name: ICEMAN recall (DJO, LLC)
Medical deviceClass IIReported May 20, 2026 · Due to broken connector which may result in a temporary interruption of prescribed cold therapy. - Brand Name: DONJOY Product Name: ICEMAN W/ recall (DJO, LLC)
Medical deviceClass IIReported May 20, 2026 · Due to broken connector which may result in a temporary interruption of prescribed cold therapy. - Brand Name: DONJOY Product Name: ICEMAN W/ recall (DJO, LLC)
Medical deviceClass IIReported May 20, 2026 · Due to broken connector which may result in a temporary interruption of prescribed cold therapy. - Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 ... recall (DJO, LLC)
Medical deviceClass IIReported May 20, 2026 · Due to broken connector which may result in a temporary interruption of prescribed cold therapy. - Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028 recall (Omnicell, Inc.)
Medical deviceClass IReported May 20, 2026 · Potential for mislabeled syringe produced by the i.v.STATION device. - Horizon Organic Chocolate Organic Lowfat Milk. Saleable Unit recall (Horizon Organic Dairy, LLC)
FoodClass IIReported May 13, 2026 · Package integrity compromised. - SunRidge Farms Organic SUNSET SOUP MIX CERTIFIED ORGANIC BY QAI recall (Falcon Trading Co., Inc.)
FoodClass IIIReported May 13, 2026 · Potential contamination with pesticides, haloxyfop and thiamethoxam - SunRidge Farms Organic CHILI BEAN BLEND CERTIFIED ORGANIC BY QAI recall (Falcon Trading Co., Inc.)
FoodClass IIIReported May 13, 2026 · Potential contamination with pesticides, haloxyfop and thiamethoxam - SunRidge Farms Organic Black Beans CERTIFIED ORGANIC BY QAI recall (Falcon Trading Co., Inc.)
FoodClass IIIReported May 13, 2026 · Potential contamination with pesticides, haloxyfop and thiamethoxam - MILK-N-EGG MIX recall (Griffith Foods Inc.)
FoodClass IReported May 13, 2026 · Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella. - MILK WASH recall (Griffith Foods Inc.)
FoodClass IReported May 13, 2026 · Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella. - Costco Service Deli Department 63 MEATLOAF SEASONING MORE FLV Pack Size: 4-5lb. Bags... recall (Griffith Foods Inc.)
FoodClass IReported May 13, 2026 · Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella. - Montebianco recall (Disaronno Ingredients S.p.a.)
FoodClass IIReported May 13, 2026 · Undeclared allergen Milk. The presence of the milk allergen in the product was found to exceed acceptable levels despite the product being labeled with the... - Christopher Ranch Peeled Garlic 6 oz. recall (Tops Markets LLC)
FoodClass IIIReported May 13, 2026 · The potential contamination with Clostridium botulinum, due to risk of temperature abuse during chilled storage at the firm - Garland Fresh Peeled Garlic 6 oz. bag recall (Tops Markets LLC)
FoodClass IIIReported May 13, 2026 · The potential contamination with Clostridium botulinum, due to risk of temperature abuse during chilled storage at the firm - ZENBONE recall (Orthorebirth Co Ltd)
Medical deviceClass IIReported May 13, 2026 · Resorbable bone void filler falls outside standard specifications. - BioCera Fibers recall (Orthorebirth Co Ltd)
Medical deviceClass IIReported May 13, 2026 · Resorbable bone void filler falls outside standard specifications. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Ophthalmic Tissue Forceps (DEX") are sterile, hand-held ophthalmic surgical instruments designed for grasping, manipulating, compressing, pulling, or joining... - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - ERBEFLO 2 recall (Erbe Medical, LLC)
Medical deviceClass IIReported May 13, 2026 · Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible... - ERBEFLO CleverCap: Hybrid Tubing/Cap Set for Olympus Scopes recall (Erbe Medical, LLC)
Medical deviceClass IIReported May 13, 2026 · Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible... - ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources recall (Erbe Medical, LLC)
Medical deviceClass IIReported May 13, 2026 · Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible... - Brand Name: Spacelabs Ultraview SL Command Module Product Name: SL Command Module ... recall (Spacelabs Healthcare, Inc.)
Medical deviceClass IIReported May 13, 2026 · Due to a manufacturing issue (i.e. malfunctioning of electrical Leakage tester). - Prodisc C SK U.S. IMPLANT EXTRA LARGE 6MM. Model Number: PDSXL6. Total cervical... recall (Centinel Spine, Inc.)
Medical deviceClass IIReported May 13, 2026 · Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was... - Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc... recall (Centinel Spine, Inc.)
Medical deviceClass IIReported May 13, 2026 · Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was... - LUX-Dx II Plus recall (Boston Scientific Corporation)
Medical deviceClass IIReported May 13, 2026 · For some patients upgraded from a LUX-Dx M301 device to a new Model M302 or M312, the new ICM device is not collecting PVC Burden data (both M302/M312) or... - LUX-DX II recall (Boston Scientific Corporation)
Medical deviceClass IIReported May 13, 2026 · For some patients upgraded from a LUX-Dx M301 device to a new Model M302 or M312, the new ICM device is not collecting PVC Burden data (both M302/M312) or... - Medical Action Industries Inc. Pack Cath BHH recall (Medical Action Industries, Inc. 306)
Medical deviceClass IReported May 13, 2026 · Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the... - Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating... recall (American Contract Systems Inc)
Medical deviceClass IReported May 13, 2026 · Impacted kits contain syringes recalled by Medline Industries. Syringe rotating adaptor may unwind during use, which may result in a loose connection or full... - Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard PERC TRAY kit. Model Numbers: SLPC34-01 recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard NEURO IR PERIPHERAL recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard HEART CATH recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CATH LAB kit. Model Number: SACL75-01. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CATH LAB kit. Model Number: SACL75AM. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04 recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05 recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - VOCSN V+Pro package recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported May 13, 2026 · Respiratory system intended to provide continuous/intermittent ventilator support, may not have been evaluated under all intended high-pressure conditions... - Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06 recall (Intuitive Surgical, Inc.)
Medical deviceClass IReported May 13, 2026 · Reloads for curved-tipped stapler may potentially produce an incomplete staple line. - Top Lid Label: Einstein Bros Bagels Honey Almond Double-Whipped Shmear. Cup Label: ... recall (Schreiber Foods Inc)
FoodClass IIReported May 6, 2026 · Undeclared allergen (almond). - Medline and Centurion medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal... - Centurion medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal... - Medline or Centurion medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal... - Centurion medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal... - Medline and Centurion medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal... - Centurion medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market...