Safety Recalls
RSS ↗15,186 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 2,601–2,650 of 15,186
- Class II
Medical Device Recall · January 7, 2026
Medline Convenience Kits: 1) HYSTEROSCOPY, Model Number: CDS984086I; 2) KIT GYN ONCOLOGY LAP, Model Number: DYKMBNDL91A; 3) VAGINAL HYSTERECTOMY PACK-LF, Model Number: DYNJ0373807J; 4) VAGINALMedline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- Class II
Medical Device Recall · January 6, 2026
PRISMAFLEX ST150 SET US, Product Code 107640US; Dialyzer, High Permeability With Or Without Sealed Dialysate SystemThere is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
- Class III
Medical Device Recall · January 6, 2026
WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POMThe mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown.
- Class I
Food Recall · January 6, 2026
Carrot Top Kitchens Lemon & Garlic Hummus; contains chickpeas, tahini, lemon juice & zest, garlic, salt; 8 oz.Contains undeclared sesame
- Class II
Food Recall · January 6, 2026
Karison brand ALSI PINNI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Sugar Flax Seeds, Almonds, Zero Trans Fat, Vegetable Shortening; UPC: 8 97307 00251 2; Distributed By: Karison Foods & SnackProduct contains milk, which is undeclared in the ingredient statement.
- Class II
Food Recall · January 6, 2026
Karison brand PANJIRI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Almonds, Sugar, Lotus Seeds, Fennel Seeds, Flax Seeds, Edible Gum, Ginger Powder, Zero Trans Fat Vegetable Shortening; UPC: 8 9Product contains milk, which is undeclared in the ingredient statement.
- Class I
Food Recall · January 6, 2026
Carrot Top Kitchens Cherry Pepper Hummus; contains chickpeas, tahini, pickled cherry peppers, vinegar, garlic, salt; 8 oz.Contains undeclared sesame
- Class I
Food Recall · January 6, 2026
HerbsForever- Gastro Care; Ayruvedic Herbal Supplement; 90 VEGE Capsules; Extract 800 MG each capsule. UPC: 8 07814 00124 3Potential undeclared allergen ingredient (Wheat)
- Class II
Medical Device Recall · January 6, 2026
PRIMSAFLEX M100 SET, Product Code 106697; Dialyzer, High Permeability With Or Without Sealed Dialysate SystemThere is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
- Class II
Drug Recall · January 6, 2026
AQ 120 GFEW, Aquarion Preserved Cartridges (2) 3.7 Gallons eachcGMP deviations.
- Class II
Medical Device Recall · January 6, 2026
PRISMAFLEX HF1000 SET, Product Code 107142; Dialyzer, High Permeability With Or Without Sealed Dialysate SystemThere is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
- Class II
Medical Device Recall · January 6, 2026
PRISMAFLEX HF1000 SET, Product Code 107140; Dialyzer, High Permeability With Or Without Sealed Dialysate SystemThere is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
- Class I
Food Recall · January 6, 2026
Carrot Top Kitchens White Truffle Hummus; contains chickpeas, tahini, truffle oil, lemon, salt; 8 oz.Contains undeclared sesame
- Class II
Food Recall · January 6, 2026
Karison brand NO SUGAR ADDED BESAN LADDOO; Ingredients: Gram Flour, Butter, Zero Trans Fat Vegetable Shortening (Hydrogenated Soybean Oil), Pistachio, Almonds, Sweetener with Nutrasweet; UPC: 8 97397Product contains milk, which is undeclared in the ingredient statement.
- Class I
Food Recall · January 6, 2026
Carrot Top Kitchens Lime Ginger Hummus; contains chickpeas, tahini, fresh ginger, lime juice & zest, salt; 8 oz.Contains undeclared sesame
- Class II
Medical Device Recall · January 6, 2026
PRISMAFLEX ST100 SET US, Product Code 107636US; Dialyzer, High Permeability With Or Without Sealed Dialysate SystemThere is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
- Class II
Food Recall · January 6, 2026
Karison brand BESAN LADDOO; NET WT. 12 oz.; Ingredients: Gram Flour, Butter, Sugar, Zero Trans Fat Vegetable Shortening, Almonds, Cardamom; UPC: 8 9730700240 6; Distributed By: Karson Foods & Snacks IProduct contains milk, which is undeclared in the ingredient statement.
- Class I
Food Recall · January 6, 2026
Carrot Top Kitchens Sundried Tomato and Caper Hummus; contains chickpeas, sundried tomatoes, tahini, capers, vinegar, salt; 8 oz.Contains undeclared sesame
- Class II
Food Recall · January 6, 2026
Karison brand PUNJABI PINNI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Sugar, Almonds, Zero Trans Fat, Vegetable Shortening; UPC: 8 97307 00215 4; Distributed By: Karison Foods & Snacks Inc.,Product contains milk, which is undeclared in the ingredient statement.
- Class I
Food Recall · January 6, 2026
HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4Potential undeclared allergen ingredient (Wheat)
- Class II
Medical Device Recall · January 6, 2026
PRISMAFLEX TPE2000 SET, Product Code 114093; Dialyzer, High Permeability With Or Without Sealed Dialysate SystemThere is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
- Class II
Medical Device Recall · January 6, 2026
OXIRIS SET, Product Code 112016; Dialyzer, High Permeability With Or Without Sealed Dialysate SystemThere is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
- Class II
Medical Device Recall · January 6, 2026
PRISMAFLEX M150 SET, Product Code 109990; Dialyzer, High Permeability With Or Without Sealed Dialysate SystemThere is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
- Class II
Medical Device Recall · January 5, 2026
Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION, Model Number: DYKM1361A; 2) TRUNK KIT 1EA, Model Number: DYKM2013; 3) TRUNK KIT 1EA, Model Number: DYKM2013A; 4) RN TRUNK KIT, Model Number:Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
- Class II
Medical Device Recall · January 5, 2026
Medline Convenience Kits: 1) NAIL KIT, Model Number: POD14214Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
- Class II
Medical Device Recall · January 5, 2026
VITEK 2 Gram-negative Susceptibility Cards Containing o Polymyxin B (pb02n) o Ceftazidime/avibactam (cza02n) o Meropenem/Vaborbactam (mev01n) o Imipenem (ipm05n) o Imipenem/Relebactam (ipr01n); CARDPotential risk of Quality Control failures and/or false resistant antibiotic results when testing isolates of Enterobacterales/Enterobacteriaceae species and/or Pseudomonas aeruginosa with the identified antibiotic formulations. Issue may lead to QC failure or false resistant results.
- Class II
Medical Device Recall · January 5, 2026
Medline Sterile Saline Wound Wash, Cleansing & Wound Irrigation, USP Normal Saline (0.9% Sodium Chloride), 7.1 FL OZ (210 mL), DBD-CAN,SPRAY,7.1-OZ,SALINE,WOUND WASH,S, Model Number MDSALINE7Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
- Unclassified
Vehicle Recall · January 5, 2026
2025 MERCEDES-BENZ GLC 350 E 4MATIC, 2025 MERCEDES-BENZ E 350, 2025 MERCEDES-BENZ E 350 4MATIC, 2025 MERCEDES-BENZ GLC 300, 2025 MERCEDES-BENZ C 300, 2025 MERCEDES-BENZ GLC 300 4MATIC, 2025 MERCEDES-BAn instrument panel display that fails to show critical safety information, such as the speedometer and warning lights, increases the risk of a crash.
- Class II
Medical Device Recall · January 5, 2026
Medline Convenience Kits: 1) NAIL KIT, Model Number: DYKM1528Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
- Class II
Medical Device Recall · January 5, 2026
EMPOWR Acetabular System: Liner, 10 degree Hooded, HXe+, 36H, REF: 942-01-36H; Liner, 10 degree Hooded, HXe+, 36J, REF: 942-01-36J; Liner, 10 degree Hooded, HXe+, 40G, REF: 942-01-40G; Liner, 10 degr942-01-40G acetabular system package was found to contain 942-01-36H acetabular system; and several other acetabular system and knee insert devices may also have a packaging discrepancy, which may cause surgical delay to exchange devices or revision surgery.
- Class II
Medical Device Recall · January 5, 2026
EMPOWR 3D Knee Tibial Insert 5R 14MM, VE, REF: 342-14-705942-01-40G acetabular system package was found to contain 942-01-36H acetabular system; and several other acetabular system and knee insert devices may also have a packaging discrepancy, which may cause surgical delay to exchange devices or revision surgery.
- Class II
Medical Device Recall · January 5, 2026
Raz-AT (Attendant Tilt) Mobile Shower Commode Chair, Catalog Number Z300 UDI-DI code: (01)00628758003007 Raz-ART (Attendant Rotational Tilt) Mobile Shower Commode Chair, Catalog Number Z333 UDI-DDue to a modification by a vendor and may be reinstalled without properly engaging the outside rear seat brackets that are used to keep the seat in place.
- Class II
Medical Device Recall · January 5, 2026
Meijer STERILE saline wound wash, First Aid Cleansing Spray, 0.9% USP SODIUM CHLORIDE, 7.1FL OZ (210 mL), DBD-CAN,SPRAY,7.1-OZ,SALINE,WOUND WASH,S, Model Number MJSALINE7Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
- Unclassified
Vehicle Recall · January 4, 2026
2025 VOLVO VNL (4), 2026 VOLVO VNL (4)Turn signals that do not function properly may fail to indicate the driver's intention to change vehicle direction, increasing the risk of a crash.
- Unclassified
Vehicle Recall · January 4, 2026
Volkswagen Group of America, Inc.
2026 AUDI Q3Closing the sunroof without the ability to see it can increase the risk of injury to occupants.
- Class II
Medical Device Recall · January 2, 2026
ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 266-01-000-10-N UDI-DI code: 00190376476179; GMDN 12844 The ATEC Navigation Disc Prep Instruments are intended for use inDue a design issue where the navigated array connection geometry is incorrect.
- Class II
Drug Recall · January 2, 2026
Lanreotide Injection, 120 mg/0.5 mL, 0.5 mL per pre-filled syringe, For deep subcutaneous injection, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059.Presence of Particulate Matter.
- Class II
Medical Device Recall · January 2, 2026
Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.Tyvek bag seal issue which may compromise sterility of the kit.
- Class II
Medical Device Recall · January 2, 2026
ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 267-01-000-10-N UDI-DI code: 00190376541471; GMDN 12844 The ATEC Navigation Disc Prep Instruments are intended for use inDue a design issue where the navigated array connection geometry is incorrect.
- Class II
Medical Device Recall · December 31, 2025
Medica Capillary Tubes; EasyBloodGas/EasyStat Capillary Tube Kit.A systematic positive bias of up to 20% was identified across the reportable potassium range, resulting in false elevation results of patient samples when using Medica s capillary tubes.
- Class II
Medical Device Recall · December 31, 2025
Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN SET,60DRP,1NEEDLE-FREE VALV, Model Number: DYNDTB0529; 2) IV ADMIN SET, 10DRP, 1NF, 92, Model Number: DYNDTB1029; 3) DBD-IUnder circumstances involving exposure to particular chemicals and mechanical forces, the male luer connectors for the specified IV Administration and Extension sets may leak, crack, and/or break during use, which may result in a delay in patient treatment, blood loss, infection, an air embolism, and/or underdosage of medication.
- Class II
Drug Recall · December 31, 2025
Wizcure Pharmaa Private Limited
Vista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops Advanced Dry Eye Relief Revitalizing Formula, 10 ml (1/3 fl.oz.), Wizcure Pharmaa PVT. LTD., H-881, Phase 3, RIICO Industrial Area, Bhiwadi-301019Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
- Class II
Drug Recall · December 31, 2025
Wizcure Pharmaa Private Limited
BioGlo Fluorescein Sodium Ophthalmic Strips USP, 100 diagnostic strips, Manufactured by Omni Lens PVT. Ltd., 5 - Samrudhhi, Opp. Sakar-III, Navrangpura, Ahmedabad, Gujarat, India - 380014, Email:info@Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
- Class II
Drug Recall · December 31, 2025
Wizcure Pharmaa Private Limited
Vista Gonio Eye Lubricant, Hypromellose Ophthalmic Solution USP (Sterile Drops. Dry Eye Relief, 15 ml. (1/2 fl. oz.), Wizcure Pharmaa Pvt. Ltd., H-881, Phase-3, RIICO Industrial Area, Bhiwadi-901019,Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
- Class II
Medical Device Recall · December 31, 2025
BEAR Implant. Model Number: 1000.Incorrect expiration date on label that extends beyond the product's documented/approved shelf life. With an incorrect expiration date, the UDI will also be incorrect.
- Class II
Drug Recall · December 31, 2025
Wizcure Pharmaa Private Limited
Vista Tears Polyethylene Glycol 400 0.4% w/v, Propylene Glycol 0.3% w/v Eye Drops, Dry Eye Relief, Lubricant Drops, Sterile 10 ml (1/3 fl. oz.), Manufactured by: RA/Drugs/ MFG/2019/196283, Omni Lens PLack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
- Class II
Drug Recall · December 31, 2025
Wizcure Pharmaa Private Limited
CHNaO Fluorescein Sodium Ophthalmic Strips, USP 1mg, packaged as a) 100-count box, NDC 83851-100-10; b) 300-count box, NDC 83851-100-30. Manufactured by Wizcure Pharmaa PVT. LTD, H-681, Phase 3, RIICLack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
- Class II
Drug Recall · December 31, 2025
Levothyroxine Sodium Tablets, USP, Thyro-Tabs, 150mcg, 1000 Tablets, Rx only, Manufactured by: LLOYD, Inc., Shenandoah, IA, 51601 USA, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058 USA, NDC: 477Product Mix-Up: A single bottle of this lot was reported by a pharmacy to contain 88 mcg tablets instead of 150 mcg tablets.
- Class II
Medical Device Recall · December 31, 2025
Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software Version: N/A Product Description: Total cervical disc replacement Component: NoProducts were mislabeled as the 6mm product but included the 5 mm product.
- Class II
Drug Recall · December 31, 2025
Wizcure Pharmaa Private Limited
Bio Glo Fluorescein Sodium Ophthalmic Strips USP, 300 diagnostic strips, Manufactured Omni Lens Pvt Ltd 5 - Samruddhi, Opp. Sakar - III, Navrangpura, Ahmedabad - 380014, India, Email:info@omnilens.inLack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.