Recalls in December 2025 (page 2)
421 recalls.
- AXIOS Stent and Electrocautery-Enhanced Delivery System - 20mm x 10mm recall (Boston Scientific Corporation)
Medical deviceClass IReported February 11, 2026 · Increased reports of stent deployment and expansion issues. The most common outcome reasonably foreseeable resulting from difficulty deploying the stent is... - Goldenroot Yuzu Ginger Lemongrass Ginger Beer. 12 oz. recall (Weaver's Brew LLC)
FoodClass IIReported February 4, 2026 · Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process. - Goldenroot Lemon Ginger Jalapeno Ginger Beer. 12 oz. recall (Weaver's Brew LLC)
FoodClass IIReported February 4, 2026 · Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process. - Goldenroot Lemon Ginger Hibiscus Ginger Beer. 12 oz. recall (Weaver's Brew LLC)
FoodClass IIReported February 4, 2026 · Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process. - Goldenroot Lemon Double Ginger recall (Weaver's Brew LLC)
FoodClass IIReported February 4, 2026 · Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process. - Goldenroot Lemon Ginger Elderberry Ginger Beer. 12 oz. recall (Weaver's Brew LLC)
FoodClass IIReported February 4, 2026 · Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process. - Roasted Green Chile & Jack Cheese Tamales Ingredients: Organic Corn Flour Masa recall (Prima Vera Nueva, Inc.)
FoodClass IIReported February 4, 2026 · Potential contamination with biological hazards (Listeria monocytogenes). - Black Bean Bonanza Tamales with Black Beans and Jack Cheese Ingredients: Organic Corn... recall (Prima Vera Nueva, Inc.)
FoodClass IIReported February 4, 2026 · Potential contamination with biological hazards (Listeria monocytogenes). - Butternut Squash Tamales with Roasted Green Chiles recall (Prima Vera Nueva, Inc.)
FoodClass IIReported February 4, 2026 · Potential contamination with biological hazards (Listeria monocytogenes). - Roasted Green Chile Tamales NO DAIRY Ingredients: Organic Corn Flour Masa recall (Prima Vera Nueva, Inc.)
FoodClass IIReported February 4, 2026 · Potential contamination with biological hazards (Listeria monocytogenes). - Black Bean Bonanza Tamales with Black Beans NO DAIRY Ingredients: Organic Corn Flour Masa recall (Prima Vera Nueva, Inc.)
FoodClass IIReported February 4, 2026 · Potential contamination with biological hazards (Listeria monocytogenes). - BBQ Chipotle Bean & White Cheddar Tamales Ingredients: Organic Corn Flour Masa recall (Prima Vera Nueva, Inc.)
FoodClass IIReported February 4, 2026 · Potential contamination with biological hazards (Listeria monocytogenes). - Mushroom recall (Prima Vera Nueva, Inc.)
FoodClass IIReported February 4, 2026 · Potential contamination with biological hazards (Listeria monocytogenes). - Roasted Pumpkin & White Cheddar Tamales Ingredients: Organic Corn Flour Masa recall (Prima Vera Nueva, Inc.)
FoodClass IIReported February 4, 2026 · Potential contamination with biological hazards (Listeria monocytogenes). - Mushroom recall (Prima Vera Nueva, Inc.)
FoodClass IIReported February 4, 2026 · Potential contamination with biological hazards (Listeria monocytogenes). - Butternut Squash Tamales With Roasted Green Chiles recall (Prima Vera Nueva, Inc.)
FoodClass IIReported February 4, 2026 · Potential contamination with biological hazards (Listeria monocytogenes). - HIGHER HARVEST by H-E-B brand recall (Plant Based Innovations, LLC)
FoodClass IIReported February 4, 2026 · Contains undeclared Almonds - McCafe Premium Roast Decaf Coffee K-Cup Pods recall (Keurig DR Pepper, Inc.)
FoodClass IIReported February 4, 2026 · Product is labeled as decaf, but might contain caffeine. - Qunol recall (QUTEN RESEARCH INSTITIUTE LLC)
FoodClass IIReported February 4, 2026 · Mold contamination detected for raw material lots that were produced in July and used in finished goods. - SOMA KITCHEN NATURAL ASAFOETIDA Net Wt. 4 oz recall (BHARAT BAZAR)
FoodClass IIReported February 4, 2026 · Undeclared wheat. - Glycopyrrolate Oral Solution recall (NOVADOZ PHARMACEUTICALS LLC)
DrugClass IIIReported February 4, 2026 · Failed Impurities/Degradation Specifications - INON ACE Antacid tablets recall (Sato Pharmaceutical Co., Ltd)
DrugClass IIReported February 4, 2026 · Failed Disintegration Specifications: above the time expected. - parodontax recall (Haleon US Holdings LLC)
DrugClass IIIReported February 4, 2026 · Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing or illegible lot and expiration date coding on the bottles. - Sterile Water for Irrigation recall (Baxter Healthcare Corporation)
DrugClass IIReported February 4, 2026 · Presence of particulate matter: plastic particles from the bottle rim were observed floating into the solution - BEAR Implant. Model Number: 1000. recall (Miach Orthopaedics)
Medical deviceClass IIReported February 4, 2026 · 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... - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported February 4, 2026 · BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators. - Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23 recall (LimFlow, Inc.)
Medical deviceClass IIReported February 4, 2026 · Incorrect expiration date - SmartPath to dStream for XR and 3.0T. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - SmartPath to dStream for 3.0T. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Upgrade to MR 7700. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - MR 7700. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia Elition X. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia Elition S. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia Ambition X. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia Ambition S. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia 3.0T CX. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia 3.0T. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia 1.5T. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Evolution Upgrade 3.0T. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Evolution Upgrade 1.5T. Product Codes recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Chest Drainage Units and Accessories: Product Code Description 1.... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported February 4, 2026 · The firm is updating the IFU to clarify the intended patient population for the identified chest drainage units and accessories as adults, 18 years and older.... - Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet Systems... recall (Zimmer Surgical Inc)
Medical deviceClass IIReported February 4, 2026 · Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or... - Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems... recall (Zimmer Surgical Inc)
Medical deviceClass IIReported February 4, 2026 · Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or... - Medline medical procedure convenience kits labeled as: 1) WATKINS SPINE PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) C-SECTION PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: CIRCUMCISION PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) RR-GYN LAPAROSCOPY PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) DEPAUL BASIC NEURO-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) INPATIENT CTRL LN DRG CHG recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: HEAD SHAVE-LATEX SAFE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) DRAWER 1 AIRWAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) MEM MAXILLOFACIAL PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) SMJ LAP CHOLE PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) MIDDLE EAR CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) BREAST-HERNIA-PORT CDS-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) PACER / CATH LAB PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) CATH LAB PACEMAKER PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: NERVE BLOCK TRAY 2 recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Conductivity Standard Solution Catalog/Model Numbers: 10001 recall (NIPRO Technical Services, Inc.)
Medical deviceClass IIReported February 4, 2026 · due to a defect associated with the conductivity values of the solution used to calibrate meters and result in the reporting of incorrect conductivity values... - PREGNANCY TEST 24CT recall (GOLD STAR DISTRIBUTION INC)
Medical deviceClass IIReported February 4, 2026 · Potential exposure of rodents and rodent activity in the distribution center. - Toothbrushes recall (GOLD STAR DISTRIBUTION INC)
Medical deviceClass IIReported February 4, 2026 · Potential exposure of rodents and rodent activity in the distribution center. - Feminine hygiene products recall (GOLD STAR DISTRIBUTION INC)
Medical deviceClass IIReported February 4, 2026 · Potential exposure of rodents and rodent activity in the distribution center. - Condoms recall (GOLD STAR DISTRIBUTION INC)
Medical deviceClass IIReported February 4, 2026 · Potential exposure of rodents and rodent activity in the distribution center. - Bandages and first aid kits: FIRST AID KIT 24/42PC recall (GOLD STAR DISTRIBUTION INC)
Medical deviceClass IIReported February 4, 2026 · Potential exposure of rodents and rodent activity in the distribution center. - Alphenix INFX-8000V recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported February 4, 2026 · It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray... - Alphenix INFX-8000H recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported February 4, 2026 · It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray... - Alphenix INFX-8000F recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported February 4, 2026 · It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray... - Alphenix INFX-8000C recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported February 4, 2026 · It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray... - Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 4, 2026 · Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a... - Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 4, 2026 · Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a... - AlternatiV+ Screw-In Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - AlternatiV+ Max Knotless Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - Genesis Push-In Suture Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - Genesis Knotless Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - Genesis Dual Thread Screw-In Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - Genesis Screw-In Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - Fixone Biocomposite Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - Fixone Hybrid Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft recall (Cerapedics, Inc.)
Medical deviceClass IIReported February 4, 2026 · Incorrect expiration date - Brand Name: Elekta Medical Linear Accelerator Product Name: Elekta Synergy recall (Elekta, Inc.)
Medical deviceClass IIReported February 4, 2026 · Due to a manufacturing issue and electrical grounding of systems. - Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER Model/Catalog... recall (SunMed Holdings, LLC)
Medical deviceClass IReported February 4, 2026 · Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine. - Brand Name: Broselow Product Name: Broselow Domestic Complete ALS Organizer ... recall (SunMed Holdings, LLC)
Medical deviceClass IReported February 4, 2026 · Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine. - Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape ... recall (SunMed Holdings, LLC)
Medical deviceClass IReported February 4, 2026 · Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine. - Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape ... recall (SunMed Holdings, LLC)
Medical deviceClass IReported February 4, 2026 · Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine. - Cuban Crackers Galletas Cubanas recall (Lily's Bakery Factory)
FoodClass IIReported January 28, 2026 · Undeclared colors FD&C yellow #5, FD&C yellow #6, and FD&C red 40 - MEAL SIMPLE RED LENTIL DAL SOUP recall (Bakkavor)
FoodClass IIReported January 28, 2026 · Undeclared Milk. Wrong product in container. - White Castle Original Sliders recall (White Castle System)
FoodClass IReported January 28, 2026 · Undeclared allergens (milk and soy). - Mini Gaceniga Authentic Cuban Loaf Cake Classic recall (CATAO MARKET LLC)
FoodClass IIReported January 28, 2026 · Undeclared colors FD&C Yellow #5 - Mini Gaceniga Authentic Cuban Loaf Cake Raisins recall (CATAO MARKET LLC)
FoodClass IIReported January 28, 2026 · Undeclared colors FD&C Yellow #5 - Gaceniga Authentic Cuban Loaf Cake Raisins recall (CATAO MARKET LLC)
FoodClass IIReported January 28, 2026 · Undeclared colors FD&C Yellow #5 - Gacen¿iga Authentic Cuban Loaf Cake Classic recall (CATAO MARKET LLC)
FoodClass IIReported January 28, 2026 · Undeclared colors FD&C Yellow #5 - All human food products distributed from the firm. Including but not limited to: ... recall (GOLD STAR DISTRIBUTION INC)
FoodClass IIReported January 28, 2026 · Potential exposure of rodents and rodent activity in the distribution center. - Gregory's Foods Bag Full of Cookies recall (Gregory's Foods, Inc)
FoodClass IReported January 28, 2026 · Undeclared peanuts. - Australian Greenlip Abalone recall (Southern Rocklobster LTD USA)
FoodClass IIReported January 28, 2026 · Potential Listeria Monocytogenes contamination - Icosapent Ethyl capsules recall (Zydus Pharmaceuticals (USA) Inc)
DrugClass IIReported January 28, 2026 · Subpotent Drug: Due to oxidation caused by leakage of the contents of the capsules - Diclofenac Sodium Topical Gel recall (Cipla USA, Inc.)
DrugClass IIIReported January 28, 2026 · Failed PH Specifications - Patient Information Center iX recall (Philips North America)
Medical deviceClass IIReported January 28, 2026 · A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system. - Rifton Equipment recall (Community Products, LLC)
Medical deviceClass IIReported January 28, 2026 · Potential for fraying on the body support strap. - Rifton Equipment recall (Community Products, LLC)
Medical deviceClass IIReported January 28, 2026 · Potential for fraying on the body support strap. - Rifton Equipment recall (Community Products, LLC)
Medical deviceClass IIReported January 28, 2026 · Potential for fraying on the body support strap.