Recalls in January 2026 (page 4)

471 recalls.

• Testosterone 200mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• Testosterone 100mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• Testosterone 75mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• Testosterone 100mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
  DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter
• Doxazosin Tablets recall (Unichem Pharmaceuticals USA Inc.)
  DrugClass IIIReported February 18, 2026 · Tablets/Capsules Imprinted with Wrong ID
• Azurion 5 M20 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
• Azurion 5 M12 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
• Azurion 7 M20 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
• Azurion 7 M12 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
• Azurion 7 B20 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
• Azurion 7 B12 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
• Azurion 3 M15 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
• Azurion 3 M12 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
• ATEC Lateral Navigation Disc Prep Instruments LIF NAV recall (Alphatec Spine, Inc.)
  Medical deviceClass IIReported February 18, 2026 · Due a design issue where the navigated array connection geometry is incorrect.
• ATEC Lateral Navigation Disc Prep Instruments LIF NAV recall (Alphatec Spine, Inc.)
  Medical deviceClass IIReported February 18, 2026 · Due a design issue where the navigated array connection geometry is incorrect.
• Laerdal Compact Suction Unit 4 RTCA version recall (Laerdal Medical Corporation)
  Medical deviceClass IIReported February 18, 2026 · units manufactured in a limited time period may emit electromagnetic noise beyond the acceptable limits for RTCA application specified in RTCA DO-160G Chapter...
• Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01. recall (AVID Medical, Inc.)
  Medical deviceClass IIReported February 18, 2026 · Tyvek bag seal issue which may compromise sterility of the kit.
• WB Impression Post Closed Tray incl. guide screw recall (Straumann USA LLC)
  Medical deviceClass IIIReported February 18, 2026 · The mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown.
• Spectral CT 7500 on Rails recall (Philips North America Llc)
  Medical deviceClass IIReported February 18, 2026 · As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners...
• Spectral CT recall (Philips North America Llc)
  Medical deviceClass IIReported February 18, 2026 · As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners...
• IQon Spectral CT recall (Philips North America Llc)
  Medical deviceClass IIReported February 18, 2026 · As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners...
• Brilliance iCT recall (Philips North America Llc)
  Medical deviceClass IIReported February 18, 2026 · As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners...
• Product is Frozen Half Shell Oysters in 15-16 pound blocks. Packaged in generic brown... recall (Khee Trading, Inc.)
  FoodClass IIReported February 11, 2026 · Imported oysters potentially contaminated with Norovirus
• Bread Crumbs recall (VH FOODS INC)
  FoodClass IReported February 11, 2026 · Undeclared allergens: egg and milk
• Sea Moss Gel Superfood recall (Diva Fam Inc)
  FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination
• Sea Moss Gel Superfood recall (Diva Fam Inc)
  FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination
• Sea Moss Gel Superfood recall (Diva Fam Inc)
  FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination
• Sea Moss Gel Superfood recall (Diva Fam Inc)
  FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination
• Sea Moss Gel Superfood recall (Diva Fam Inc)
  FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination
• Sea Moss Gel Superfood recall (Diva Fam Inc)
  FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination
• Sea Moss Gel Superfood recall (Diva Fam Inc)
  FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination
• Sea Moss Gel Superfood recall (Diva Fam Inc)
  FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination
• Sea Moss Gel Superfood recall (Diva Fam Inc)
  FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination
• Sea Moss Gel Superfood recall (Diva Fam Inc)
  FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination
• Sea Moss Gel Superfood recall (Diva Fam Inc)
  FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination
• Sea Moss Gel Superfood recall (Diva Fam Inc)
  FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination
• Sea Moss Gel Superfood recall (Diva Fam Inc)
  FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination
• Sea Moss Gel Superfood recall (Diva Fam Inc)
  FoodClass IIReported February 11, 2026 · potential Clostridium botulinum contamination
• spicely ORGANIC sumac NO ARTIFICIAL COLORING NO GLUTEN - NO MSG - NO SOY NO... recall (Organic Spices, Inc)
  FoodClass IIReported February 11, 2026 · Product contains salt and is mislabeled
• spicely ORGANIC celery salt NO ARTIFICIAL COLORING NO GLUTEN - NO MSG - NO SOY NO... recall (Organic Spices, Inc)
  FoodClass IIReported February 11, 2026 · Product contains salt and is mislabeled
• spicely ORGANIC garlic salt NO ARTIFICIAL COLORING NO GLUTEN - NO MSG - NO SOY NO... recall (Organic Spices, Inc)
  FoodClass IIReported February 11, 2026 · Product contains salt and is mislabeled
• Repackaged M&Ms candies recall (Beacon Promotions Inc)
  FoodClass IIReported February 11, 2026 · Undeclared allergens (milk, soy, and peanut)
• Repackaged M&Ms Peanut candies recall (Beacon Promotions Inc)
  FoodClass IIReported February 11, 2026 · Undeclared allergens (milk, soy, and peanut)
• Organic Chia Seed Black Origin: PARAGUAY Net weight: 55.12 LBS Produced for: Tradin... recall (Tradin Organics USA LLC)
  FoodClass IReported February 11, 2026 · Potential contamination with Salmonella.
• WinCo Foods Deli Margherita Pizza Thin Crust recall (WinCo Foods LLC)
  FoodClass IIReported February 11, 2026 · Product may contain foreign material (metal fragments).
• GLUTEN FREE 14" SEASONED VEGAN PIZZA CRUST recall (Rich Products Corp)
  FoodClass IIReported February 11, 2026 · Product contains undeclared milk and egg
• Diclofenac Sodium recall (SUN PHARMACEUTICAL INDUSTRIES INC)
  DrugClass IIReported February 11, 2026 · Failed Viscosity Specifications: Out of Specification (OOS) [slightly lower than the limit] result in viscosity for Diclofenac Sodium Gel, 3%.
• Trazodone Hydrochloride recall (Granules Pharmaceuticals Inc.)
  DrugClass IIReported February 11, 2026 · Presence of Foreign Tablets/Capsules
• Bisoprolol Fumarate and Hydrochlorothiazide tablets recall (Unichem Pharmaceuticals USA Inc.)
  DrugClass IIReported February 11, 2026 · cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.
• Bubble Sensor for 3/8" x 3/32" tubing recall (Maquet Cardiopulmonary Gmbh)
  Medical deviceClass IIReported February 11, 2026 · Internal investigations have identified an issue with the durability of the connecting cable near the connection to the Venous Bubble Sensor. Excessive bending...
• FDR Visionary Suite recall (FUJIFILM Healthcare Americas Corporation)
  Medical deviceClass IIReported February 11, 2026 · It was found that the contacts of the electromagnetic contactors used inside the cabinet of the X-ray high-voltage generator were welded, and the current might...
• Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3025... recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3020... recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Brand Name: Disposable Triple Lumen Sphincterotome Product Name: Disposable Triple... recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3030... recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1530... recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520... recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V431M-0730 recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V431M-0720 recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0730 recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0725 recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0720 recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0330 recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:... recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Product Name: Single Use Sphincterotome V recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.
• Brand Name: CleverCut Product Name: Single Use 3-Lumen Sphincterotome V ... recall (Olympus Corporation of the Americas)
  Medical deviceClass IIReported February 11, 2026 · Devices which did not undergo thermoforming could deform and lose performance.

← NewerOlder →