Safety Recalls

17,559 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 3,551–3,600 of 17,559

• Drug Recall · February 13, 2026

  Harbin Jixianglong Biotech Co., Ltd.

  Semaglutide, For Rx compounding use only, packaged in a) 1g, NDC 84385-106-01; b) 5g, NDC 84385-106-02; c) 10g, NDC 84385-106-06; d) 25g, NDC 84385-106-03; d) 50g, NDC 84385-106-04 Manufacturer: Harbi

  CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution

  Class II

• Medical Device Recall · February 13, 2026

  Medtronic MiniMed, Inc.

  MiniMed 530G Insulin Pump (MMT-551, MMT-751)

  All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.

  Class II

• Medical Device Recall · February 13, 2026

  Medtronic MiniMed, Inc.

  Paradigm REAL-Time Insulin Pump (MMT-522, MMT-722)

  All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.

  Class II

• Medical Device Recall · February 13, 2026

  Medtronic MiniMed, Inc.

  MiniMed 620G Insulin Pump (MMT-1750)

  All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.

  Class II

• Medical Device Recall · February 13, 2026

  Merit Medical Systems, Inc.

  CentrosFLO Hemodialysis Catheters, REF: CENFP15K/A, CENFP15K/B, CENFP17K/A, CENFP19K/A, CENFP23K/A, CENFP27K/A, CENFP31K/A, CENFT15K, CENFT15K/D, CENFT17K, CENFT17K/A, CENFT17K/D, CENFT19K, CENFT19K/A

  16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure delay, embolization/thrombosis, impaired catheter function, loss of vessel for future vascular access.

  Class I

• Medical Device Recall · February 13, 2026

  Medtronic MiniMed, Inc.

  Paradigm Insulin Pump (MMT-712, MMT-715)

  All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.

  Class II

• Medical Device Recall · February 13, 2026

  Merit Medical Systems, Inc.

  ProGuide Chronic Dialysis Catheters, REF: DC01455550/C, DC21452419/C, DC21452419-NE5/C, DC21452823-NE5/C, DC21454035/C, DC21455550/C

  16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure delay, embolization/thrombosis, impaired catheter function, loss of vessel for future vascular access.

  Class I

• Food Recall · February 13, 2026

  Shaman Botanicals, LLC

  Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 225mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.25 oz 30 TABLETS Sup

  A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.

  Class I

• Food Recall · February 13, 2026

  Shaman Botanicals, LLC

  Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 15mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.02 oz 2 TABLETS Suppl

  A sample of the product had the active ingredient in a quantity greater than the labeled specification.

  Class I

• Food Recall · February 13, 2026

  Ambrosia Brands LLC

  Rosabella brand MORINGA; DIETARY SUPPLEMENT CAPSULES; 60 capsules per bottle; Distributed by: Ambrosia Brands, LLC, 625 Randall Ave, St. 100, Cheyenne, WY 82001; SUGGESTED USE: As a dietary supplement

  Product may be contaminated with Salmonella

  Class I

• Consumer Product Recall · February 12, 2026

  Leioujiapin Technology Co., Ltd. dba Beloems, of China

  Beloems Adult Portable Bed Rails

  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 rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. The bed rails do not meet structural stability or retention strap requirements, posing a fall hazard. The bed rails' push pins and push pin holes are incorrectly sized, posing a laceration hazard.

  Unclassified

• Consumer Product Recall · February 12, 2026

  Guangzhou Kezhinuo Maoyi Youxian Gongsi, dba Fortemotus Direct US, of China

  Fortemotus Adult Portable Bed Rails

  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 rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. The bed rails do not meet structural stability or retention strap requirements, posing a fall hazard. The bed rails' push pins and push pin holes are incorrectly sized, posing a laceration hazard.

  Unclassified

• Consumer Product Recall · February 12, 2026

  Shenzhen Zhongyuantong Technology Co., Ltd., dba SOOWERY of China

  SOOWERY 6-Drawer Dressers

  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 death to children. The dressers violate the mandatory standard as required by the STURDY Act.

  Unclassified

• Consumer Product Recall · February 12, 2026

  Surveying Accessories Cheaper, of Miami, Florida

  Colombia-themed Magnetic Board Games

  The recalled board games violate the mandatory standard for toys because the magnetic game pieces contain loose high-powered magnets, posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

  Unclassified

• Medical Device Recall · February 12, 2026

  Olympus Corporation of the Americas

  Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444.

  The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

  Class II

• Medical Device Recall · February 12, 2026

  Erbe USA Inc

  Flexible Cryoprobe (OD 1.1mm, L1.15mm) w/ oversheath (OD2.6mm, L817mm) REF: 20402-401 STERILE EO. For surgical use

  Probes may rupture/burst during activation

  Class I

• Consumer Product Recall · February 12, 2026

  Hangzhouyoupengmaoyiyouxiangongsi (Hangzhou Youpeng Trading Co., Ltd.), dba Babibaby, of China

  CheerKid Baby Bath Seats

  The recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.

  Unclassified

• Vehicle Recall · February 12, 2026

  Nissan North America, Inc.

  2024 NISSAN ROGUE, 2025 NISSAN ROGUE

  Broken throttle body gears can cause a loss of drive power, increasing the risk of a crash.

  Unclassified

• Vehicle Recall · February 12, 2026

  International Motors, LLC

  2026 INTERNATIONAL MV

  A vehicle that does not automatically brake as expected increases the risk of a crash.

  Unclassified

• Vehicle Recall · February 12, 2026

  Nissan North America, Inc.

  2023 NISSAN ROGUE, 2024 NISSAN ROGUE, 2025 NISSAN ROGUE

  Engine failure can cause a loss of drive power, increasing the risk of a crash. A bearing failure may cause a breach in the engine block, allowing hot oil to be discharged, increasing the risk of an engine fire.

  Unclassified

• Medical Device Recall · February 12, 2026

  Erbe USA Inc

  Flexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use

  Probes may rupture/burst during activation

  Class I

• Vehicle Recall · February 12, 2026

  General Motors, LLC

  2024 CADILLAC LYRIQ

  An inoperative rearview camera can reduce the driver's rear visibility, increasing the risk of a crash.

  Unclassified

• Medical Device Recall · February 12, 2026

  Olympus Corporation of the Americas

  Olympus Endoscope Reprocessor OER-Elite. Model Number: N5789340.

  The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

  Class II

• Medical Device Recall · February 12, 2026

  Olympus Corporation of the Americas

  Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443.

  The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

  Class II

• Drug Recall · February 12, 2026

  Slate Run Pharmaceuticals

  Eptifibatide Injection, 75 mg/100 mL vial for weight-adjusted bolus dosing, 1x100 mL Single-dose Vial, For Intravenous Use Only, Rx Only, Manufactured by: Hainan Poly Pharm. Co., Ltd., Guilinyang Econ

  Labeling: Not Elsewhere Classified. The carton for Eptifibatide Injection 75 mg/100 mL states 75 mg/100 mL vial for weight-adjusted bolus dosing. The approved statement is 75 mg/100 mL vial for weight-adjusted infusion.

  Class III

• Consumer Product Recall · February 12, 2026

  Jet Importer: Watkins Manufacturing Corporation, of Vista, California

  Hydromassage Rotary Jet (6 fin) in Highlife Collection spas

  The hydromassage rotary jets can create a suction force that allows the user's hair to be entangled, submerging their head underwater, posing entanglement and drowning hazards to the user.

  Unclassified

• Consumer Product Recall · February 12, 2026

  TIANJINSHIHAOWEIXINSHENGJIDIANANZHUANGGONGCHENG, of China

  3-Pack Smoke Detector Fire Alarms

  If the sensing threshold of security warnings is set too high, the alarm might not sound in a timely manner, posing a fire hazard.

  Unclassified

• Medical Device Recall · February 12, 2026

  Erbe USA Inc

  Flexible Cryoprobe (OD 2.4mm, L1.15mm) REF: 20402-411. For surgical use

  Probes may rupture/burst during activation

  Class I

• Food Recall · February 12, 2026

  SUNGAL INC

  XZL, Jelly Snacks, 12.68 OZ, Bag. 12 Bags per Case.

  Product Contains undeclared FD&C Yellow #5 & #6 and Red #40

  Class II

• Food Recall · February 12, 2026

  Oregon Potato Company LLC

  IQF frozen Blueberry (30lbs. cases and 1400 lbs. totes), product of USA. Product is packaged in polyethylene bag within a corrugated 30lbs. case or packaged in polyethylene liner within a Gaylord 14

  Listeria monocytogenes

  Class I

• Medical Device Recall · February 12, 2026

  Olympus Corporation of the Americas

  Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140.

  The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

  Class II

• Medical Device Recall · February 11, 2026

  Burlington Medical, LLC

  Burlington Medical, Wrap Aprons.

  Potential for attenuation degradation over time, decreasing the lifespan.

  Class II

• Medical Device Recall · February 11, 2026

  Waldemar Link GmbH & Co. KG (Mfg Site)

  Embrace Drill Tower, Standard/Lateral (25mm); Item Number: 645-081/63;

  The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the individual surgical steps described in the surgical technique are correct.

  Class II

• Vehicle Recall · February 11, 2026

  Daimler Trucks North America, LLC

  2023 WESTERN STAR 47X, 2025 WESTERN STAR 47X, 2027 WESTERN STAR 49X

  A short circuit increases the risk of a fire.

  Unclassified

• Medical Device Recall · February 11, 2026

  Burlington Medical, LLC

  Burlington Medical, Kilt Blockers.

  Potential for attenuation degradation over time, decreasing the lifespan.

  Class II

• Medical Device Recall · February 11, 2026

  Waldemar Link GmbH & Co. KG (Mfg Site)

  Embrace Drill Tower, Wedged (25mm); Item Number: 645-081/62;

  The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the individual surgical steps described in the surgical technique are correct.

  Class II

• Medical Device Recall · February 11, 2026

  Burlington Medical, LLC

  Burlington Medical, Protective Sleeves.

  Potential for attenuation degradation over time, decreasing the lifespan.

  Class II

• Medical Device Recall · February 11, 2026

  Burlington Medical, LLC

  Burlington Medical, Vest

  Potential for attenuation degradation over time, decreasing the lifespan.

  Class II

• Medical Device Recall · February 11, 2026

  TMJ Solutions Inc

  TMJ Bilateral Implants, REF: CHG020

  Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided open bite.

  Class II

• Medical Device Recall · February 11, 2026

  Burlington Medical, LLC

  Burlington Medical, Blockers.

  Potential for attenuation degradation over time, decreasing the lifespan.

  Class II

• Medical Device Recall · February 11, 2026

  Burlington Medical, LLC

  Burlington Medical, Thyroid Shield.

  Potential for attenuation degradation over time, decreasing the lifespan.

  Class II

• Medical Device Recall · February 11, 2026

  CareFusion 303, Inc.

  BD Alaris" System with Guardrails" Suite MX with Point of Care Unit

  Due to product labeling not indicating which Transport Layer Security (TLS) version that must be enabled on hospital network to ensure secure Wi-Fi communication with Point-of-Care Units

  Class II

• Medical Device Recall · February 11, 2026

  Burlington Medical, LLC

  Burlington Medical, Caps.

  Potential for attenuation degradation over time, decreasing the lifespan.

  Class II

• Medical Device Recall · February 11, 2026

  Burlington Medical, LLC

  Burlington Medical, Kilt

  Potential for attenuation degradation over time, decreasing the lifespan.

  Class II

• Vehicle Recall · February 11, 2026

  Triumph Motorcycles America, Ltd.

  2023 TRIUMPH BONNEVILLE T120

  Overheated wiring increases the risk of a crash or fire.

  Unclassified

• Food Recall · February 11, 2026

  Juniper Granola, LLC

  Junebar Chocolate Cherry All Natural Snack Bar; INGREDIENTS: ORGANIC ALMOND BUTTER, DATE PASTE, ORGANIC BLACK BEANS, ORGANIC SWEET POTATOES, GLUTEN FREE ROLLED OATS, SEMI-SWEET SOY FREE VEGAN CHOCOLAT

  Products contain undeclared milk and soy.

  Class I

• Medical Device Recall · February 11, 2026

  Burlington Medical, LLC

  Burlington Medical, BAT (Breast, Axilla and Thyroid) Coverage.

  Potential for attenuation degradation over time, decreasing the lifespan.

  Class II

• Medical Device Recall · February 11, 2026

  Burlington Medical, LLC

  Burlington Medical, Demi Half Aprons.

  Potential for attenuation degradation over time, decreasing the lifespan.

  Class II

• Medical Device Recall · February 11, 2026

  Burlington Medical, LLC

  Burlington Medical, Leg Wraps.

  Potential for attenuation degradation over time, decreasing the lifespan.

  Class II

• Medical Device Recall · February 11, 2026

  Burlington Medical, LLC

  Burlington Medical, Frontal Aprons

  Potential for attenuation degradation over time, decreasing the lifespan.

  Class II