All Product Recalls

Browse through 2,970 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Health & Personal Care
HIGH
FDA DRUG

Major Pharmaceuticals Chlorpromazine Hydrochloride 200 mg Recall Involves 1,394 Blister Packs (2025)

Major Pharmaceuticals recalled 1,394 blister packs of Chlorpromazine Hydrochloride Tablets, 200 mg, distributed nationwide. The recall cites CGMP deviations with the presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit. Healthcare providers and patients are urged to stop using the product and await guidance from Major Pharmaceuticals and Rugby Laboratories.

Chlorpromazine Hydrochloride
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

GE HealthCare Recalls SMV DSXi Nuclear Medicine Gamma Camera (205 Units) for Cardiac Imaging

GE HealthCare recalled 205 SMV DSXi dual-head nuclear medicine gamma cameras used for cardiac imaging distributed worldwide. The recall cites potential detector mounting stress after End of Guaranteed Service. Hospitals should stop using these devices and follow the manufacturer’s recall instructions. Contact GE Medical Systems Israel Functional Imaging or a healthcare provider for guidance.

GE HealthCare
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

Noah Medical Galaxy System GAL-001 Recall of 47 Units for Password-Protected Manual Access (2025)

Noah Medical recalled 47 Galaxy System bronchoscopic visualization devices distributed to 20 US states and internationally to Hong Kong and Australia. The recall centers on password-protected Instructions for Use. Healthcare providers and patients should stop using the device immediately and follow manufacturer recall instructions.

Noah Medical
Due to
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Health & Personal Care
HIGH
FDA DRUG

Major Pharmaceuticals Chlorpromazine Hydrochloride 50 mg Tablets Recalled for Nitrosamine Impurity (

Major Pharmaceuticals, via The Harvard Drug Group LLC, recalled 506 blister packs of Chlorpromazine Hydrochloride tablets, 50 mg, distributed nationwide. A CGMP deviation shows the presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit. Stop using the product and contact the Harvard Drug Group or Rugby Laboratories for guidance.

Major Pharmaceuticals
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Major Pharmaceuticals Chlorpromazine 25 mg Tablets Recalled for Nitrosamine Contamination (1256 Bls,

Major Pharmaceuticals recalled 1,256 blister packs of Chlorpromazine Hydrochloride tablets, 25 mg, sold nationwide in the United States. A CGMP deviation led to the presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake. Healthcare providers and patients should stop using the product and contact Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories for next-步

Chlorpromazine Hydrochloride
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

UIH Technologies uCT 780 MD CT Scanner Recalled for Cover Interference (2025)

UIH Technologies recalled 2 units of the uCT 780 MD computed tomography system after an FDA enforcement notice Z-0220-2026. A third-party outer cover can become trapped between the patient table and gantry, causing mechanical interference during table movement. Hospitals should stop using the device immediately and await instructions from UIH Technologies LLC or their healthcare provider.

UIH Technologies
Third-party outer
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Health & Personal Care
HIGH
FDA DEVICE

UIH Technologies Recalls 11 uCT 760 MD CT Scanners for Cover Interference Risk (2025)

UIH Technologies recalled 11 units of the uCT 760 MD Computed Tomography X-ray System. Third-party outer covers can become trapped between the patient table and gantry, causing mechanical interference during table movement. Hospitals and patients should stop using the device immediately and await manufacturer instructions.

UIH Technologies
Third-party outer
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems Israel Recalls 11 Elscint Cardial Gamma Cameras in 2025

GE Medical Systems Israel recalls 11 Elscint Cardial dual-head gamma cameras used for cardiac imaging worldwide. The recall concerns detector mounting that could fail if the unit is moved without proper support. Hospitals should stop using these devices immediately and follow GE’s recall instructions.

GE Medical Systems Israel
GE HealthCare
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Food & Beverages
HIGH
FDA FOOD

E&E Foods Goldband Snapper Fillets Recalled for Species Mislabeling (925 Cases) 2025

E&E Foods recalled 925 cases of Goldband Snapper Fillets sold in CO, IL, MO, MN and UT after FDA testing found the product is Sharptooth Snapper. The fish is wild caught in Indonesia and distributed by E&E Foods. Consumers who bought this product should not consume it and should contact E&E Foods for refund or replacement information.

E&E Foods
Goldband Snapper
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Recalled Bottle of Bariatric Fusion High ADEK Multivitamin
HIGH
CPSC

Blueroot Health Recalls Bariatric Fusion Iron Multivitamins Over Child Poisoning Risk (2025)

Blueroot Health recalled Bariatric Fusion iron multivitamin bottles after discovering the packaging is not child-resistant. The recall involves two bottle types with 45 mg of iron. Affected bottles lack the required push-down-and-turn caps and carry specific lot numbers. Consumers should stop using the product and contact Blueroot Health for a free child-resistant replacement cap.

Blueroot Health
The recalled
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Recalled In My Jammers Button Up Flare Set – Victoria print
HIGH
CPSC

In My Jammers Recalls Button Flare Pajama Sets for Burn Hazard in 2025

In My Jammers recalls children's button-up flare pajama sets sold online after the company violated mandatory flammability standards. The recall, active as of Sept. 11, 2025, involves sets in multiple prints and sizes. Parents should stop using them and seek a full refund or store credit.

In My Jammers
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Olympus BF-H1100 Bronchovideoscope Recall 1,867 Units Overseas in 2025

Olympus BF-H1100 bronchovideoscopes sold nationwide in the US were recalled. The recall updates the IFU to clarify safe use with laser, argon plasma coagulation, and high-frequency therapy equipment. Stop using the device immediately and follow the manufacturer’s recall instructions.

Olympus
Additional IFU
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific Recall: Preconnect with TENACIO Pump with InhibiZone Affects 172 Units Worldwide

Boston Scientific recalled 172 units of the CXR Preconnect with TENACIO Pump with InhibiZone worldwide. The recall was initiated on 2025-09-11 and remains active as of 2025-10-22. The devices can experience inflation and/or deflation performance issues. Healthcare providers should stop using the devices and follow manufacturer instructions for recall remediation.

Boston Scientific
The potential
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Health & Personal Care
HIGH
FDA DEVICE

Insulet Omnipod 5 iOS App Recall Affects 174,013 Units in 2025

Insulet recalled 174,013 Omnipod 5 iOS app software units distributed nationwide in the United States. The recall cites a magnifying feature bug that can duplicate a single-digit entry. This could lead to bolus insulin dosing errors and hypoglycemia. Stop using the app immediately and follow recall instructions from Insulet or your healthcare provider.

Insulet
The failure
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Health & Personal Care
HIGH
FDA DEVICE

OLYMPUS BF-1T150 Bronchoscope Recall in 2025 for Updated IFU on Safe Use

Olympus Corporation of the Americas recalled 1,990 BF-1T150 bronchoscopes distributed nationwide to healthcare providers. The recall updates the IFU to clarify safe use with laser, argon plasma coagulation and high-frequency therapy equipment. Healthcare facilities should stop using the devices immediately and follow the manufacturer’s recall instructions.

Olympus Corporation of the Americas
Additional IFU
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific TENACIO Pump Recall 2025 for Inflation Deflation Issues

Boston Scientific recalled the TENACIO Pump without InhibiZone (UPN 72404420) worldwide, including the US and Canada. The device may experience inflation and/or deflation performance issues. Patients and healthcare providers should stop using the device immediately and follow the manufacturer's recall instructions.

Boston Scientific
The potential
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Health & Personal Care
HIGH
FDA DEVICE

Olympus BF-1TQ170 Bronchoscope Recall Expanded for IFU Clarifications

Olympus Corporation of the Americas recalls the BRONCHOVIDEOSCOPE BF-1TQ170. The recall is active with 2,092 units in the outside US market and no US units affected. The action seeks updated instructions for safe use with laser and high-frequency therapy equipment. Healthcare providers should stop use and follow manufacturer recall instructions.

Olympus Corporation of the Americas
Additional IFU
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Health & Personal Care
HIGH
FDA DEVICE

Olympus BF-1T60 Bronchofiberscope Recall for IFU Updates (2025)

Olympus recalled 3,216 BF-1T60 bronchofiberscopes distributed nationwide and internationally after updating instructions for safe use with laser, argon plasma coagulation and high-frequency therapy equipment. The recall updates guidance to reduce risk during advanced energy-device procedures. Clinicians and facilities should stop using the devices and follow manufacturer instructions for recall.

Olympus Corporation of the Americas
Additional IFU
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