All Product Recalls

Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Health & Personal Care
HIGH
FDA DEVICE

Baxter Recalls 19 Blue Volara Ventilator Adapters for Home Use (2026)

Baxter Healthcare recalled 19 Blue Ventilator Adapter Modules used with the Volara Respiratory Therapy system in Florida after an urgent correction flagged potential oxygen desaturation and barotrauma risks in home care. The correction provides home caregiver instructions for use. Patients and healthcare providers should stop using this device immediately and contact Baxter or a healthcare provide

Baxter
Urgent Medical
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Health & Personal Care
HIGH
FDA DEVICE

Mentor Texas CPX 4 US Breast Tissue Expanders Recall 2026

Mentor Texas, LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs worldwide on February 18, 2026. The recall covers models SCPX-107MH, SCPX-117MH, SCPX-127MH, SCPX-135MH, SCPX-146MH and SCPX-156MH. Infusion sets may include a dull needle tip that is difficult to advance and may break. Stop using the device and follow recall instructions from the manufacturer, with recall notification by-

Mentor Texas
Infusion sets
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Health & Personal Care
HIGH
FDA DEVICE

Mentor CPX 4 Breast Tissue Expanders Recalled in 2026 for Dull Needle Tip Hazard

Mentor Texas LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs on February 18, 2026. Infusion sets may have dull or blunt needle tips that can be difficult to advance or break. Health facilities and patients should stop using the device immediately and follow the recall instructions.

Mentor Texas LP
Infusion sets
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Health & Personal Care
HIGH
FDA DEVICE

Mentor Texas LP Recalls CPX 4 US Breast Tissue Expanders with Suture Tabs (2026)

Mentor Texas LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs sold worldwide, including US nationwide, after determining infusion sets may contain a dull needle tip. The defect may hinder needle advancement or cause breakage during use. Patients and providers should stop using the device immediately and follow recall instructions from the manufacturer.

Mentor Texas
Infusion sets
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Health & Personal Care
HIGH
FDA DEVICE

Mentor Texas Artoura Breast Tissue Expanders Recalled Worldwide in 2026

Mentor Texas, LP recalled Artoura Breast Tissue Expanders sold worldwide, including the United States. The infusion sets may contain a dull or blunt needle tip, which may be difficult to advance or break. Healthcare providers and patients should stop using the affected devices and await recall instructions by letter.

Mentor Texas
Infusion sets
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Health & Personal Care
HIGH
FDA DEVICE

Medline Sterile Radiology Procedure Kits Recalled for Sterility Breach (2026)

Medline Industries recalled 420 Sterile Radiology Procedure Kits, Model DYNDH1491B, distributed nationwide in Minnesota after a potential breach in sterile pouch packaging. The defect may compromise product sterility. Stop using the kit immediately and contact Medline or your healthcare provider for instructions.

Medline Industries, LP
There is
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Health & Personal Care
HIGH
FDA DEVICE

Abiomed Purge Cassette Recall 2026: 33,107 Impella Pump Sets Worldwide Over Purge Leaks

Abiomed has issued a Class I recall for 33,107 Purge Cassette units used with Impella pump sets worldwide due to purge leaks in Generation 1 cassettes. The leaks raise the risk of compromised device performance. Patients and healthcare providers should stop using the affected devices immediately and follow Abiomed's recall instructions.

Abiomed
Increased risk
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Health & Personal Care
HIGH
FDA DEVICE

Mentor Artoura Breast Tissue Expanders Recall for Dull Needle Tips (2026)

Mentor Texas, LP is recalling Artoura Breast Tissue Expanders with infusion sets worldwide, including the United States and Canada. The infusion sets may contain dull or blunt needle tips that are difficult to advance or may break. Patients and healthcare providers should stop using the device and follow recall instructions.

Mentor
Infusion sets
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Health & Personal Care
HIGH
FDA DEVICE

Mentor Texas CPX 4 Breast Tissue Expander Recall 2026 for Dull Needle Tips

Mentor Texas, LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs sold worldwide, including the US. Infusion sets may have a dull or blunt needle tip that is difficult to advance or may break. Patients and healthcare providers should stop using the device immediately and contact Mentor Texas, LP for instructions.

Mentor Texas
Infusion sets
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Health & Personal Care
HIGH
FDA DRUG

Kirkman MAXIMUM Zone 1 4% Lidocaine Cream Recall 178 Bottles (2026)

Kirkman recalled 178 bottles of MAXIMUM Zone 1 4% Lidocaine Cream distributed nationwide in the U.S. by Dermal Source. The recall cites stability data that does not support the stated expiry date. Consumers and healthcare providers should stop using this product immediately and contact Kirkman for guidance.

Kirkman
Stability Data
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Health & Personal Care
HIGH
FDA DRUG

Kirkman MAXIMUM ZONE 2 4% Lidocaine Cream Recall for Expiry Stability Issue (2026)

HTO Nevada Inc. dba Kirkman recalled 243 bottles of MAXIMUM ZONE 2, 4% lidocaine cream distributed nationwide by Dermal Source. The recall cites stability data that does not support an expiry date. Consumers and healthcare providers should stop using this product immediately and contact Kirkman for guidance.

HTO Nevada Inc. dba Kirkman
Stability Data
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Health & Personal Care
HIGH
FDA DRUG

Nilotinib Capsules 200 mg Recall: 164 Cartons Nationwide in 2026

Nilotinib capsules manufactured for Cipla USA are recalled nationwide after stability testing showed out-of-spec results. The failure involves description and appearance by visual inspection at six months of long-term stability. Patients and healthcare providers should stop using the product immediately and contact Cipla USA for guidance.

Nilotinib
Failed Tablet/Capsule
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Health & Personal Care
HIGH
FDA DRUG

Midodrine Hydrochloride Tablets Recall 8,892 Cartons Nationwide (2026)

Midodrine Hydrochloride Tablets, 5 mg, 50 tablets in 5 x 10 blister packs, distributed nationwide by Major Pharmaceuticals, are recalled. The packaging defect involves inadequately sealed blister packaging. Healthcare providers and patients should stop using the product immediately and contact The Harvard Drug Group LLC for guidance.

Midodrine Hydrochloride
Defective container;
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Health & Personal Care
HIGH
FDA DEVICE

Medline Anterior Hip Pack Recall Affects 14,379 Kits With Olympus Biopsy Valves (2026)

Medline Industries, LP recalled 14,379 anterior hip pack kits distributed nationwide after Olympus biopsy valves showed rubber fragment detachment. The defect can release fragments into the patient’s airway, risking a foreign body in the tracheobronchial tree and prolonging procedures. Stop using the kit and follow recall instructions from Medline and your healthcare provider.

Medline
Kits contain
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Health & Personal Care
HIGH
FDA DEVICE

Abiomed Impella Automated Controller Recall 62 Units in 2026

Abiomed recalled 62 Automated Impella Controller units sold to hospitals internationally. The recall warns of a delayed Purge System Blocked alarm display when used with first generation Impella 5.5 pumps. Hospitals should stop using the device immediately and contact Abiomed for instructions.

Abiomed
Potential that
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls 14,379 Olympus Biopsy-Valve Kits in 2026

Medline Industries is recalling 14,379 kits nationwide that include Olympus biopsy valves. The recall follows reports of rubber fragments detaching from the valves during use. Healthcare providers and patients should stop using the affected kits and follow Medline’s recall instructions.

Medline Industries, LP
Kits contain
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