replacement available Recalls

1,215 recalls tagged with “replacement available”.

Food & Beverages
HIGH
FDA FOOD

Made Fresh Salads Garlic & Herb Cream Cheese 5 lb Tub Recalled for Listeria Contamination (2026)

Made Fresh Salads Inc recalled 557 five-pound tubs of Garlic & Herb Cream Cheese sold in New York after a confirmed Listeria monocytogenes contamination. The recall was activated on February 19, 2026 and remains active as of March 18, 2026. Consumers who purchased the product should not consume it and should contact the company for refund or replacement guidance.

Made Fresh Salads
Products may
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Food & Beverages
HIGH
FDA FOOD

Sunflour Bakery Recalls 1 Bag Hamburger Bun Over Undeclared Sesame Seed (2026)

Sunflour Bakery recalled 1 bag of Hamburger Bun, 18oz with six buns sold to a single Orange County retailer. The recall involves sesame seeds not declared on the label. Consumers should not eat the product and should contact Sunflour Bakery by email for refund or replacement.

NRS Enterprises, Inc. dba Sunflour Bakery
Undeclared sesame
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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 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 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 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 DEVICE

XTANT Medical Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm Recalled for Mislabeling of Screw S

XTANT Medical Holdings recalls 2 units of the Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm due to mislabeled lot that misidentifies screw length. The recall affects units distributed in the US, specifically Oregon. Healthcare providers and patients should stop using the device immediately and follow manufacturer instructions for recall actions.

XTANT Medical Holdings
Units from
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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

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 DEVICE

Molded Products MPC-130 See Luer Cap Set Recalled for High-Risk Assembly Issue (2026)

Molded Products recalled 26,900 MPC-130 See Luer Cap Sets used in intravascular administration nationwide in the United States. The recall is active as of 2026-04-15. The threaded sleeve may not engage and can detach. Health risk is high. Stop using the device and follow the manufacturer’s recall instructions.

Molded Products
Molded Products,
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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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Tag Statistics

Total Recalls
1,215

Related Tags

chemical hazardpoisoning riskinfant productlaceration riskchoking hazardfire hazardburn riskelectrical hazardstop use immediatelyreturn for refundfda regulatedcpsc regulated
    replacement available Recalls | RecallRadar