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This category has a significant number of recalls. Check it regularly if you own products in this area.
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.
The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.
Thrasio recalled Angry Orange Enzyme Stain Removers on January 22, 2026. The products may contain the bacteria Pseudomonas aeruginosa, posing serious health risks. Consumers should stop using the product and seek a refund immediately.
cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.
Due to pediatric defibrillator electrode delamination
Stryker recalled 5,864 units of the MOLLI 2 surgical markers on January 21, 2026. The recall follows concerns that magnetic surgical tools may dislodge markers during procedures. Healthcare providers and patients must stop using these devices immediately.
Unichem Pharmaceuticals recalled 60,000 bottles of Doxazosin Tablets on January 21, 2026. The tablets were imprinted with the wrong ID, posing a serious risk to consumers. Healthcare providers and users should stop using the product immediately.
Nationwide recall of Dukal BZK Antiseptic Towelettes due to CGMP deviations. The products are manufactured for Dukal, LLC in Ronkonkoma, NY and distributed across the United States. Stop using immediately and contact ACME United Corporation for guidance.
ACME United Corporation recalled 212,607,900 First Aid Only BZK Antiseptic Towelettes sold nationwide. The recall cites CGMP deviations in manufacturing. Consumers should stop using the product immediately and contact ACME United Corporation for guidance.