2,715 recalls tagged with “immediate action”.
Asteria Health recalled 7,840 testosterone pellets on January 26, 2026, due to potential metal particulate matter contamination. Consumers must stop using the product immediately and contact healthcare providers for guidance. The recall affects products distributed nationwide in the USA.
Asteria Health recalled 1,758 testosterone pellets on January 26, 2026, due to potential metal particulate contamination. The recall affects pellets distributed nationwide in the USA. Consumers should stop using the product immediately and contact their healthcare providers for guidance.
Asteria Health recalled 3,871 testosterone pellets on January 26, 2026, due to potential metal particulate matter. The recall affects products distributed nationwide in the USA. Consumers should stop using the product immediately and seek guidance from their healthcare providers.
Asteria Health recalled 100 sterile pellets of testosterone and anastrozole on January 26, 2026. The recall stems from potential metal particulate contamination. Consumers must stop using the product immediately and consult healthcare providers for guidance.
Asteria Health recalled 70,959 testosterone pellets on January 26, 2026, due to potential metal contamination. Consumers must stop using the product immediately. The recall affects multiple lots distributed nationwide in the USA.
Asteria Health recalled 670 testosterone pellets on January 26, 2026, due to potential metal particulate contamination. Consumers and healthcare providers must stop using the product immediately. The recall affects all units distributed nationwide in the United States.
Philips Medical Systems recalled 5,136 Azurion 7 M20 systems on January 26, 2026. The devices may move unexpectedly when the Reset Geometry button is pressed, posing a danger to patients and healthcare providers. Consumers should stop using the devices immediately and contact the manufacturer for instructions.
Philips Medical Systems Nederland B.V. recalled 802 Azurion 3 M15 systems on January 26, 2026. The systems may move unexpectedly, posing a risk to patients and healthcare providers. Consumers should stop using the device immediately and follow recall instructions.
Gerber Products Company recalled 258,474 cases of its Arrowroot Biscuits on January 26, 2026. The recall follows potential contamination of the product with pieces of soft kraft paper or plastic. Consumers should not consume the biscuits and seek refunds immediately.
Mangalm LLC recalled Tops GOLD Mixed Pickle sold in California, Nevada, Oregon, Utah and Washington after FDA enforcement. The product may be adulterated with erucic acid from mustard oil. Consumers who purchased it should not eat it and should contact Mangalm for refund or replacement via email.
Mangalm LLC recalled 40 cases of Tops GOLD Stuffed Red Chilli Pickle, 31.74 oz cans, distributed in California, Nevada, Oregon, Utah and Washington. The recall is due to potential adulteration with erucic acid from mustard oil. Consumers should not consume this product and should contact Mangalm LLC by email for a refund or replacement.
Mangalm LLC recalls Tops GOLD Green Chilli Pickle, 31.74 oz cans sold in California, Nevada, Oregon, Utah and Washington. The recall cites potential adulteration with erucic acid from mustard oil ingredients. Consumers who purchased this product should not consume it and should contact Mangalm LLC for refund or replacement by email.
Mangalm LLC recalls 40 cases of Tops GOLD Lime Pickle, 31.74 oz jars, produced in India and distributed to California, Nevada, Oregon, Utah and Washington. The recall follows potential adulteration with erucic acid from mustard oil. Consumers who have purchased the product should not consume it and should contact Mangalm LLC for a refund or replacement via email.
Mangalm recalls Tops GOLD Mango Pickle after FDA enforcement flagged potential erucic acid adulteration. The recall covers two UPCs and two can sizes distributed in five Western states. Consumers are urged not to eat the product and to contact Mangalm for refunds or replacements.
Mangalm LLC recalled Tops GOLD Khatta Meetha Pickle after confirming potential erucic acid adulteration from mustard oil. The recall covers 40 cases distributed in CA, NV, OR, UT and WA. Consumers should not consume the product and should contact Mangalm LLC for refund or replacement information via email.
I.T.S. GmbH has recalled 5,568 units of the I.T.S. Screw System sold nationwide in the United States after MRI safety tests showed higher RF-induced temperature increases under some MRI conditions than the IFU outlined. The defect involves MRI RF heating that could burn patients. Patients and healthcare providers should stop using the device immediately and follow the recall instructions.
ITS GmbH recalled 510 units of the I.T.S Straight Plate with Angular Stability after MRI safety testing showed higher RF-induced temperature increases under certain MRI conditions. The recall covers multiple article numbers across forearm and straight plates and distributions nationwide in the United States. No injuries or incidents have been reported at this time. Healthcare providers andpatients
ITS GmbH recalled 176 units nationwide in the United States after MRI safety testing showed higher RF-induced temperature increases under certain MRI conditions. The issue could cause burns during MRI exposure. Healthcare providers and patients should stop using the device immediately and follow recall instructions.
I.T.S. GmbH recalled 220 Volar Radius Plate PROlock II devices after updated MRI safety testing showed higher RF-induced temperatures under certain MRI conditions. The devices were distributed nationwide in the United States. Clinicians and patients should stop using the device immediately and follow the manufacturer recall instructions.
ITS GmbH recalled 11 Pelvic Reconstruction System PRS components after MRI safety testing showed higher RF-induced temperature increases under certain MRI conditions than described in the IFU. The recall covers Fixation Screw 70312 and Spike short 70314. Healthcare providers and patients should stop using the devices and follow the manufacturer’s recall instructions provided by email.