2,756 recalls tagged with “immediate action”.
Philips Medical Systems Nederland recalled 2,317 Allura Xper FD10 imaging systems worldwide, including 497 in the United States. The BIOS battery may deplete faster than expected, causing the startup process to halt with no user alerts. Hospitals should stop using the devices and await manufacturer instructions.
Philips Medical Systems Nederland B.V. recalls 8 medical tables worldwide due to BIOS battery depletion risk. The recall affects Allura Xper FD20/15 OR Tables with model number 722059. The BIOS battery may deplete faster than expected, causing the system not to start without warning. Hospitals and healthcare providers should stop using the device immediately and follow the recall instructions.
Philips Medical Systems Nederland B.V. recalls 5,067 Allura Xper FD20 imaging systems worldwide. The BIOS battery may deplete faster than planned, causing the system to fail to start. The issue affects 1,626 US and 3,441 international units. Customers should stop using affected devices and follow manufacturer instructions.
Inpeco recalled eight FlexLab FLX System Potassium Test System units sold in California and New York. The recall targets the Sample Integrity Module HIL function, which detects hemolysis, icterus and lipemia. The FDA has not evaluated this function for safety or effectiveness, risking erroneous results or delays. Labs should stop using the device immediately.
The FlexLab X System Potassium Test System was recalled by Inpeco S.A. on 2025-09-03 after the FDA identified an unvalidated hemolysis, icterus, and lipemia function in its Sample Integrity Module. The recall affects US distribution to California and New York. Stop using immediately and follow manufacturer instructions.
New Spirit Naturals recalled 37 units of Ultra Whey Protein Powder sold directly through its online store after undeclared milk allergen was detected. The recall is currently active with a high-hazard designation. Consumers who have purchased the product should not consume it and should contact the company for refunds or replacements.
New Spirit Naturals recalled 178 units of Super Muscle Support Powder sold online after undeclared milk allergen was detected. The recall centers on milk not listed on the label. Consumers should stop using the product and contact New Spirit Naturals for refund or replacement.
Philips Medical Systems Nederland recall 115 Allura Xper FD20/20 imaging systems worldwide after reports that the BIOS battery may deplete prematurely. The startup process may halt with no user alert. Hospitals and providers should stop using affected units and await manufacturer instructions.
Philips Medical Systems Nederland B.V. recalls 5 Allura Xper FD20/20 OR Tables (Model 722039) worldwide. The BIOS battery may deplete faster than designed, halting startup with no warning. Hospitals should stop using the affected devices and follow recall instructions from Philips.
Beckman Coulter recalled 2,146 units of the SYNCHRON Systems Phosphorus (PHOSm) Reagent due to calibration failures that may delay patient results. Specific reagent lots may not function properly before their expiration date. Healthcare providers and patients must stop using these reagents immediately and follow manufacturer instructions.
A high-risk recall of sulfamethoxazole and trimethoprim 800 mg/160 mg double-strength tablets is active nationwide in the United States. The Harvard Drug Group and distribution partners have halted use of a lot due to a foreign-substance finding in packaging material. No tablets tested positive for micro-organisms. Consumers should stop using the product and consult their healthcare providers.
Major Pharmaceuticals recalls sulfamethoxazole and trimethoprim 800 mg/160 mg double-strength tablets sold nationwide. A specific lot of packaging coil used in production was found to contain a microorganism in the packaging area, though no microorganism was detected on the tablets. Consumers should stop using the product and follow guidance from Major Pharmaceuticals or their healthcare provider.
AvKARE recalled 2,192 cartons of Norgestimate and Ethinyl Estradiol tablets distributed nationwide. The recall cites failed content uniformity specifications. Consumers and healthcare providers should stop using this medicine immediately and contact AvKARE or a healthcare provider for guidance.
Canon Medical System, USA recalls 8 SPOT Fluoro digital radiography systems in the United States after a software defect could expose patients to unintended X-ray exposure. The issue occurs when the acquisition program changes and the default ROI causes the collimator and static image to partially cover the collimated area. Stop using the affected devices and follow manufacturer instructions for a
LeMaitre Vascular recalled 28 Artegraft Collagen Vascular Grafts distributed nationwide in 17 states. The grafts use bovine carotid arteries sourced from a supplier not reviewed by the appropriate regulatory authority. Patients and healthcare providers should stop using the device immediately and contact LeMaitre Vascular for instructions.
ICF Factory recalled 12 pints of Vanilla G. Nutt Ice Cream sold in New York after an undeclared almond allergen was detected. The product may contain almond not listed in ingredients. Consumers should not eat it and contact ICF Factory for refund or replacement information.
BigTree Sales recalled its BT-GERMWAND-LRG-WHT handheld UV-C germicidal wand sold in the United States after FDA enforcement flagged unsafe UVC emissions. The device reaches the exposure limit for Risk Group 3 in about 2.2 minutes, creating a risk of skin and eye injuries. Stop using the device immediately and follow the recall instructions provided by the manufacturer.
Fagron Compounding Services recalls 109,320 sterile single-dose bevacizumab syringes nationwide due to lack of assurance of sterility. Healthcare providers and patients should stop using the product immediately. Contact Fagron Compounding Services or a healthcare provider for guidance. The recall was issued on 2025-08-29 and remains active as of 2025-09-24.
Baxter Healthcare Corp. is recalling 18,720 CLEARLINK System Non-DEHP Conti-Flo Soln Sets sold nationwide in the United States. The IV sets may leak, potentially compromising therapy. Patients and healthcare providers should stop using the device immediately and contact Baxter Healthcare for instructions.
Tas Tematic Foods recalled 5 cases of Frozen Raw Easy Peel Shrimp IQF 2-lb bags after the FDA flagged high nitrofuran levels. The product was distributed to two consignee locations in California. Consumers should not consume the shrimp and should seek refunds or replacements from Tas Tematic Foods.