2,153 recalls tagged with “stop use immediately”.
Agebox recalled its iKids-Growth Night Formula due to the presence of undeclared ibutamoren. The recall affects 60-count bottles manufactured exclusively for AGEBOX Inc. Consumers should stop using the product immediately and contact Agebox or their healthcare provider for guidance.
Moonlight Packing Corporation recalled 2,622 cases of sticker labels for loose bulk peppermint peaches on October 28, 2025. The recall stems from potential contamination with Listeria monocytogenes. Consumers should not consume this product and should contact the company for a refund or replacement.
Illumina recalled 11,916 NextSeq 550Dx reagent kits and flow cells worldwide after identifying a gasket defect that can leak during sequencing. The issue may cause run failures, no or insufficient data output, instrument fluidics clogs and potential exposure to toxic substances. Healthcare providers and users should stop using the affected kits and await recall instructions from Illumina.
Baxter Healthcare recalled 118 units of the Welch Allyn INF BAG, Model REF 5089-18, on October 28, 2025. The replacement bladder may contain a Large Adult size bladder instead of a Thigh size bladder. This defect poses a high risk for inaccurate blood pressure readings.
Medline Industries, LP recalled 15 units of its perfusion syringe on October 27, 2025, due to potential biocompatibility failures. These failures may lead to risks of irritation and other serious health issues. Healthcare providers and patients must stop using the product immediately and follow the recall instructions.
Nipro Medical Corporation recalled the Surdial DX Hemodialysis System on October 27, 2025, after reports of screws loosening and potentially falling out. The recall affects devices distributed nationwide across 19 states. Patients and healthcare providers must stop using the device immediately and follow manufacturer guidance.
Twin Sisters Creamery recalled 411 pounds of Whatcom Blue Sliced Cheese sold by Whole Foods Market through distributor Peterson Company in Washington and Oregon. WSDA testing identified potential STEC and E. coli O103 contamination. Consumers who bought the cheese should not eat it and should contact WFM Purchasing, LP for a refund or replacement.
Medline Industries recalled 182,526 units of CURAD Germ-Shield Touch-Free Fabric Bandages due to compromised sterility. The recall affects all lots manufactured and distributed in the US, Guam, Canada, and the UAE. Consumers must stop using these bandages immediately.
Medline Industries recalled 6,989,900 units of Quick Strip Fabric Sterile Adhesive Bandages on October 27, 2025. The recall stems from open seals in the packaging that may compromise sterility. Patients and healthcare providers should stop using these products immediately.
Medline recalled 4.4 million Quick Strip Plastic Sterile Adhesive Bandages on October 27, 2025. The recall affects all lots due to potential open seals compromising sterility. Consumers and healthcare providers should stop using these bandages immediately.
Philips North America recalled 110 Azurion 7 M20 interventional fluoroscopic X-ray systems on October 27, 2025. These devices were shipped without the necessary Source-to-Skin Distance (SSD) Spacer, violating FDA regulations. The absence of this spacer poses a serious health risk during fluoroscopy applications.
Medline Industries recalled 1,725,600 units of Quick Strip Plastic Sterile Adhesive Bandages due to potential packaging defects. The recall, issued on October 27, 2025, affects all lots of Curad Touch-Free and Quick-Strip Bandages. Open seals may compromise the sterility of the product, posing a health risk.
Twin Sisters Creamery recalled 411 pounds of Whatcom Farmhouse cheese sold through Whole Foods Market after testing flagged potential STEC and E. coli O103 contamination. The recall is Class I. Consumers who bought this product should not eat it and should contact WFM Purchasing, LP for refund or replacement information.
Medline Industries recalled 11,291,800 units of Quick Strip Fabric Sterile Adhesive Bandages on October 27, 2025. The recall affects all lots due to potential open seals that compromise sterility. Consumers should stop using these bandages immediately.
EDAN recalled 395 units of its Central Monitoring System on October 24, 2025, due to potential cybersecurity risks. The affected models include MFM-CNS and MFM-CNS Lite, which manage critical fetal and maternal health data. Healthcare providers must stop using the devices immediately and follow the recall instructions.
EDAN recalled 3,824 Patient Monitors on October 24, 2025. The recall follows an FDA letter regarding cybersecurity vulnerabilities. Affected models include X8, X10, and X12, distributed nationwide and to Mexico.
EDAN recalled 379 patient monitors on October 24, 2025, due to potential cybersecurity issues. Models iX10, iX12, and iX15 pose risks to patient safety. Healthcare providers should stop using these devices immediately.
MeriCal recalled 698,064 units of Member's Mark Super Greens Dietary Supplement sold nationwide. The recall is due to potential contamination with Salmonella Richmond. Consumers should not consume the product and should contact MeriCal for refund or replacement information via email.
EDAN recalled 3,141 patient monitors on October 24, 2025, due to potential cybersecurity vulnerabilities. The recall affects models iM8, iM8A, and iM8B used for monitoring physiological parameters. Healthcare providers must stop using these devices immediately and follow the manufacturer's instructions.
EDAN recalled 3,721 fetal monitors on October 24, 2025, due to potential cybersecurity vulnerabilities. The affected models, F2 and F3, are used to monitor pregnant women and fetuses after 28 weeks of gestation. Healthcare providers must stop using these devices immediately and follow recall instructions.