All Product Recalls

Browse through 1,551 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

HIGHFDA FOOD

Moonlight Packing Recalls Peaches Over Listeria Contamination Risk

Moonlight Packing Corp. recalled 483,973 cases of yellow peaches on October 28, 2025, due to potential Listeria contamination. Consumers should not consume the product and are advised to seek refunds. The peaches were distributed across multiple states and in Canada and Mexico.

Moonlight Packing
Potential contamination
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HIGHFDA FOOD

Moonlight Packing Recalls Yellow Peaches Over Listeria Risk

Moonlight Packing Corporation recalled 237,656 cases of yellow peaches on October 28, 2025, due to potential Listeria monocytogenes contamination. The recall affects multiple states across the U.S. and extends to Canada and Mexico.

Moonlight Packing
Potential contamination
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HIGHFDA FOOD

Moonlight Packing Recalls Peaches Over Listeria Risk

Moonlight Packing Corporation recalled 570 cases of Peppermint Peach on October 28, 2025, due to potential contamination with Listeria monocytogenes. The recall affects peaches distributed in multiple states across the U.S. Consumers should not consume affected products and seek refunds.

Moonlight Packing
Potential contamination
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HIGHFDA FOOD

Moonlight Packing Recalls Peaches Due to Listeria Risk

Moonlight Packing Corporation recalled 2,375 cases of loose bulk white peaches on October 28, 2025. The recall stems from potential contamination with Listeria monocytogenes, a bacterium that can cause severe illness. Consumers should not consume the product and should seek a refund or replacement.

Moonlight Packing
Potential contamination
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HIGHFDA FOOD

Moonlight Packing Recalls Yellow Peaches for Listeria Risk

Moonlight Packing Corporation recalled over 102,000 cases of yellow peaches on October 28, 2025. The recall follows potential contamination with Listeria monocytogenes. The affected peaches were distributed across multiple U.S. states and in Canada and Mexico.

Moonlight Packing
Potential contamination
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HIGHFDA DEVICE

Medline Recalls Adhesive Bandages Over Sterility Concerns

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.

Medline Industries, LP
Medline has
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HIGHFDA FOOD

Whatcom Blue Sliced Cheese Recalled for E. Coli Contamination

Whatcom Blue Sliced Cheese was recalled on October 27, 2025, due to potential E. coli contamination. The recall affects 411 lbs of cheese sold at Whole Foods Market in Washington and Oregon. Consumers should not consume the product and seek a refund or replacement.

WFM Purchasing, LP
Twin Sisters
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HIGHFDA FOOD

Whatcom Farmhouse Cheese Recalled Over E. Coli Contamination

Whatcom Farmhouse recalled 411 lbs of cheese products on October 27, 2025, due to potential E. coli O103 contamination. Testing by WSDA revealed the risk of STEC bacteria. The affected cheese was sold at Whole Foods Market locations in Washington and Oregon.

WFM Purchasing, LP
Twin Sisters
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HIGHFDA DEVICE

Medline Recalls Adhesive Bandages Due to Sterility Concerns

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.

Medline Industries, LP
Medline has
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HIGHFDA DEVICE

Nipro Medical Hemodialysis System Recalled Due to Screw Hazard

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.

Nipro Medical
Screw may
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HIGHFDA DEVICE

Medline Recalls Perfusion Syringe Due to Biocompatibility Issues

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.

Medline Industries, LP
Medline Industries,
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HIGHFDA DEVICE

Medline Recalls Curad Bandages Due to Sterility Risk

Medline Industries recalled 18,000 units of Curad Quick Strip Fabric Bandages on October 27, 2025. The recall affects all lots due to compromised seals that may affect sterility. Consumers should stop using these bandages immediately and follow recall instructions.

Medline Industries, LP
Medline has
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HIGHFDA DEVICE

Philips Recalls Azurion 7 M20 X-ray System Over Safety Concern

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.

Philips North America
Between July
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HIGHFDA DEVICE

Medline Recalls Adhesive Bandages Over Sterility Concerns

Medline Industries recalled 1.57 million units of Curad Touch-Free and Quick-Strip Bandages on October 27, 2025. The packaging may exhibit open seals, compromising sterility. Consumers should stop use immediately and follow the recall instructions provided by the manufacturer.

Medline Industries, LP
Medline has
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HIGHFDA DEVICE

Medline Recalls Adhesive Bandages Over Sterility Concerns

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.

Medline Industries, LP
Medline has
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HIGHFDA DEVICE

Medline Recalls Adhesive Bandages Over Sterility Concerns

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 Industries, LP
Medline has
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HIGHFDA DEVICE

Medline Recalls CURAD Germ-Shield Bandages Over Sterility Risk

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, LP
Medline has
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HIGHFDA FOOD

MeriCal Recalls Super Greens Supplement Due to Salmonella Risk

MeriCal, LLC recalled 698,064 units of its Super Greens Dietary Supplement on October 24, 2025. The recall follows potential contamination with Salmonella Richmond. Consumers should not consume the product and seek refunds immediately.

MeriCal
Potential contamination
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HIGHFDA DEVICE

Siemens Recalls MAMMOMAT Inspiration Operator Tables Due to Hazard

Siemens Medical Solutions USA recalled six MAMMOMAT Inspiration operator tables on October 24, 2025. The operator tables were sold with a bus-installation kit, which they are not designed for. This recall affects three units in the U.S. and three internationally.

Siemens Medical Solutions USA
There were
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