These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.

High Risk Recalls

2,247 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.

What to do if you own a recalled product:

  1. Stop using the product immediately
  2. Keep the product away from children
  3. Follow the remedy instructions provided
  4. Contact the manufacturer for a refund or replacement
HIGHFDA DEVICE

Medline Recalls Convenience Kits Over Sterility Concerns

Medline Industries recalled 4,757 convenience kits on January 7, 2026, due to sterilization calibration issues. The recall affects multiple models, raising concerns about sterility assurance levels. Patients and healthcare providers should stop using these products immediately.

Medline Industries, LP
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HIGHFDA DEVICE

Medline Recalls Convenience Kits Over Sterility Concerns

Medline Industries recalled 3,561 convenience kits on January 7, 2026, due to sterilization calibration issues. The recall affects multiple models, including the ENDO KIT W/SYRINGE and ANGIOGRAPHY PACK. Health providers should stop using these kits immediately.

Medline Industries, LP
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HIGHFDA DEVICE

Medline Recalls Convenience Kits Over Sterility Concerns

Medline recalled 27,320 convenience kits on January 7, 2026, due to calibration issues with sterilization equipment. These defects may compromise the sterility assurance level of the products. Healthcare providers and patients should stop using the affected kits immediately.

Medline Industries, LP
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HIGHFDA DEVICE

Medline Recalls Convenience Kits Due to Sterility Risks

Medline Industries recalled 1,496 convenience kits on January 7, 2026, due to sterilization calibration issues. The recall affects various models, potentially compromising sterility assurance levels. Patients and healthcare providers must stop using these devices immediately.

Medline Industries, LP
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HIGHFDA DEVICE

Medline Dental Pack Recalled Over Sterility Concerns

Medline Industries recalled 2,236 dental packs on January 7, 2026, due to calibration issues affecting sterilization. The recall impacts products distributed worldwide, raising safety concerns for healthcare providers. Consumers should stop using the recalled items immediately and follow manufacturer instructions.

Medline Industries, LP
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HIGHFDA DEVICE

Medline Recalls Arthroscopy Kits Over Sterility Concerns

Medline Industries recalled 175 arthroscopy kits on January 7, 2026. Calibration issues with sterilization equipment may impact product sterility. Patients and healthcare providers should stop using the devices immediately.

Medline Industries, LP
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HIGHFDA DEVICE

Medline Recalls Nerve Block Tray Over Sterility Concerns

Medline Industries recalled 448 units of its BASIC NERVE BLOCK TRAY W/LINEN on January 7, 2026. The recall stems from calibration issues with sterilization equipment that may affect the product's sterility assurance level. Healthcare providers should stop using the device immediately and follow the provided instructions.

Medline Industries, LP
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HIGHFDA DEVICE

Medline Convenience Kits Recalled Due to Sterility Issues

Medline Industries recalled 30,958 convenience kits on January 7, 2026. Calibration issues with sterilization equipment may compromise product sterility. Healthcare providers and patients must stop using these products immediately.

Medline Industries, LP
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HIGHFDA DEVICE

Medline Recalls Urology Kits Over Sterility Issues

Medline Industries recalled 59 urology convenience kits on January 7, 2026, due to sterilization calibration issues. These defects may compromise the sterility assurance level of the devices. Patients and healthcare providers should immediately stop using these products and follow recall instructions.

Medline Industries, LP
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HIGHFDA DEVICE

Medline Surgical Drapes Recalled Over Sterility Issues

Medline Industries recalled 14.9 million surgical drapes on January 7, 2026. Calibration issues with sterilization equipment may impact sterility assurance levels. Patients and healthcare providers must stop using these products immediately.

Medline Industries, LP
Medline has
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HIGHFDA DEVICE

Medline Convenience Kits Recalled Over Sterility Issues

Medline Industries, LP recalled 154,427 Convenience Kits on January 7, 2026. The recall stems from calibration issues with sterilization equipment, potentially affecting sterility assurance. Patients and healthcare providers should stop using the affected products immediately.

Medline Industries, LP
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HIGHFDA DEVICE

Medline Convenience Kits Recalled Due to Sterilization Issues

Medline Industries recalled 150 units of its Convenience Kits on January 7, 2026. Calibration issues with sterilization equipment may affect the sterility assurance level of the products. Patients and healthcare providers must stop using the devices immediately.

Medline Industries, LP
Medline has
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HIGHFDA DEVICE

Medline Convenience Kits Recalled Due to Sterility Issues

Medline Industries has recalled 779 units of its Convenience Kits due to calibration issues with sterilization equipment. The recall affects multiple model numbers including DYNJ56436A and DYNJ56436B. Consumers should stop using these products immediately and follow recall instructions.

Medline Industries, LP
Medline has
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HIGHFDA DEVICE

Medline Recalls Surgical Kits Over Sterility Assurance Issues

Medline Industries recalled 4,525 surgical convenience kits on January 7, 2026, due to sterilization calibration issues. These problems could compromise sterility assurance levels, posing health risks. Healthcare providers and patients must stop using these products immediately.

Medline Industries, LP
Medline has
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HIGHFDA DEVICE

Medline Recalls Surgical Kits Due to Sterility Assurance Issues

Medline Industries recalled 117,907 surgical convenience kits on January 7, 2026, due to sterilization calibration issues. The recall affects numerous models, including spinal and knee procedure kits. Patients and healthcare providers should stop using these devices immediately.

Medline Industries, LP
Medline has
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HIGHFDA DEVICE

Medline Surgical Kits Recalled Over Sterility Assurance Issues

Medline Industries recalled 4,853 surgical kits on January 7, 2026 due to potential sterility issues. Calibration problems with sterilization equipment could affect safety. Patients and providers must stop using these kits immediately.

Medline Industries, LP
Medline has
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HIGHFDA DEVICE

Medline Surgical Kits Recalled Over Sterilization Issues

Medline Industries recalled 4,415 surgical kits on January 7, 2026, due to sterilization calibration issues. These issues could compromise the sterility assurance level of the products. Healthcare providers and patients must stop using the kits immediately.

Medline Industries, LP
Medline has
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HIGHFDA DEVICE

Medline Surgical Packs Recalled Over Sterility Concerns

Medline Industries recalled 193,157 surgical packs on January 7, 2026, due to sterility assurance issues. The recall affects two model numbers: DYNJP1050UG and DYNJP8401. Healthcare providers and patients must stop using these products immediately.

Medline Industries, LP
Medline has
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HIGHFDA DEVICE

Medline Convenience Kits Recalled Over Sterility Issues

Medline recalled 5,346 convenience kits on January 7, 2026, due to sterilization calibration issues. The recall affects multiple model numbers, potentially compromising their sterility assurance. Healthcare providers and patients must stop using the products immediately.

Medline Industries, LP
Medline has
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