medical MODERATE Updated 2026-08-12

Boston Scientific Corporation recalls Radial Jaw 4 Jumbo Biopsy Forceps with the following descrip

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Recalled Product

Radial Jaw 4 Jumbo Biopsy Forceps with the following descriptions and UPN: Radial Jaw 4 Jumbo 240cm Box 5; Outer Box UPN: M00513363; Inner Box UPN: M00513360.

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Hazard / Issue

Potential for breach in sterile barrier of device packaging.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Outer Box UPN: M00513363; Inner Box UPN: M00513360. GTIN: 08714729761914. Lot Number: 38496094.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Radial Jaw 4 Jumbo →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

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