FDA Medical Device Recalls (openFDA)
Boston Scientific Corporation: Boston Scientific Radial Jaw 4 Large Capacity w/Needle Biopsy Forceps Box 80, 240cm UPN/Catalog Number: M00513334
- Recall number
- Z-1773-2010
- Recalling firm
- Boston Scientific Corporation
- Product
- Boston Scientific Radial Jaw 4 Large Capacity w/Needle Biopsy Forceps Box 80, 240cm UPN/Catalog Number: M00513334
- Status
- Terminated
- Initiated
- 2010-05-06
- Posted
- 2010-06-04
- Terminated
- 2011-09-20
- Reason
- Clevis may detach from the coil preventing the device to open and/or close. Delays in the procedure may result.
- Root cause
- Process control
- Action
- Boston Scientific issued Recall notification letters via Federal Express Priority mail on May 6, 2010. The notification instructs the account to check their inventory, remove any affected product from their inventory, and return it to Boston Scientific. The notification also requests the completion of a Reply Verification Tracking Form as a method of documenting the presence or absence of affected product from their inventory. In the letter, customers with questions are provided with a phone and email at the firm to contact.
- Quantity
- not on file
- Distribution
- Nationwide; Panama.
- Lot, serial or model codes
- Lots: 13361332, 13361334
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FCL
- Firm FEI
- 3005099803
- Firm city
- Marlborough
- Firm state
- MA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28