FDA Medical Device Recalls (openFDA)
Medical Action Industries, Inc. 306: Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20 packages/box, 12 boxes/case, sterile.
- Recall number
- Z-0765-2023
- Recalling firm
- Medical Action Industries, Inc. 306
- Product
- Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20 packages/box, 12 boxes/case, sterile.
- Status
- Terminated
- Initiated
- 2022-10-12
- Posted
- 2022-12-22
- Terminated
- 2025-02-19
- Reason
- Scissors contained debris.
- Root cause
- Under Investigation by firm
- Action
- The recalling firm issued letters dated 10/12/2022 via email on 10/12/2022. The letter identified the affected product, the reason for recall, and requested the consignee review their inventory and segregate and quarantine all affected product. If any of the product is found, the consignee is to discard it. If the product was further distributed, the consignee is to ensure all end users are appropriately notified of the field correction. A Field Action response Form was to be completed and returned via email as soon as possible to indicate they have read and understand the recall instructions, checked their stock and reported the quantity of product on hand, and notified their appropriate staff of any customers of the notification.
- Quantity
- 145 cases (240 scissors/case)
- Distribution
- Distribution was made to FL, IL, IN, MA, MD, MO, OH, and VA. There was no foreign/government/military distribution.
- Lot, serial or model codes
- Lot #297668, UDI 10809160003473.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- KDC
- Firm FEI
- 1030451
- Firm city
- Arden
- Firm state
- NC
- 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