FDA Medical Device Recalls (openFDA)
MEDLINE INDUSTRIES, LP - Northfield: ANESTHESIA TURNOVER KIT, Pack Number DYNJAA0377
- Recall number
- Z-3071-2024
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Product
- ANESTHESIA TURNOVER KIT, Pack Number DYNJAA0377
- Status
- Open, Classified
- Initiated
- 2024-06-18
- Posted
- 2024-09-06
- Terminated
- not on file
- Reason
- A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that the user assumes sterility during its use, there is an increased risk of patient infection.
- Root cause
- Process change control
- Action
- Medline Industries issued a Recall notice to its consignees on 06/18/2024 via email. The notice explained the issue, potential risk, and directed the product to be stickered to instruct the used to remove the recalled component from the kit and replace from sterile supply. Distributors or those who have transferred the product were directed to notify those to whom the product was distributed of the recall. For questions, contact the Recall Department at 866-359-1704 or recalls@medline.com.
- Quantity
- 105 units
- Distribution
- US: TX, IL, CA
- Lot, serial or model codes
- UDI/DI Case 40195327231126, UDI/DI Each 10195327231125; Lot Numbers: 22LBM357
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- OJH
- Firm FEI
- 1417592
- Firm city
- Northfield
- Firm state
- IL
- 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