FDA Medical Device Recalls (openFDA)
MEDLINE INDUSTRIES, LP - Northfield: Total Hip Kit, REF DYNJ903275S; surgical convenience kit
- Recall number
- Z-2366-2023
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Product
- Total Hip Kit, REF DYNJ903275S; surgical convenience kit
- Status
- Open, Classified
- Initiated
- 2023-07-03
- Posted
- 2023-08-10
- Terminated
- not on file
- Reason
- The prep solution included in the Total Hip Kit expires prior to the expiration date of the Kit.
- Root cause
- Under Investigation by firm
- Action
- Medline notified its sole consignee by email on 07/07/2023, The consignee was instructed to destroy any affected product that they may have on hand.
- Quantity
- 16 kits
- Distribution
- US Nationwide distribution in the state of Illinois.
- Lot, serial or model codes
- UDI/DI: 10195327254582 (unit), 40195327254583 (case); Lot code 23CDC733
- 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