Procedure packs: — Class II medical device recall Z-1646-2023
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2023-06-07, distributed in CA. The kits were damaged by water.
| Recall number | Z-1646-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2023-04-21 |
| Classified | 2023-05-26 |
| Reported by FDA | 2023-06-07 |
| Distributed | CA |
| UPC / GTIN / UDI-DI | 10193489429817, 10193489956405, 10193489968453 |
| Lot numbers | 22HMD098, 22JMA673, HMF900 |
| Model numbers | DYNJ64242B, DYNJ64250A, DYNJ64253B |
| Expiration dates | 2024-01-31, 2024-04-30 |
Product
Procedure packs: (1) Medline Sterile Arthroscopy Pack, REF: DYNJ64242B; (2) Medline Sterile Shoulder Pack, REF: DYNJ64250A; and (3) Medline Sterile Upper Extremity Pack, REF: DYNJ64253B.
Reason for recall
The kits were damaged by water.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1646-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.