FDA Device recall Z-1646-2023
Procedure packs: (1) Medline Sterile Arthroscopy Pack, REF: DYNJ64242B
- FDA Device
- Class II
- ongoing
- Published 2023-06-07
On 2023-06-07 the FDA classified a Class II recall of Procedure packs: (1) Medline Sterile Arthroscopy Pack, REF: DYNJ64242B by Medline Industries Northfield, citing the kits were damaged by water.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1646-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-04-21 |
| Published | 2023-06-07 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medline Industries Northfield |
| Distribution | CA |
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
The kits were damaged by water.
Identifiers
| code_info | (1) Arthroscopy Pack - Lot #22HMD098, Exp. 2024-04-30, UDI/DI (01)10193489956405; (2) Shoulder Pack -Lot #22JMA673, Exp…(1) Arthroscopy Pack - Lot #22HMD098, Exp. 2024-04-30, UDI/DI (01)10193489956405; (2) Shoulder Pack -Lot #22JMA673, Exp. 2024-01-31, GTIN (01)10193489429817; and (3) Upper Extremity Pack - Lot #HMF900, Exp. 2024-01-31, UDI/DI (01)10193489968453. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1646-2023%22
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