FDA Device recall Z-0922-2026
FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048
- FDA Device
- Class II
- ongoing
- Published 2025-12-24
On 2025-12-24 the FDA classified a Class II recall of FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048 by Medline Industries, citing the items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0922-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-11-13 |
| Published | 2025-12-24 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries |
| Distribution | US |
Product
FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048
Reason
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
Identifiers
| code_info | DYNJ04048, UDI-DI: 10193489195248(each), 20193489195245(case), Lot Number: 2023112290 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0922-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.