FDA Device recall Z-0077-2027
HALYARD Laparoscopy Comprehensive Pack II REF: 49332
- FDA Device
- Class II
- ongoing
- Published 2026-10-14
On 2026-10-14 the FDA classified a Class II recall of HALYARD Laparoscopy Comprehensive Pack II REF: 49332 by Gri Medical And Electronic Technology, citing laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0077-2027 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-08-26 |
| Published | 2026-10-14 |
| Last updated | 2026-10-21 05:30 UTC |
| Company | Gri Medical And Electronic Technology |
| Distribution | US |
Product
HALYARD Laparoscopy Comprehensive Pack II REF: 49332
Reason
Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter
Identifiers
| code_info | UDI-DI: 10680651493320 (unit level), 30680651493324 (case level) Lot Numbers: GL25271CXA-Expiry Date: 2029/3/30; GL2529…UDI-DI: 10680651493320 (unit level), 30680651493324 (case level) Lot Numbers: GL25271CXA-Expiry Date: 2029/3/30; GL25296CXA-Expiry Date: 2029/3/30; GL26076CXA-Expiry Date: 2029/5/31 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-10-21 05:30 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0077-2027%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.