FDA Device recall Z-0605-2023
GEO-MED UPPER EXTERMITY PACK, REF 89-8253.02
- FDA Device
- Class II
- ongoing
- Published 2022-12-21
On 2022-12-21 the FDA classified a Class II recall of GEO-MED UPPER EXTERMITY PACK, REF 89-8253.02 by Deroyal Industries, citing XXX.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0605-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-11-03 |
| Published | 2022-12-21 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Deroyal Industries |
| Distribution | AL, AZ, CT, FL, GA, IL, IN, KS, LA, MA, MI, MN, MO, MS, NC, NJ, NY, OH, PA, TN, TX, VA, WI |
Product
GEO-MED UPPER EXTERMITY PACK, REF 89-8253.02
Reason
XXX
Identifiers
| code_info | Lot Numbers: Lot 56189375 exp 10/1/2024; Lot 56392381 exp 10/1/2024; Lot 56618504 exp 11/1/2024; Lot 57392455 exp 2/1/2025; Lot 5775963 exp 4/1/2025 |
|---|
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-0605-2023%22
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