FDA Device recall Z-0628-2023
DeRoyal KIT EXTREMITY PACK, REF 89-8869.09
- FDA Device
- Class II
- ongoing
- Published 2022-12-21
On 2022-12-21 the FDA classified a Class II recall of DeRoyal KIT EXTREMITY PACK, REF 89-8869.09 by Deroyal Industries, citing XXX.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0628-2023 |
| 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
DeRoyal KIT EXTREMITY PACK, REF 89-8869.09
Reason
XXX
Identifiers
| code_info | Lot Numbers: Lot 56390950 exp 6/1/2026; Lot 56837871 exp 9/1/2026; Lot 5718781 exp 10/1/2026 |
|---|
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-0628-2023%22
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