Device recall
Z-2819-2015: Zimmer, Reprocessed Zimmer Tourniquet Cuffs,34" Single Hose Single Bladder Brown…
FDA device recall · Class II · STERILMED, INC.
Key facts
| Recall number (Z-number) | Z-2819-2015 |
|---|---|
| Recall event | 72035 |
| Product | Zimmer, Reprocessed Zimmer Tourniquet Cuffs,34" Single Hose Single Bladder Brown (PLC), 34", Model (Reprocessor) Number: ZIM60-7075-106, Reprocessed by Sterilmed. Products are individually packaged in a Tyvek/poly pouch. There are 5 pouches placed inside a casepack box. Each sales unit (casepack)… |
| Product code | KCY |
| Recalling firm | STERILMED, INC. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 11, 2016 |
| FEI number | 3001237663 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database