Device recall
Z-3025-2011: GYNDisposables Inc, IUD INSERTION KIT 935K, STERILE, SINGLE USE, Tenaculum 356T…
FDA device recall · Class II · GYN Disposables Inc
Key facts
| Recall number (Z-number) | Z-3025-2011 |
|---|---|
| Recall event | 59661 |
| Product | GYNDisposables Inc, IUD INSERTION KIT 935K, STERILE, SINGLE USE, Tenaculum 356T, Uterine Sound 906S, Scissors, Povidone-Iodine Solution, (3) Swabsticks, Paper Towel, STERILE EO, REF 935K, QTY 1, GYN Disposables,Inc. 2671 Appling Road, Memphis, TN 38133, ph 901.377.2200, fx 901.377.2207 Intended for… |
| Product code | HDC |
| Recalling firm | GYN Disposables Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 29, 2012 |
| 510(k) numbers | K073182 |
| FEI number | 1000111025 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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