Device recall
Z-1591-2011: Anchor Tissue Retrieval System; ETO sterilized, single use disposable device…
FDA device recall · Class II · Anchor Products Company, Inc.
Key facts
| Recall number (Z-number) | Z-1591-2011 |
|---|---|
| Recall event | 57432 |
| Product | Anchor Tissue Retrieval System; ETO sterilized, single use disposable device; port size 15 mm, 1550 mL capacity; 3 units per box; Manufacturer: Anchor Products Co., 52 Official Rd, Addison, IL 60101 U.S.A.; Ref TRS175SB The device is a single use, sterile disposable pouch used with a dedicated… |
| Product code | GCJ |
| Recalling firm | Anchor Products Company, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 20, 2012 |
| 510(k) numbers | K061555 |
| FEI number | 1416891 |
At a glance
- 1–9 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