Device recall
Z-2213-2016: AMD-RITMED brand Conforming Stretch Gauze Bandages, Sterile, 6 in x 4/1 yds./15…
FDA device recall · Class II · Amd-Ritmed, Inc.
Key facts
| Recall number (Z-number) | Z-2213-2016 |
|---|---|
| Recall event | 73696 |
| Product | AMD-RITMED brand Conforming Stretch Gauze Bandages, Sterile, 6 in x 4/1 yds./15 cm x 3.7 cm, Reorder Number/Code D606, Bar code 6 86864 04230 3, Made in China -- Manufactured for & distributed by: AMD-RITMED INC. Montreal Quebec H8T 3J8 -- US Distribution: AMD-RITMED INC. Tonawanda, NY 14150 -- Type… |
| Product code | FQM |
| Recalling firm | Amd-Ritmed, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 15, 2016 |
| FEI number | 1319092 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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