Device recall
Z-2043-2018: Medical Action Industries Inc. Blue OR Towel Non X-Ray Detectable (6 Towels per…
FDA device recall · Class II · Medical Action Industries Inc
Key facts
| Recall number (Z-number) | Z-2043-2018 |
|---|---|
| Recall event | 80147 |
| Product | Medical Action Industries Inc. Blue OR Towel Non X-Ray Detectable (6 Towels per Pack) / product # AVID266 Sterile This OR towel product is intended for external use only. These towels are intended to be used as absorbent towels for hand drying, cleanup, and to provide increased absorbency of blood… |
| Product code | FRL |
| Recalling firm | Medical Action Industries Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 22, 2020 |
| FEI number | 1030451 |
At a glance
- None 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