Device recall
Z-1055-2014: CATH ANGIOGRAPHY DRAPE PACK; REF: DYNJ40851; Packaged in Mexico for Medline…
FDA device recall · Class I · Medline Industries, Inc.
Key facts
| Recall number (Z-number) | Z-1055-2014 |
|---|---|
| Recall event | 66080 |
| Product | CATH ANGIOGRAPHY DRAPE PACK; REF: DYNJ40851; Packaged in Mexico for Medline Industries, Inc., Mundelein, IL 60060; 1-800-Medline; www.medline.com Surgical kit used to supply tools required to perform medical procedures. |
| Product code | LRO |
| Recalling firm | Medline Industries, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Dec 19, 2017 |
| FEI number | 3000717925 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 1,000+ 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