Device recall
Z-1474-2022: Medline Convenience kits labeled as: a. MAJOR VASCULAR CDS, b. POST OP KIT, c…
FDA device recall · Class II · MEDLINE INDUSTRIES, LP - SPT
Key facts
| Recall number (Z-number) | Z-1474-2022 |
|---|---|
| Recall event | 90516 |
| Product | Medline Convenience kits labeled as: a. MAJOR VASCULAR CDS, b. POST OP KIT, c. KIT NEURO FUS LUM POST SANSUR, d. KIT NEURO FUS LUM POST SANSUR , e. PRE-OP ACCESSORY KIT CHOICE, f. DEEP BRAIN STIMULATION PACK, g. DEEP BRAIN STIMULATION PACK, h. MINIMALLY INVASIVE PACK-LF, i. EVLP Pack/Kit, j. GENERAL… |
| Product code | LRO |
| Recalling firm | MEDLINE INDUSTRIES, LP - SPT |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3000717925 |
At a glance
- None Linked 510(k)s
- 1–9 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