Device recall
Z-1476-2022: Medline Custom procedural kits labeled as follows: a. GP-NEURO PACK, b. KIT NEUR…
FDA device recall · Class II · MEDLINE INDUSTRIES, LP - SPT
Key facts
| Recall number (Z-number) | Z-1476-2022 |
|---|---|
| Recall event | 90516 |
| Product | Medline Custom procedural kits labeled as follows: a. GP-NEURO PACK, b. KIT NEUR FUS LUM POST, c. KIT PEDI VP SHUNT, d. KIT STC NEURO SPINE GENERIC, e. MAIN BASIC NEURO, f. MAJOR NEURO PK-LF, g. NEURO, h. NEURO CERVICAL PACK, i. NINOR NEURO PK-LF, j. VP SHUNT PACK Model/Catalog Number: Model… |
| Product code | OJG |
| 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
- 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