Device recall
Z-1968-2011: Lube Jelly, 1 oz. water-base sterile lubricating jelly, a component of various…
FDA device recall · Class II · Cardinal Health
Key facts
| Recall number (Z-number) | Z-1968-2011 |
|---|---|
| Recall event | 58054 |
| Product | Lube Jelly, 1 oz. water-base sterile lubricating jelly, a component of various Presource Custom Sterile Convenience Packs/Modules; Packaged by Cardinal Health Medical Products and Services, McGaw Park, IL 60085 U.S.A.; The affected lots of modules actually contain a 1 oz. tube of Non-Sterile Kendall… |
| Product code | KMJ |
| Recalling firm | Cardinal Health |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 19, 2012 |
| FEI number | 3001236905 |
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