Device recall
Z-1060-2022: The following first aid kits and cabinets containing components Medi-First XS…
FDA device recall · Class II · Certified Safety Mfg Inc
Key facts
| Recall number (Z-number) | Z-1060-2022 |
|---|---|
| Recall event | 89920 |
| Product | The following first aid kits and cabinets containing components Medi-First XS Non-Aspirin, Product #80450, 2 tablets/packet, 25 packets/box; and Sinus Pain & Pressure, Product #81950, 2 tablets/packet, 25 packets/box. Product number and description: (1) K614-020 16PW - Firestone Supplemental… |
| Product code | LRR |
| Recalling firm | Certified Safety Mfg Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 4, 2026 |
| 510(k) numbers | K940249 |
| FEI number | 1000158435 |
At a glance
- 1–9 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