Device recall
Z-0305-2021: CMEAmerica BodyGuard Wall Charger: Lot number 2019-0364, Mode/Catalogue number…
FDA device recall · Class II · CME America LLC
Key facts
| Recall number (Z-number) | Z-0305-2021 |
|---|---|
| Recall event | 85479 |
| Product | CMEAmerica BodyGuard Wall Charger: Lot number 2019-0364, Mode/Catalogue number 151-143XL, *+B 01151143X L0/$$72019-0364/ 16D20191101/* Lot Number Label: BODYGUARD LOT 2019-0364 Manufacturing Date: 2019 - 11-01 , LABEL I.D. SM-0642 REV. 01, CMEAmerica Wall Charger Kit, REF 151-143XLP, Contents; Wall… |
| Product code | FRN |
| Recalling firm | CME America LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 26, 2022 |
| 510(k) numbers | K042696 |
| FEI number | 3006967710 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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