NOVAPLUS Electrosurgical Grounding Pads, Split with Cord Catalog No. 7179V
FDA device recall Z-0037-05 · posted 2004-10-22 · Terminated
Recall details
- Recalling firm
- 3M Company / Medical Division
- Reason for recall
- Improper wire placement from the patient plate to the ESU connector plug results in an intermittent displacement connection.
- Action taken
- A recall notification letter dated 09/30/2004 was sent to Hospitals and Health Care Distributors instructing consignees to immedately remove all effective product from lot 2007-06 HP.
- Root cause
- Other
- Status
- Terminated
- Product code
- JOS
- Quantity affected
- 384 cases containing 40 pads each for a total of 15,360 pads
- Distribution
- The subject product lot was distributed to the following key 3M distributors: Owens & Minor, Cardinal Health, McKesson, Professional Health Supply, and the Burrows Company.
- Date initiated
- 2004-09-30
- Date posted
- 2004-10-22
- Date terminated
- 2005-11-14
- Location
- South St Paul, MN
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| 3M SCOTCHPLATE II DISPERSIVE ELECTRODE (K833364) | 3M Company | 1983-11-29 |