Medical Device Recall: Z-0037-05

FDA Recalls dataset · Firm: N/A · Status: Terminated

Recall Action Class: N/A Date Initiated: 2004-09-30 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0037-05.

Recall Res Number
Z-0037-05
Recalling Firm / Manufacturer
N/A
FEI Number
2110898
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2004-09-30
Date Posted
2004-10-22
Date Terminated
2005-11-14
Product Code
JOS
Event Number
30137
Product Quantity
384 cases containing 40 pads each for a total of 15,360 pads
Product Description NOVAPLUS Electrosurgical Grounding Pads, Split with Cord Catalog No. 7179V
Reason for Recall Improper wire placement from the patient plate to the ESU connector plug results in an intermittent displacement connection.
Action Details 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.
Distribution Pattern The subject product lot was distributed to the following key 3M distributors: Owens & Minor, Cardinal Health, McKesson, Professional Health Supply, and the Burrows Company.
Code Information / Serial Numbers Lot 2007-06 HP

Related Establishments / Registrations

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