FDA Device Recalls

Recalls /

#70881

Product

HydraGlide Heparin Coated Silicone Thoracic Catheters - Straight, Atrium Code # 14124, Size (Fr) 24, # Eyelets 6, 10 per case

FDA product code
GBZCatheter, Cholangiography
Device class
Class 1
Medical specialty
General, Plastic Surgery
Affected lot / code info
Lot #s 10304308, 10311258, 10327153

Why it was recalled

Heparin-coated Thoracic Catheters were manufactured with heparin allegedly contaminated with oversulfated chondroitin sulfate

Root cause (FDA determination)

Nonconforming Material/Component

Action the firm took

Atrium Medical issued a press release on 5/12/2008 and notified consignees by facsimile on 5/12/2008. Customers were instructed to contact the firm for a return goods authorization and to notify the firm upon receipt of the recall notice.

Recalling firm

Firm
Atrium Medical Corporation
Address
5 Wentworth Dr, Hudson, New Hampshire 03051-4929

Distribution

Distribution pattern
Worldwide Distribution: USA, US Virgin Islands, South Africa, Austria, Taiwan, Venezuela, and Saudi Arabia.

Timeline

Recall initiated
2008-05-12
Posted by FDA
2008-08-14
Terminated
2009-08-20
Status

Source: openFDA Device Recall endpoint. Recall record ID #70881. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

— recall: HydraGlide Heparin Coated Silicone Thoracic Catheters - Straight, Atrium Code # 14124, Size (Fr) 24, · FDA Device Recalls