Recalls / —
—#70882
Product
HydraGlide Heparin Coated Silicone Thoracic Catheters - Straight, Atrium Code # 14132, Size (Fr) 32, # Eyelets 6,
- FDA product code
- GBZ — Catheter, Cholangiography
- Device class
- Class 1
- Medical specialty
- General, Plastic Surgery
- Affected lot / code info
- Lot #s 10304309, 10318735, 10344304
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 #70882. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.