Argon Medical Devices, Vesseloops, Blue Maxi, Two Latex free silicone vessel ties. Quantity: 1 box of 10 each (2 per pou
FDA device recall Z-1044-04 · posted 2004-07-20 · Terminated
Recall details
- Recalling firm
- Argon Medical Devices, Inc
- Reason for recall
- Inadequate closure compromising sterility.
- Action taken
- The recall was initiated by certified letter on 06/22/2004.
- Root cause
- Other
- Status
- Terminated
- Product code
- KDC
- Quantity affected
- 5604 units
- Distribution
- Distribution ocurred in the following states PA, MO, NJ, OH, CA, VA, NM, TX, NE, and to Tokyo, Japan.
- Date initiated
- 2004-06-22
- Date posted
- 2004-07-20
- Date terminated
- 2005-11-03
- Location
- Athens, TX
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