Bard * Davol Reliavac 400 Closed Wound Suction Kit * Sterile/EO * Single use * Medium-Large 3/16'' (15 Fr., 4.7mm) O.D.
FDA device recall Z-1568-05 · posted 2005-09-21 · Terminated
Recall details
- Recalling firm
- C.R. Bard, Inc., Urological Division
- Reason for recall
- An incorrect Y-connector was placed in the kit.
- Action taken
- Consignees were notified by letter on/about 08/17/2005
- Root cause
- Other
- Status
- Terminated
- Product code
- GBX
- Quantity affected
- 360 units
- Distribution
- AL, CA, FL, GA, IL, IN, NJ, TN, TX, Belgium and Japan
- Date initiated
- 2005-08-17
- Date posted
- 2005-09-21
- Date terminated
- 2009-08-21
- Location
- Covington, GA
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