Bard Stinger Ablation Catheter: Item Numbers 210001 218501 L210001 210002 218502 L210002 210003 218503 L210003 210004 21
FDA device recall Z-0598-03 · posted 2003-02-28 · Terminated
Recall details
- Recalling firm
- C. R.Bard, Inc./Electrophysiology Division
- Reason for recall
- Sterile barrier maybe perforated compromising sterility of the device
- Action taken
- Bard Electrophysiology notified direct accounts by letter on 1.08.03 via Fed''X. Accounts are requested to return product.
- Root cause
- Packaging process control
- Status
- Terminated
- Quantity affected
- 18,706 units
- Distribution
- Nationwide
- Date initiated
- 2003-01-08
- Date posted
- 2003-02-28
- Date terminated
- 2012-05-03
- Location
- Billerica, MA
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