Bard Stinger M Ablation Catheters: Item Numbers 210001M 218501M 210002M 218502M 210003M 218503M 210004M 218504M 210005M
FDA device recall Z-0599-03 · 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
- Distribution
- Nationwide
- Date initiated
- 2003-01-08
- Date posted
- 2003-02-28
- Date terminated
- 2012-05-03
- Location
- Billerica, MA
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