Applied Blunt Tip Trocar Models C0717 and C0718
FDA device recall Z-0009-05 · posted 2004-10-05 · Terminated
Recall details
- Recalling firm
- Applied Medical Resources Corp
- Reason for recall
- Inadequate trocar tip assembly that might yeild parts to patients.
- Action taken
- Initiated recall by letter on 9/16/2004 via Fedex/UPS. Follow-up to nonresponders in 30 days.
- Root cause
- Other
- Status
- Terminated
- Product code
- KXN
- Quantity affected
- 1025
- Distribution
- Nationwide. Ireland.
- Date initiated
- 2004-09-17
- Date posted
- 2004-10-05
- Date terminated
- 2005-08-05
- Location
- Rancho Santa Margarita, CA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| TROCAR W/ BLUNT TIP OBTURATOR (K923636) | Applied Medical Resources | 1993-11-05 |