Boston Scientific Microvasive Radial Jaw 3 Single-Use Maximum Capacity Biopsy Forceps Needle, 240 cm length, 3.3 mm Jaw
FDA device recall Z-0562-03 · posted 2003-02-21 · Terminated
Recall details
- Recalling firm
- Symbiosis Corp.
- Reason for recall
- Product does not have the needle component as part of the jaw assembly.
- Action taken
- The firm forwarded recall letters and response forms via Federal Express to Risk Managers at hospitals on 9/3/2002. Accounts were asked to return product by first calling 1-800-862-1284.
- Root cause
- Other
- Status
- Terminated
- Quantity affected
- 155/5-pack
- Distribution
- Product was distributed to 29 hospital accounts nationwide. There were no intenational, govenment or military accounts.
- Date initiated
- 2002-09-03
- Date posted
- 2003-02-21
- Date terminated
- 2008-04-15
- Location
- Miami, FL
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