Microcuff Pediatric Endotracheal Tubes - Oral Pre-Curved: ID Size: 3,0mm, Microcuff Product Reference: I-MPEDC-30; ID Si
FDA device recall Z-1264-06 · posted 2006-07-25 · Terminated
Recall details
- Recalling firm
- Microcuff Gmbh
- Reason for recall
- Inadequate seals and/or holes in the pouch may compromise the sterility of the product.
- Action taken
- A notification by telephone was made in April 2006. A confirmation letter was later sent on 6/29/2006.
- Root cause
- Other
- Status
- Terminated
- Product code
- BTR
- Quantity affected
- 1730 units (total for all three types)
- Distribution
- U.S.
- Date initiated
- 2006-06-19
- Date posted
- 2006-07-25
- Date terminated
- 2007-05-01
- Location
- Weinheim, Germany
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