Curity" X-Ray Detectable Laparotomy Sponges, Soft Pouch Pack, 8" x 36" (20.3 cm x 91.4 cm) Item Number: 6556
FDA device recall Z-1857-2016 · posted 2016-05-31 · Terminated
Recall details
- Recalling firm
- Covidien LLC
- Reason for recall
- Compromised sterility due to breach of barrier
- Action taken
- Covidien initiated recall by letter on March 4, 2016. Customers were notified via Federal Express and the letter instructs customers to discontinue use of the product and return all inventory to Medtronic (Covidien), 195 McDermott Road, North Haven, CT 06473, Attention: Field Returns Department. Any questions or concerns, contact your Medtronic representative or Customer Service at (800) 882-5878
- Root cause
- Packaging process control
- Status
- Terminated
- Product code
- LRS
- Quantity affected
- 87680
- Distribution
- Distributed US (nationwide) and the countries of Canada, Austria, Belgium, Columbia, Croatia, France, Germany, Guadeloupe, Ireland, Italy, La Reunion, New Zealand, Norway, Poland, Portugal, Saudi Arab
- Date initiated
- 2016-03-03
- Date posted
- 2016-05-31
- Date terminated
- 2017-06-15
- Location
- North Haven, CT
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