FRAZIER Surgical Suction Instrument, 5 French with Control Vent and Obturator, Product Code: 0031050, 50/C. STERILE, EO, Rx ONLY. MANUFACTURED FOR CONMED CORPORATION 310 Broad Street, Utica, NY 13501
FDA Recall Z-0556-2008 · Posted 2008-02-02
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Recalling FirmConmed Corporation
Recall StatusTerminated
Product CodeGCJ
Date Initiated2007-09-12
Date Terminated2012-08-30
Product Quantity34,738 instruments
Reason for Recall
Sterility (package integrity) compromised -- Frazier and Poole suction instruments may have an inadequate seal. The product pouch seal made during assembly of this product, may be incomplete or not present.
Firm Action
URGENT-Device Recall Letters (dated 9/10/07) and FIELD CORRECTIVE ACTION CERTIFICATION forms were sent via Certified Mail to affected customers the week of 9/09/07 (mailed on 9/12/07). The recall letters informed the consignees of the recall due to potentially inadequate seals of the instruments, and instructed them to review their inventory of the instruments checking them for inadequate seals. The letters also instructed the consignees to complete the form and fax it back by 9/21/07. For those consignees that have any of the recalled instruments or may have questions, please contact ConMed Quality Assurance at 1-800-552-0138 ext. 5225 between the hours of 7 am - 6 pm (MST). International customers were notified on 9/18/07. A second recall letter (dated 10/09/07) was sent to non-respondents of the initial mailing. ConMed plans to send a third recall letter to the non-responders during the week of 12/10/07 which addresses sub-recall notifications to the distributors' customers.
Root Cause
Packaging process control
Distribution Pattern
Nationwide and Worldwide Distribution
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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