Recall Z-1081-2010
Integra LifeSciences Corp · initiated January 13, 2010
Product
Suturable DuraGen Dural Regeneration Matrix; Non-Pyrogenic; Sterility guaranteed unless package is damaged or opened. Rx only. Manufacturer: Integra LifeSciences Corporation, Plainsboro, NJ 08536 Suturable DuraGen is an absorbable implant for repair of dural defects. It is indicated as a dural substitute for the repair of dura matter.
Codes / lots: Catalog Number DURS3391; Lot number 1091575
Reason for recall
One lot of Suturable DuraGen Dural Regeneration Matrix (# 1091575) did not pass stability testing at certain time points for Suture Retention Strength and Shrink Temperature specifications.
FDA-determined cause: Other
Action taken
An "URGENT PRODUCT RECALL NOTIFICATION" dated January 13, 2010, was sent via Federal Express to customers. The notification described the product, problem, hazard involved and action to be taken by customers. In the event that the customers have in their possession any products from the specific lot number 1091576, the customers are being ask to please immediately quarantine all stock on hand and contact their local Integra Sales representative for further assistance and for arrangements of product return. The customers are being ask to return the enclosed "Recall Acknowledge and Return Form" indicating whether or not they possess any of the affected product identified. Integra will replace any product affected by this Recall that is returned. Please feel free to contact me at 609-936-5407 should you have any additional questions.
Details
- Recall number
- Z-1081-2010
- Initiated
- January 13, 2010
- Posted by FDA
- March 11, 2010
- Terminated
- March 18, 2010
- Product code
- GXQ – Dura Substitute
- Quantity
- 94
- Distribution
- Nationwide distribution:Ca, NY, TX, CO, VA, SC, IA, MO, IL, LA, OR, OH, WI, FL, DC, DE, MD, MN.
- Recalling firm
- Integra LifeSciences Corp, Plainsboro, NJ