FDA Recall Terminated

Nylon Surgical Suture for human use and vet use, sold under brand name Riverlon, Securolon, Weblon. Product is sterile. Part numbers: 663BK 663BL 664BL 928BK Product Usage: For use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurological surgery.

Recall: Z-2761-2016 · Initiated August 5, 2016

Recall

Recall Number
Z-2761-2016
Event Number
74891
Firm
Riverpoint Medical, LLC
FEI Number
3006981798
Product Code
GAR
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
August 5, 2016
Terminated
December 22, 2016
Address
825 NE 25th Ave, Portland, OR, 97232-2304

Description

Nylon Surgical Suture for human use and vet use, sold under brand name Riverlon, Securolon, Weblon. Product is sterile. Part numbers: 663BK 663BL 664BL 928BK Product Usage: For use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurological surgery.

Reason

Nylon Surgical Sutures are recalled because the seals may become open during distribution or subsequent packaging.

Action

Riverpoint Medical sent an Urgent Medical Device letter, dated August 5. 2016, and the Customer Response Form to their customers via email. The letter identified the affected product, problem and actions to be taken. Customers are instructed to check inventory, discontinue selling affected sutures and return affected devices to the firm. Distributors are instructed to notify their downstream customers. Consignees should submit the Customer Response Forms. For questions call Riverpoint Medical at 1-866-445-4929.

Distribution

US Nationwide distribution in the states of ID, MA, OR, NY and in the country of Australia.

Quantity

2110 boxes distributed in the US and 72 boxes distributed outside US