Collagen Reagent, Cat. No. 5368, 2 X 1 mL, For use in platelet aggregation studies, Contains: Collagen (equine tendon) For In-Vitro Diagnostic Use,
FDA Recall Z-0537-2020 · Posted None
Recalling FirmHelena Laboratories, Corp.
Recall StatusOpen, Classified
Product CodeGHR
Date Initiated2018-05-23
Product Quantity64 Aggregation Kits
Reason for Recall
Through an investigation, it has been determined that vials of Collagen packaged within the Collagen Reagent and Platelet aggregation Kit, may contain particulate matter or microbial growth.
Firm Action
On 05/23/2018, the firm's technical services contacted consignees via phone call with a email follow-up of their recall notification letter. Consignees were advised of the following:
1. Prevent any shipment or schedule demonstrations with these lots
2. Remove the lots from available inventory and discard COLLAGEN vials.
3. Verify amount REMOVED FROM STOCK
4. COMPLETE THE FORM AND RETURN TO HELENA LABORATORIES, USA VIA: fax: 409-842-1874 OR E-MAIL TO [email protected]. For questions, contact Jessica W. Jones, MD, MPH - Mgr., Technical Services at: 1 (409) 842-3714 ext. 1177
Root Cause
Unknown/Undetermined by firm
Distribution Pattern
US:TX, WV, OH, TN, GA, TN, NY, ME, MA,LA, AZ OUS: Israel, Korea, Australia, Indonesia, Canada, Thailand, Colombia, Brasil , China , Taiwan
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.