Medline medical procedure kits labeled as follows: DENTAL, REF DYNJ909211A
FDA Recall Z-2702-2024 · Posted 2024-08-22
Recalling FirmMEDLINE INDUSTRIES, LP - Northfield
Recall StatusOpen, Classified
Product CodeOFX
Date Initiated2024-03-22
Product Quantity99 units
Reason for Recall
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Firm Action
Medline Industries issued a Safety Alert to its consignees on 03/22/2024 via email and certified mail. The notice explained the problem with the device and requested that consignees follow the instructions for use. Distributors or those who further transferred the affected product were directed to notify their consignees.
Root Cause
Under Investigation by firm
Distribution Pattern
Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.