ClearanceBrief
Recall Z-2714-2024 ยท OJH Orthopedic Tray

MEDLINE INDUSTRIES, LP - Northfield

Medline medical procedure kits labeled as follows: a) ARTHROSCOPY, REF DYNJ909699; b) BACK CDS, REF CDS984000C; c) EXTREMITY, REF DYNJ900847A; d) HAND-LF, REF DYNJ902619G; e) HIP PINNING CDS, REF CDS984009C; f) HIP PINNING/TFN/ANTERIOR HIP, REF DYNJ902380K; g) KNEE, REF DYNJ904771B; h) KNEE ARTHROSCOPY, REF DYNJ905519D; i) KNEE ARTHROSCOPY, REF DYNJ906273F; j) KNEE ARTHROSCOPY, REF DYNJ

DateAug 22, 2024 (initiated Mar 22, 2024)
StatusOpen, Classified
ReasonA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Root causeUnder Investigation by firm
ActionMedline 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.
Quantity14977 units
DistributionWorldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.