ClearanceBrief
Recall Z-0160-2025 ยท OGR Ear, Nose, And Throat Surgical Tray

MEDLINE INDUSTRIES, LP - Northfield

Medline brand medical procedure convenience kits, labeled as: 1) T&A CDS-LF, REF CDS982091I; 2) TONSIL CDS, REF CDS984492B; 3) RV T&A PACK-LF, REF DYNJ0798129I; 4) DIRECT MICRO LARYNG PK-LF, REF DYNJ30591I; 5) APU LINE PACK, REF DYNJ37171A; 6) T&A PACK-LF, REF DYNJ40836F; 7) ENT PACK, REF DYNJ44249J; 8) TONSIL PACK, REF DYNJ44349L; 9) TONSIL PACK, REF DYNJ44349M; 10) NASAL PACK, REF DYN

DateOct 23, 2024 (initiated Sep 4, 2024)
StatusOpen, Classified
ReasonIt has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
Root causeUnder Investigation by firm
ActionMedline issued a MEDICAL DEVICE RECALL notice to its consignees on 09/05/2024 via email and USPS. The notice explained the issue, hazard, and requested the destruction of the affected product. Distributors were directed to notify their consignees.
Quantity2740 units
DistributionWorldwide distribution - US Nationwide and the countries of Canada, Panama.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.