ClearanceBrief
Recall Z-0177-2025 ยท OKV Obstetrical Kit

MEDLINE INDUSTRIES, LP - Northfield

Medline brand medical procedure convenience kits, labeled as: a) OB PACK-LF, REF DYNJ0912449M; b) OB PACK, REF DYNJ17309G; c) OB PK, REF DYNJ34268D; d) OB DELIVERY PACK, REF DYNJ34274B; e) OB DELIVERY PACK, REF DYNJ34274B; f) D AND C PACK, REF DYNJ39668I; g) OB PACK, REF DYNJ42884; h) RFT D & C PACK, REF DYNJ50851; i) KIT OB, REF DYNJ906623; j) D AND C, REF DYNJ907957A; k) CHS OB PACK

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.
Quantity1506 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.