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FDA (Device enforcement)Recalled 2025-03-03class ii

MEDLINE INDUSTRIES, LP - Northfield: Medline Convenience kits used for various procedures: 1) UTHET TYLER OB PACK, Model Number: DYNJ68673; 2) D AND C PACK, Model Number: DYNJ66290A; 3) D & C PACK-LF,

Hazard

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Details from the source

Reason for recall: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits. Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands. Quantity: 2,531 units Lot/code info: 1) DYNJ68673, UDI-DI: 10193489839951(each), 40193489839952(case), Lot Number: 24IBG873; 2) DYNJ66290A, UDI-DI: 10193489461428(each), 40193489461429(case), Lot Number: 24IBG957; 3) DYNJ24159C, UDI-DI: 10198459032394(each), 40198459032395(case), Lot Number: 24IBL229; 4) DYNJ54484A, UDI-DI: 10193489813074(each), 40193489813075(case), Lot Number: 24IBS805; 5) DYNJS3040, UDI-DI: 10884389602225(each), 40884389602226(case), Lot Number: 24JBL655; 6) DYNJ900422F, UDI-DI: 10195327658373(each), 40195327658374(case), Lot Number: 24JBM234; 7) CDS985201A, UDI-DI: 10889942942312(each), 40889942942313(case), Lot Number: 24JBN479; 8) DYNJ66290A, UDI-DI: 10193489461428(each), 40193489461429(case), Lot Number: 24JBN645; 9) DYNJ47616B, UDI-DI: 10193489731040(each), 40193489731041(case), Lot Number: 24JBT461; 10) DYNJ50656B, UDI-DI: 10195327306410(each), 40195327306411(case), Lot Number: 24JBT906; 11) DYNJ36599, UDI-DI: 10884389554142(each), 40884389554143(case), Lot Number: 24JBW173; 12) DYNJ25915G, UDI-DI: 10193489718942(each), 40193489718943(case), Lot Number: 24JBW203; 13) DYNJS3040, UDI-DI: 10884389602225(each), 40884389602226(case), Lot Number: 24JBW545; 14) DYNJ0989660A, UDI-DI: 10889942136131(each), 40889942136132(case), Lot Number: 24JBX677; 15) DYNJ64226A, UDI-DI: 10195327135430(each), 40195327135431(case), Lot Number: 24KBC728; 16) DYNJ64571, UDI-DI: 10193489208986(each), 40193489208987(case), Lot Number: 24KBD692; 17) DYNJ50656B, UDI-DI: 10195327306410(each), 40195327306411(case), Lot

UPC codes

10193489839951, 40193489839952, 10193489461428, 40193489461429, 10198459032394, 40198459032395, 10193489813074, 40193489813075, 10884389602225, 40884389602226, 10195327658373, 40195327658374, 10889942942312, 40889942942313, 10193489731040, 40193489731041, 10195327306410, 40195327306411, 10884389554142, 40884389554143, 10193489718942, 40193489718943, 10889942136131, 40889942136132, 10195327135430, 40195327135431, 10193489208986, 40193489208987, 10195327548506, 40195327548507, 10193489691511, 40193489691512, 10889942225248, 40889942225249, 10193489247244, 40193489247245

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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