Medline Convenience kits used for various procedures: 1) LINE INSERTION PACK, Model Number: DYNJ44949C; 2) PICC LINE ... — FDA record Z-1593-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Mar 3, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Medline Convenience kits used for various procedures: 1) LINE INSERTION PACK, Model Number: DYNJ44949C; 2) PICC LINE INSERTION BJC-LF, Model Number: DYNJ41682C; 3) SUPERFICIAL VENOUS PROCEDURE, Model Number: DYNJ81267A; 4) ILR INSERTION-REMOVAL PACK, Model Number: DYNJ82437A; 5) C LINE INSERTION CDS, Model Number: CDS980379J; 6) BSHR PICC LINE-LF, Model Number: DYNJ24529M; 7) ENSEMBLE POWER PICC-HEJ-LF, Model Number: DYNJ65827; 8) PICC LINE PACK, Model Number: DYNJ55170F; 9) LINE INSERTION PACK, Model Number: DYNJ44949C; 10) RFA PACK, Model Number: DYNJ67899A; 11) KIT CENTRAL LINE INSERTION-LF, Model Number: PHS902533005; 12) INFANT LUMBAR PUNCTURE TRAY, Model Number: DYNDH1904; 13) PICC PACK-LF, Model Number: DYNJ55356A; 14) GENERAL TRAY, Model Number: DYNJ15652M; 15) CVR ENDOVENOUS PACK, Model Number: DYNJ80643; 16) LINE INSERTION TRAY, Model Number: DYNJ20803D
Reason
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Classification
Class II
Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Quantity
3808 units
Agency-reported status
Ongoing
Source record identifier
Z-1593-2025

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicability1) DYNJ44949C, UDI-DI: 10193489769227(each), 40193489769228(case), Lot Number: 24IBS279; 2) DYNJ41682C, UDI-DI: 10198459085512(each), 40198459085513(case), Lot Number: 24JBM452; 3) DYNJ81267A, UDI-DI: 10195327352356(each), 40195327352357(case), Lot Number: 24JBO094; 4) DYNJ82437A, UDI-DI: 10198459111006(each), 40198459111007(case), Lot Number: 24JBT077; 5) CDS980379J, UDI-DI: 10195327054908(each), 40195327054909(case), Lot Number: 24JBT886; 6) DYNJ24529M, UDI-DI: 10193489678284(each), 40193489678285(case), Lot Number: 24JBT947; 7) DYNJ65827, UDI-DI: 10193489298499(each), 40193489298490(case), Lot Number: 24JBW632; 8) DYNJ55170F, UDI-DI: 10195327614652(each), 40195327614653(case), Lot Number: 24KBB128; 9) DYNJ44949C, UDI-DI: 10193489769227(each), 40193489769228(case), Lot Number: 24KBB902; 10) DYNJ67899A, UDI-DI: 10198459071485(each), 40198459071486(case), Lot Number: 24KBC476; 11) PHS902533005, UDI-DI: 10889942043927(each), 40889942043928(case), Lot Number: 24KBD388; 12) DYNDH1904, UDI-DI: 10195327463779(each), 40195327463770(case), Lot Number: 24KBD507; 13) DYNJ55356A, UDI-DI: 10193489646191(each), 40193489646192(case), Lot Number: 24KBE301; 14) DYNJ15652M, UDI-DI: 10198459169410(each), 40198459169411(case), Lot Number: 24KBE666; 15) DYNJ80643, UDI-DI: 10195327055790(each), 40195327055791(case), Lot Number: 24KBH524; 16) DYNJ20803D, UDI-DI: 10889942553884(each), 40889942553885(case), Lot Number: 24KBJ200

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Apr 23, 2025
Recall initiation date
Mar 3, 2025
Center classification date
Apr 17, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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