Reported Apr 23, 2025 · Ongoing
Medline Convenience kits used for various procedures
MEDLINE INDUSTRIES, LP - Northfield
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: MEDLINE INDUSTRIES, LP - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
Medline Convenience kits used for various procedures
16 of 16 products
| Model / number | Product as published |
|---|---|
DYNJ44949C | LINE INSERTION PACK |
DYNJ41682C | PICC LINE INSERTION BJC-LF |
DYNJ81267A | SUPERFICIAL VENOUS PROCEDURE |
DYNJ82437A | ILR INSERTION-REMOVAL PACK |
CDS980379J | C LINE INSERTION CDS |
DYNJ24529M | BSHR PICC LINE-LF |
DYNJ65827 | ENSEMBLE POWER PICC-HEJ-LF |
DYNJ55170F | PICC LINE PACK |
DYNJ44949C | LINE INSERTION PACK |
DYNJ67899A | RFA PACK |
PHS902533005 | KIT CENTRAL LINE INSERTION-LF |
DYNDH1904 | INFANT LUMBAR PUNCTURE TRAY |
DYNJ55356A | PICC PACK-LF |
DYNJ15652M | GENERAL TRAY |
DYNJ80643 | CVR ENDOVENOUS PACK |
DYNJ20803D | LINE INSERTION TRAY |
- Lot codes and dates
16 of 16 products
Products covered by this recall # Barcodes Product as published 1 1019845908551240198459085513Lot Number: 24IBS279; 2) DYNJ41682C, UDI-DI: 10198459085512(each), 40198459085513(case) 2 1019532735235640195327352357Lot Number: 24JBM452; 3) DYNJ81267A, UDI-DI: 10195327352356(each), 40195327352357(case) 3 1019845911100640198459111007Lot Number: 24JBO094; 4) DYNJ82437A, UDI-DI: 10198459111006(each), 40198459111007(case) 4 1019532705490840195327054909Lot Number: 24JBT077; 5) CDS980379J, UDI-DI: 10195327054908(each), 40195327054909(case) 5 1019348967828440193489678285Lot Number: 24JBT886; 6) DYNJ24529M, UDI-DI: 10193489678284(each), 40193489678285(case) 6 1019348929849940193489298490Lot Number: 24JBT947; 7) DYNJ65827, UDI-DI: 10193489298499(each), 40193489298490(case) 7 1019532761465240195327614653Lot Number: 24JBW632; 8) DYNJ55170F, UDI-DI: 10195327614652(each), 40195327614653(case) 8 1019348976922740193489769228Lot Number: 24KBB128; 9) DYNJ44949C, UDI-DI: 10193489769227(each), 40193489769228(case) 9 1019845907148540198459071486Lot Number: 24KBB902; 10) DYNJ67899A, UDI-DI: 10198459071485(each), 40198459071486(case) 10 1088994204392740889942043928Lot Number: 24KBC476; 11) PHS902533005, UDI-DI: 10889942043927(each), 40889942043928(case) 11 1019532746377940195327463770Lot Number: 24KBD388; 12) DYNDH1904, UDI-DI: 10195327463779(each), 40195327463770(case) 12 1019348964619140193489646192Lot Number: 24KBD507; 13) DYNJ55356A, UDI-DI: 10193489646191(each), 40193489646192(case) 13 1019845916941040198459169411Lot Number: 24KBE301; 14) DYNJ15652M, UDI-DI: 10198459169410(each), 40198459169411(case) 14 1019532705579040195327055791Lot Number: 24KBE666; 15) DYNJ80643, UDI-DI: 10195327055790(each), 40195327055791(case) 15 1088994255388440889942553885Lot Number: 24KBH524; 16) DYNJ20803D, UDI-DI: 10889942553884(each), 40889942553885(case) 16 Lot Number: 24KBJ200 - Amount recalled
- 3808 units
This recall covers 34 products
The agency filed one notice per product. You are reading one of them; the other 33 are below.
21 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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