Reported Apr 29, 2026 · Ongoing
Medline Kits
Medline Industries, LP
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 · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
Medline Kits
65 of 65 products
| Model / number | Product as published |
|---|---|
60021775 | MTS LEFT HEART KIT-CAROLINAS HOS |
60022026 | DBD-MTS LHK BHS BAPTIST. LOUISVI |
60022673 | MTO LEFT HEART KIT SUMMA BARBERT |
60030817 | MTS LH KIT-UNIV OF MIAMI PG |
60031245 | MTS LEFT HEART KIT SPRINGFIELD R |
60031247 | MTS PERIPHERAL KIT SPRINGFIELD R |
60031928 | MTS LEFT HEART KIT-COLISEUM MED |
60033011 | MTS LEFT HEART KIT -2-CALIFORNIA |
60040273 | MTS LEFT HEART KIT JOHN MUIR CON |
60041268 | MTS EP MANIFOLD KIT TEXAS HLTH P |
60050097 | MTS 3V MANIFOLD KIT-SPARROW HOSP |
60060387 | MTS LEFT HEART KIT FORT SANDERS |
60070435 | MTS LEFT HEART KIT-GOOD SAMARITA |
60070521 | DBD-MTS ANGIO KIT-MOUNT HOOD MED |
60071743 | MTS LFT HRT KIT-GRAND VIEW PG |
60090078 | MTS CUSTOM MANIFOLD KIT-INGALLS |
60090542 | MTS CATH LAB KIT - HEARTLAND PG |
60100071 | MTS LEFT HEART KIT-W.C.A PG |
60100254 | MTS MANIFOLD KIT-GENESYS REG MED |
60100439 | MTS 4V W/PRO STA-ST.JOHNS REG ME |
- Lot codes and dates
152 of 152 products
Products covered by this recall # Barcodes Product as published 1 1019348904138520193489041382Lot Number: 183372; 2) 60021775, UDI-DI: 10193489041385(each), 20193489041382(case) 2 1019348908725320193489087250Lot Number: 185190; 3) 60022026, UDI-DI: 10193489087253(each), 20193489087250(case) 3 1019348908725320193489087250Lot Number: 106008; 4) 60022026, UDI-DI: 10193489087253(each), 20193489087250(case) 4 1019348904153820193489041535Lot Number: 117378; 5) 60022673, UDI-DI: 10193489041538(each), 20193489041535(case) 5 1019348904197220193489041979Lot Number: 176180; 6) 60030817, UDI-DI: 10193489041972(each), 20193489041979(case) 6 1019348904221420193489042211Lot Number: 185193; 7) 60031245, UDI-DI: 10193489042214(each), 20193489042211(case) 7 1019348904223820193489042235Lot Number: 183374; 8) 60031247, UDI-DI: 10193489042238(each), 20193489042235(case) 8 1019348904223820193489042235Lot Number: 174370; 9) 60031247, UDI-DI: 10193489042238(each), 20193489042235(case) 9 1019348904223820193489042235Lot Number: 184424; 10) 60031247, UDI-DI: 10193489042238(each), 20193489042235(case) 10 1019348904227620193489042273Lot Number: 185080; 11) 60031928, UDI-DI: 10193489042276(each), 20193489042273(case) 11 1019348904242920193489042426Lot Number: 185195; 12) 60033011, UDI-DI: 10193489042429(each), 20193489042426(case) 12 1019348904283220193489042839Lot Number: 181365; 13) 60040273, UDI-DI: 10193489042832(each), 20193489042839(case) 13 1019348904283220193489042839Lot Number: 179872; 14) 60040273, UDI-DI: 10193489042832(each), 20193489042839(case) 14 1019348904305120193489043058Lot Number: 183375; 15) 60041268, UDI-DI: 10193489043051(each), 20193489043058(case) 15 1019348904305120193489043058Lot Number: 140365; 16) 60041268, UDI-DI: 10193489043051(each), 20193489043058(case) 16 1019348904324220193489043249Lot Number: 170084; 17) 60050097, UDI-DI: 10193489043242(each), 20193489043249(case) 17 1019348904369320193489043690Lot Number: 176186; 18) 60060387, UDI-DI: 10193489043693(each), 20193489043690(case) 18 1019348904369320193489043690Lot Number: 183376; 19) 60060387, UDI-DI: 10193489043693(each), 20193489043690(case) 19 1019348904369320193489043690Lot Number: 185194; 20) 60060387, UDI-DI: 10193489043693(each), 20193489043690(case) 20 1019348904413320193489044130Lot Number: 187370; 21) 60070435, UDI-DI: 10193489044133(each), 20193489044130(case) - Amount recalled
- 19189 units
This recall covers 39 products
The agency filed one notice per product. You are reading one of them; the other 38 are below.
26 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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