Reported Feb 25, 2026 · Ongoing
Medline Convenience 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 Convenience Kits
74 of 74 products
| Model / number | Product as published |
|---|---|
CDS840015AQ | OPEN HEART CDS |
CDS840023T | OPEN HEART CDS |
CDS840087AI | OFF PUMP CABG CDS |
CDS840087AK | OFF PUMP CABG CDS |
CDS840087AL | OFF PUMP CABG CDS |
CDS840150S | OPEN HEART |
CDS840150T | OPEN HEART |
CDS840150U | OPEN HEART |
CDS840150V | OPEN HEART |
CDS840150W | OPEN HEART |
CDS840246O | UNIVERSAL HEART CDS |
CDS840261AB | GENERAL AAA #11-RF |
CDS840396AA | OPEN HEART ADULT |
CDS840396AB | OPEN HEART ADULT |
CDS840396X | OPEN HEART ADULT |
CDS840396Y | OPEN HEART ADULT |
CDS840428K | OPEN HEART CDS |
CDS840428L | OPEN HEART CDS |
CDS980839C | PACEMAKER CDS |
CDS982564C | KIT, CVC ADD A PACK HUM-LF |
- Lot codes and dates
359 of 359 products
Products covered by this recall # Barcodes Product as published 1 1019348968206940193489682060Lot Number: 23FLA191; 2) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 2 1019348968206940193489682060Lot Number: 23LBM199; 3) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 3 1019348968206940193489682060Lot Number: 23KBM369; 4) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 4 1019348968206940193489682060Lot Number: 23JBU616; 5) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 5 1019348968206940193489682060Lot Number: 23IBJ759; 6) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 6 1019348968206940193489682060Lot Number: 23IBJ571; 7) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 7 1019348968206940193489682060Lot Number: 23GBA105; 8) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 8 1019348968206940193489682060Lot Number: 23CBO830; 9) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 9 1019348968206940193489682060Lot Number: 23ABM709; 10) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 10 1019348968206940193489682060Lot Number: 23ABE738; 11) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 11 1019348968206940193489682060Lot Number: 22OBM690; 12) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 12 1019348968206940193489682060Lot Number: 22KBW565; 13) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 13 1019348968206940193489682060Lot Number: 22KBL256; 14) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 14 1019348968206940193489682060Lot Number: 22KBJ798; 15) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 15 1019348968206940193489682060Lot Number: 22JBU353; 16) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 16 1019348968206940193489682060Lot Number: 22JBT770; 17) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 17 1019348968206940193489682060Lot Number: 22HBU935; 18) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 18 1019348968206940193489682060Lot Number: 22GBQ917; 19) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 19 1019348968206940193489682060Lot Number: 22EBK678; 20) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) 20 1019348968206940193489682060Lot Number: 22CBC309; 21) CDS840023T, UDI-DI: 10193489682069(each), 40193489682060(case) - Amount recalled
- 39315 units
This recall covers 43 products
The agency filed one notice per product. You are reading one of them; the other 42 are below.
30 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
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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