Reported May 13, 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
26 of 26 products
| Model / number | Product as published |
|---|---|
00-401993O | PICC LINE TRAY |
ACC010268B | CODE CART ADULT 4 CENTRAL LINE |
ACC010268C | CODE CART ADULT 4 CENTRAL LINE |
ACC010487 | TRAY 6 CENTRAL LINE A |
CVI3650 | PEDS PICC INSERTION TRAY |
DYKM2170 | LINE ATTIRE KIT |
DYKM2274 | PK BNDL CENT LINE PROTECT KIT |
DYKMBNDL153C | KIT SURG ONC LAP DIAG/PORT INS |
DYKMBNDL43A | KIT SURG ONC INSERT CENT.VENOU |
DYKMBNDL43C | KIT SURG ONC PORT INSERTION |
DYNDA2076B | VEIN PROCEDURE KIT |
DYNDA2076D | VEIN PROCEDURE KIT |
DYNDA2076F | VEIN PROCEDURE KIT |
DYNDA2322B | PLACENTA KIT |
DYNDC2407A | NICU CENTRAL LINE TRAY |
DYNDC2407B | NICU CENTRAL LINE TRAY |
DYNJ40500A | PICC LINE TRAY |
DYNJ42694C | VENOUS ACCESS PACK |
DYNJ53427B | AV FISTULA CREATION PACK-LF |
DYNJ55546D | PICC LINE |
- Lot codes and dates
96 of 96 products
Products covered by this recall # Barcodes Product as published 1 1088994219747740889942197478Lot Number: 23KBH528; 2) ACC010268B, UDI-DI: 10889942197477(each), 40889942197478(case) 2 1088994219747740889942197478Lot Number: 21BDB379; 3) ACC010268B, UDI-DI: 10889942197477(each), 40889942197478(case) 3 1088994219747740889942197478Lot Number: 21CDB078; 4) ACC010268B, UDI-DI: 10889942197477(each), 40889942197478(case) 4 1088994219747740889942197478Lot Number: 21IDC222; 5) ACC010268B, UDI-DI: 10889942197477(each), 40889942197478(case) 5 1088994219747740889942197478Lot Number: 21JDB458; 6) ACC010268B, UDI-DI: 10889942197477(each), 40889942197478(case) 6 1088994219747740889942197478Lot Number: 22ADC105; 7) ACC010268B, UDI-DI: 10889942197477(each), 40889942197478(case) 7 1088994219747740889942197478Lot Number: 22BDA862; 8) ACC010268B, UDI-DI: 10889942197477(each), 40889942197478(case) 8 1088994219747740889942197478Lot Number: 22CDC433; 9) ACC010268B, UDI-DI: 10889942197477(each), 40889942197478(case) 9 1088994219747740889942197478Lot Number: 22DDA763; 10) ACC010268B, UDI-DI: 10889942197477(each), 40889942197478(case) 10 1088994219747740889942197478Lot Number: 22FDB218; 11) ACC010268B, UDI-DI: 10889942197477(each), 40889942197478(case) 11 1088994219747740889942197478Lot Number: 23BDB271; 12) ACC010268B, UDI-DI: 10889942197477(each), 40889942197478(case) 12 1088994219747740889942197478Lot Number: 23DDA455; 13) ACC010268B, UDI-DI: 10889942197477(each), 40889942197478(case) 13 1088994219747740889942197478Lot Number: 23DDB175; 14) ACC010268B, UDI-DI: 10889942197477(each), 40889942197478(case) 14 1088994219747740889942197478Lot Number: 23FDC048; 15) ACC010268B, UDI-DI: 10889942197477(each), 40889942197478(case) 15 1088994219747740889942197478Lot Number: 23GDB567; 16) ACC010268B, UDI-DI: 10889942197477(each), 40889942197478(case) 16 1088994219747740889942197478Lot Number: 23IDA297; 17) ACC010268B, UDI-DI: 10889942197477(each), 40889942197478(case) 17 1019845901897840198459018979Lot Number: 24DDA188; 18) ACC010268C, UDI-DI: 10198459018978(each), 40198459018979(case) 18 1019845901897840198459018979Lot Number: 24HDB961; 19) ACC010268C, UDI-DI: 10198459018978(each), 40198459018979(case) 19 1019845901897840198459018979Lot Number: 24IDB060; 20) ACC010268C, UDI-DI: 10198459018978(each), 40198459018979(case) 20 1019845901897840198459018979Lot Number: 24JDB298; 21) ACC010268C, UDI-DI: 10198459018978(each), 40198459018979(case) - Amount recalled
- 5562 units
This recall covers 42 products
The agency filed one notice per product. You are reading one of them; the other 41 are below.
29 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.
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.
Free recall alerts
Get alerted about new Medline Industries, LP recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.