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
7 of 7 products
| Model / number | Product as published |
|---|---|
DYNJ32841F | BWNBORO CRANIOTOMY PACK-LF |
DYNJ46069D | CRANIOTOMY PACK-LF |
DYNJ51935A | CAMPUS EXTREMITY PK |
DYNJ68902A | FOOT -XRAY BOWL MEDCUP SPECCUP |
DYNJ80679A | RADIOLOGY SPINE PACK |
DYNJ82370A | DR CHA CUSTOM PACK |
DYNJ84272 | SPINE PACK HC |
- Lot codes and dates
25 of 25 products
Products covered by this recall # Barcodes Product as published 1 1019348949318440193489493185Lot Number: 24CBF407; 2) DYNJ46069D, UDI-DI: 10193489493184(each), 40193489493185(case) 2 1088994273554940889942735540Lot Number: 24KBG704; 3) DYNJ51935A, UDI-DI: 10889942735549(each), 40889942735540(case) 3 1019348987041140193489870412Lot Number: 24BME364; 4) DYNJ68902A, UDI-DI: 10193489870411(each), 40193489870412(case) 4 1019532727370540195327273706Lot Number: 24BMC999; 5) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) 5 1019532727370540195327273706Lot Number: 22KBJ690; 6) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) 6 1019532727370540195327273706Lot Number: 23BBD696; 7) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) 7 1019532727370540195327273706Lot Number: 23DBG588; 8) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) 8 1019532727370540195327273706Lot Number: 23FBD221; 9) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) 9 1019532727370540195327273706Lot Number: 23GBN050; 10) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) 10 1019532727370540195327273706Lot Number: 23IBB710; 11) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) 11 1019532727370540195327273706Lot Number: 23LBM277; 12) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) 12 1019532727370540195327273706Lot Number: 24CBN011; 13) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) 13 1019532727370540195327273706Lot Number: 24DBK248; 14) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) 14 1019532727370540195327273706Lot Number: 24GBC694; 15) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) 15 1019532727370540195327273706Lot Number: 24HBX136; 16) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) 16 1019532727370540195327273706Lot Number: 24IBR538; 17) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) 17 1019532727370540195327273706Lot Number: 25ABC728; 18) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) 18 1019532727370540195327273706Lot Number: 25CBE147; 19) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) 19 1019532727370540195327273706Lot Number: 25CBP816; 20) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) 20 1019532727370540195327273706Lot Number: 23JBS196; 21) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case) - Amount recalled
- 2609 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.
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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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