Reported Oct 30, 2024 · Ongoing

Medline brand medical procedure convenience kits, labeled as

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?

142 of 142 products

Products covered by this recall
Model / numberBarcodesProduct as published
00-400616J4019348959224610193489592245UDI/DI 40193489592246 (each), 10193489592245 (case), Lot Numbers: 24ABI725
3706WHST4019348944570210193489445701UDI/DI 40193489445702 (each), 10193489445701 (case), Lot Numbers: 24ABG100
CDS980427J4088994282357510889942823574UDI/DI 40889942823575 (each), 10889942823574 (case), Lot Numbers: 24DBG751
CDS9846034088438985378910884389853788UDI/DI 40884389853789 (each), 10884389853788 (case), Lot Numbers: 24BBB784
CHT7454065316026365510653160263654UDI/DI 40653160263655 (each), 10653160263654 (case), Lot Numbers: 23LBM800
DYND150814TS4019532714970410195327149703UDI/DI 40195327149704 (each), 10195327149703 (case), Lot Numbers: 23KBD258
DYND150814TS4019532714970410195327149703UDI/DI 40195327149704 (each), 10195327149703 (case), Lot Numbers: 23KBA940
DYNDA20604088994269733610889942697335UDI/DI 40889942697336 (each), 10889942697335 (case), Lot Numbers: 24ABN606
DYNDA22034088994281377410889942813773UDI/DI 40889942813774 (each), 10889942813773 (case), Lot Numbers: 24ABD615
DYNDA29144019532709280210195327092801UDI/DI 40195327092802 (each), 10195327092801 (case), Lot Numbers: 23LBL366
DYNDH17654019532720576910195327205768UDI/DI 40195327205769 (each), 10195327205768 (case), Lot Numbers: 24ABG092
DYNJ00017M4019532749203910195327492038UDI/DI 40195327492039 (each), 10195327492038 (case), Lot Numbers: 24ABD093
DYNJ0259819I4019348997290110193489972900UDI/DI 40193489972901 (each), 10193489972900 (case), Lot Numbers: 24ABB267
DYNJ0259819I4019348997290110193489972900UDI/DI 40193489972901 (each), 10193489972900 (case), Lot Numbers: 23KBO771
DYNJ0259819I4019348997290110193489972900UDI/DI 40193489972901 (each), 10193489972900 (case), Lot Numbers: 23JBS007
DYNJ0410060S4019532744089410195327440893UDI/DI 40195327440894 (each), 10195327440893 (case), Lot Numbers: 23LBR879
DYNJ14063D4088438987361910884389873618UDI/DI 40884389873619 (each), 10884389873618 (case), Lot Numbers: 24ABF481
DYNJ14063D4088438987361910884389873618UDI/DI 40884389873619 (each), 10884389873618 (case), Lot Numbers: 23LBN035
DYNJ17310D4019348977540310193489775402UDI/DI 40193489775403 (each), 10193489775402 (case), Lot Numbers: 23LBK791
DYNJ21241D4088438983887810884389838877UDI/DI 40884389838878 (each), 10884389838877 (case), Lot Numbers: 23LBL798
Amount recalled
22,327 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

XXX

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:35 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.