Class II U.S. Food and Drug Administration

Medline medical convenience kits labeled recall: Reports of problems with product being difficult to remove from patient

Recall published 5 days ago

Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.

The hazard: Device safety concern

A device recall was filed for this product. For anything implanted or relied on daily, the clinician comes before the paperwork.

What the notice says: Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.

Why it matters: The FDA recorded an enforcement action against this device. Most device recalls are corrections rather than removals, so the device often stays in use while the manufacturer issues a fix.

Recall details

Recall number
Z-0275-2027
Published
October 28, 2026
Risk level
Class II
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
Medline Industries, LP
Product type
Medical devices
Units affected
26965 kits
Distribution
Nationwide
Made in
United States
Lot / code info
Medline Kit Number/SKU CDS980963D, UDI/DI 10889942942091 (each) 40889942942092 (case), Lot Number 26HBU410; Medline Kit Number/SKU CDS980963D, UDI/DI 10889942942091 (each) 40889942942092 (case), Lot Number 26GBU519; Medline Kit Number/SKU CDS983917O, UDI/DI 10195327583392 (each) 40195327583393 (case), Lot Number 26EBR697; Medline Kit Number/SKU CDS983917O, UDI/DI 10195327583392 (each) 40195327583393 (case), Lot Number 26DBS199; Medline Kit Number/SKU CDS983917O, UDI/DI 10195327583392 (each) 40195327583393 (case), Lot Number 26CBO921; Medline Kit Number/SKU CDS983917O, UDI/DI 10195327583392 (each) 40195327583393 (case), Lot Number 26CBF309; Medline Kit Number/SKU CDS983917O, UDI/DI 10195327583392 (each) 40195327583393 (case), Lot Number 25LBJ133; Medline Kit Number/SKU CDS983917O, UDI/DI 10195327583392 (each) 40195327583393 (case), Lot Number 25KBK360; Medline Kit Number/SKU CDS984264J, UDI/DI 10198459303142 (each) 40198459303143 (case), Lot Number 26FBM729; Medline Kit Number/SKU CDS984264J, UDI/DI 10198459303142 (each) 40198459303143 (case), Lot Number 25KBA584; Medline Kit Number/SKU DYNJT0473L, UDI/DI 10198459727924 (each) 40198459727925 (case), Lot Number 26EMH174; Medline Kit Number/SKU DYNJT10306, UDI/DI 10198459787232 (each) 40198459787233 (case), Lot Number 26FBD165; Medline Kit Number/SKU DYNJT2552G, UDI/DI 10198459334733 (each) 40198459334734 (case), Lot Number 26HMB198; Medline Kit Number/SKU DYNJT2552G, UDI/DI 10198459334733 (each) 40198459334734 (case), Lot Number 26EMJ491; Medline Kit Number/SKU DYNJT2552G, UDI/DI 10198459334733 (each) 40198459334734 (case), Lot Number 25LMF446; Medline Kit Number/SKU DYNJT2552G, UDI/DI 10198459334733 (each) 40198459334734 (case), Lot Number 25LMB213; Medline Kit Number/SKU DYNJT2552G, UDI/DI 10198459334733 (each) 40198459334734 (case), Lot Number 25JMK298; Medline Kit Number/SKU DYNJT3029, UDI/DI 10198459304026 (each) 40198459304027 (case), Lot Number 26CBU228; Medline Kit Number/SKU DYNJT3029, UDI/DI 10198459304026 (each) 40198459304027 (case), Lot Number 26BBK879; Medline Kit Number/SKU DYNJT3029, UDI/DI 10198459304026 (each) 40198459304027 (case), Lot Number 25LBB304; Medline Kit Number/SKU DYNJT3029, UDI/DI 10198459304026 (each) 40198459304027 (case), Lot Number 25KBD872; Medline Kit Number/SKU DYNJT3029, UDI/DI 10198459304026 (each) 40198459304027 (case), Lot Number 25JBT106; Medline Kit Number/SKU DYNJT3029A, UDI/DI 10198459767005 (each) 40198459767006 (case), Lot Number 26GBB911; Medline Kit Number/SKU DYNJT3029A, UDI/DI 10198459767005 (each) 40198459767006 (case), Lot Number 26FBA224; Medline Kit Number/SKU DYNJT3886, UDI/DI 10198459366864 (each) 40198459366865 (case), Lot Number 26GBY667; Medline Kit Number/SKU DYNJT3886, UDI/DI 10198459366864 (each) 40198459366865 (case), Lot Number 26FBR365; Medline Kit Number/SKU DYNJT3886, UDI/DI 10198459366864 (each) 40198459366865 (case), Lot Number 26FBC178; Medline Kit Number/SKU DYNJT3886, UDI/DI 10198459366864 (each) 40198459366865 (case), Lot Number 26EBA314; Medline Kit Number/SKU DYNJT3886, UDI/DI 10198459366864 (each) 40198459366865 (case), Lot Number 26CBL921; Medline Kit Number/SKU DYNJT3886, UDI/DI 10198459366864 (each) 40198459366865 (case), Lot Number 26BBG767; Medline Kit Number/SKU DYNJT3886, UDI/DI 10198459366864 (each) 40198459366865 (case), Lot Number 26ABM195; Medline Kit Number/SKU DYNJT3886, UDI/DI 10198459366864 (each) 40198459366865 (case), Lot Number 25LBU705; Medline Kit Number/SKU DYNJT3936, UDI/DI 10198459378461 (each) 40198459378462 (case), Lot Number 26FBQ657; Medline Kit Number/SKU DYNJT3936, UDI/DI 10198459378461 (each) 40198459378462 (case), Lot Number 26FBN614; Medline Kit Number/SKU DYNJT3936, UDI/DI 10198459378461 (each) 40198459378462 (case), Lot Number 26EBC371; Medline Kit Number/SKU DYNJT3936, UDI/DI 10198459378461 (each) 40198459378462 (case), Lot Number 26BBK901; Medline Kit Number/SKU DYNJT4106, UDI/DI 10198459401398 (each) 40198459401399 (case), Lot Number 26CMH903; Medline Kit Number/SK…
UPC codes
10889942942091, 40889942942092, 10195327583392, 40195327583393, 10198459303142, 40198459303143, 10198459727924, 40198459727925, 10198459787232, 40198459787233, 10198459334733, 40198459334734, 10198459304026, 40198459304027, 10198459767005, 40198459767006, 10198459366864, 40198459366865, 10198459378461, 40198459378462

Products covered by this recall

MEDLINE medical convenience kits labeled as (list truncated)

Check your product

The notice names 61 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

UPC / barcode

Read the twelve digits under the barcode on the package.

  • 10889942942091
  • 40889942942092
  • 10195327583392
  • 40195327583393
  • 10198459303142
  • 40198459303143
  • 10198459727924
  • 40198459727925
  • 10198459787232
  • 40198459787233
  • 10198459334733
  • 40198459334734
  • 10198459304026
  • 40198459304027
  • 10198459767005
  • 40198459767006
  • 10198459366864
  • 40198459366865
  • 10198459378461
  • 40198459378462

Lot or batch code

Usually ink-stamped near the seam, the cap or the bottom of the pack.

  • 26HBU410
  • 26GBU519
  • 26EBR697
  • 26DBS199
  • 26CBO921
  • 26CBF309
  • 25LBJ133
  • 25KBK360
  • 26FBM729
  • 25KBA584
  • 26EMH174
  • 26FBD165
  • 26HMB198
  • 26EMJ491
  • 25LMF446
  • 25LMB213
  • 25JMK298
  • 26CBU228
  • 26BBK879
  • 25LBB304

Model or item number

On the rating label, the box or the instruction sheet.

  • CDS980963D
  • UDI/DI 10889942942091
  • CDS983917O
  • UDI/DI 10195327583392
  • CDS984264J
  • UDI/DI 10198459303142
  • DYNJT0473L
  • UDI/DI 10198459727924
  • DYNJT10306
  • UDI/DI 10198459787232
  • DYNJT2552G
  • UDI/DI 10198459334733
  • DYNJT3029
  • UDI/DI 10198459304026
  • DYNJT3029A
  • UDI/DI 10198459767005
  • DYNJT3886
  • UDI/DI 10198459366864
  • DYNJT3936
  • UDI/DI 10198459378461

Package size

Match the net weight or the piece count on the front of the pack.

  • 0473 L

Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Device

Medline Industries, LP — A device recall was filed for this product. For anything implanted or relied on daily, the clinician comes before the paperwork.

  1. Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.
  2. If you are a facility, quarantine affected stock and log the correction.
  3. Report device problems to the FDA through MedWatch.
  4. If the device is implanted or you depend on it daily, speak to your clinician before changing how you use it.

Claiming on a recalled device

Device recalls are tracked by serial and lot number, so your claim moves faster if you lead with those.

  • Have the model, catalogue, lot and serial numbers ready before you call — they are on the device label or its box.
  • Ask explicitly whether your unit is in the affected range; many recalls cover only part of a model line.
  • If you need the device daily, ask what interim arrangement they offer while the remedy is carried out.
  • Log the date, the name and the reference number of every call. Device recalls can run for months.

Company contact: Medline Industries, LP — 3 Lakes Dr, Northfield, IL, 60093-2753

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was Medline Industries, LP medical devices recalled?

Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 10889942942091, 40889942942092, 10195327583392; lot code 26HBU410, 26GBU519, 26EBR697; model number CDS980963D, UDI/DI 10889942942091, CDS983917O. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.

Can I get my money back?

Have the model, catalogue, lot and serial numbers ready before you call — they are on the device label or its box.

Where was the recalled product sold?

It was distributed nationwide.

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