Reported Jan 8, 2025 · Ongoing

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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?

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Lot codes and dates

155 of 155 products

Products covered by this recall
Model / numberBarcodesProduct as published
CDS981185B1088438964714140884389647142UDI/DI 10884389647141 (EA) 40884389647142 (CS), Lot Numbers: 19CDB151, 19DDD096, 19FDA612, 19IDA540, 19LDB150, 20BDA647, 20DDB481, 20IDA733, 20LDA459
CDS983087G1019348923735140193489237352UDI/DI 10193489237351 (EA) 40193489237352 (CS), Lot Numbers: 21LBS976
CDS983302G1088827775318140888277753182UDI/DI 10888277753181 (EA) 40888277753182 (CS), Lot Numbers: 19JDB741
CDS983302I1019348942565940193489425650UDI/DI 10193489425659 (EA) 40193489425650 (CS), Lot Numbers: 23FDA273, 23IDA781
CDS983483G1088994294606840889942946069UDI/DI 10889942946068 (EA) 40889942946069 (CS), Lot Numbers: 19CDB914, 19DDB938, 19GDB412, 19GDC427, 19JDA647, 19KDB084, 19LDC222, 20BDC250, 20EDB879, 20GDC001, 20JDA007, 20JDB542, 20LDB199
CDS983483I1019348991958540193489919586UDI/DI 10193489919585 (EA) 40193489919586 (CS), Lot Numbers: 21FDB817, 21HDA571, 21KDB608, 22BDA109
CDS984313G1019348954043740193489540438UDI/DI 10193489540437 (EA) 40193489540438 (CS), Lot Numbers: 19GBL203, 20EBC321, 20KBB606
DYNJ0101278F1019348935235140193489352352UDI/DI 10193489352351 (EA) 40193489352352 (CS), Lot Numbers: 20FDA999, 20HDA734, 20KDB838, 21ADC024, 21CDA355, 21EDA527, 21GDC529, 21IDA040, 21IDA786, 21JDB214, 21KDC443, 22ADC117, 22CDB133
DYNJ0826316K1088994209264240889942092643UDI/DI 10889942092642 (EA) 40889942092643 (CS), Lot Numbers: 19FKB533, 19EKD537
DYNJ0826316L1019348941349640193489413497UDI/DI 10193489413496 (EA) 40193489413497 (CS), Lot Numbers: 21IME029, 21IMC729, 20IKB206
DYNJ0867411F1088994262057940889942620570UDI/DI 10889942620579 (EA) 40889942620570 (CS), Lot Numbers: 19EDA018
DYNJ10130D1019348943217640193489432177UDI/DI 10193489432176 (EA) 40193489432177 (CS), Lot Numbers: 21BBC490, 21GBS164, 22BBE642
DYNJ36728B1088994238920940889942389200UDI/DI 10889942389209 (EA) 40889942389200 (CS), Lot Numbers: 19BBG860, 19DBL861, 19HBF653, 19KBY296
DYNJ37254F1088994245012140889942450122UDI/DI 10889942450121 (EA) 40889942450122 (CS), Lot Numbers: 19BBG398, 19DBH566, 19GBJ891, 19IBU877, 19LBQ548, 20BBO050
DYNJ37254G1019348931779440193489317795UDI/DI 10193489317794 (EA) 40193489317795 (CS), Lot Numbers: 20DBV689, 20EBP226, 20LBT897, 20LBU922
DYNJ37254I1019348984967740193489849678UDI/DI 10193489849677 (EA) 40193489849678 (CS), Lot Numbers: 21EBB287, 21FBS039, 21KBB916, 21WBA934, 22BBP179, 22DBN656, 22FBE094, 22IBA792, 22IBC342, 23BBD691, 23BBP725, 23CBS713, 23IBR830, 23KBB006
DYNJ37254J1019532759527240195327595273UDI/DI 10195327595272 (EA) 40195327595273 (CS), Lot Numbers: 24CBN777, 24EBV639, 24GBP625, 24HBL327
DYNJ37383C1088994246525540889942465256UDI/DI 10889942465255 (EA) 40889942465256 (CS), Lot Numbers: 23HBK851
DYNJ37551A1088827758572040888277585721UDI/DI 10888277585720 (EA) 40888277585721 (CS), Lot Numbers: 23HBO656
DYNJ40094B1088827720871140888277208712UDI/DI 10888277208711 (EA) 40888277208712 (CS), Lot Numbers: 19AKD477, 19BKD188, 19DKA822, 19FKC285, 19HKB997, 19JMB401, 19LMC591, 20BMB740, 20BMC380, 20DMA323
Amount recalled
48655 units

This recall covers 18 products

The agency filed one notice per product. You are reading one of them; the other 17 are below.

5 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.

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, 6:54 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.