FDA recall, , Moderate risk
Medline Kits With B. Braun IV Administration Sets
Medline kits containing B. Braun IV administration sets may have check valves that stick.
What happened
Medline Industries, LP of Northfield, Illinois, is recalling Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets. The kits contain B. Braun IV Administration Sets and Pump Administration Sets that were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions. The recall began November 26, 2025, and was added to the FDA's Enforcement Report on January 12, 2026. Distribution was US Nationwide.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its UDI-DI and lot code are listed under that product.
A UDI-DI is the device identifier printed with the barcode on the device label.
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets
- UDI-DI
- 10193489587869
- 40193489587860
- Lot code
- 25HBQ850
- UDI-DI
- 10884389725092
- 40884389725093
- Lot code
- 25IBC144
- UDI-DI
- 10195327521660
- 40195327521661
- 10195327691349
- 40195327691340
- 10195327503185
- 40195327503186
- 10198459415678
- 40198459415679
- 10198459467493
- 40198459467494
- 10198459399893
- 40198459399894
- 10198459435126
- 40198459435127
- 10198459269523
- 40198459269524
- 10195327343163
- 40195327343164
- 10198459447877
- 40198459447878
- 10198459370595
- 40198459370596
- 10198459411700
- 40198459411701
- 10198459489372
- 40198459489373
- 10198459377129
- 40198459377120
- 10198459347702
- 40198459347703
- 10198459024320
- 40198459024321
- 10198459399732
- 40198459399733
- 10198459032448
- 40198459032449
- 10198459291272
- 40198459291273
- 10198459078415
- 40198459078416
- 10195327411213
- 40195327411214
- 10198459025648
- 40198459025649
- 10195327387433
- 40195327387434
- 10195327549374
- 40195327549375
- 10198459557330
- 40198459557331
- 10198459011368
- 40198459011369
- 10195327482602
- 40195327482603
- 10195327549343
- 40195327549344
- 10198459477942
- 40198459477943
- 10198459508561
- 40198459508562
- 10198459544545
- 40198459544546
- 10198459550539
- 40198459550530
- 10198459547201
- 40198459547202
- 10198459528651
- 40198459528652
- Lot code
- 25HBB410
- 25HBE055
- 25HBF057
- 25HBI512
- 25HBK906
- 25HBV987
- 25HLA076
- 25HLA432
- 25HLA829
- 25HMB303
- 25HMB948
- 25HMC488
- 25HMD440
- 25HMF480
- 25IBC508
- 25IBI706
- 25IBK720
- 25IBL590
- 25IBL885
- 25IBQ969
- 25IBU385
- 25IBW167
- 25ILA943
- 25ILA944
- 25IME692
- 25JBB244
- 25JBC342
- 25JBE269
- 25JBE865
- 25JBG502
- 25JBJ439
- 25JBJ451
- 25JBL575
- 25JBO961
- 25JBR391
- 25JBS091
- 25JBU194
- 25JBU341
- 25JBU577
- 25JLA660
- 25JLA986
- 25JLB077
- 25JMD403
- 25JMD404
- 25JMF248
- 25JMH456
- 25JML466
- 25KBC077
- 25KBH159
- 25KBL301
- 25KLA016
- 25KLA028
- 25KLA029
- 25KLA107
- 25KME034
- 25KME090
- UDI-DI
- 10195327608309
- 40195327608300
- 10198459285615
- 40198459285616
- 10195327373504
- 40195327373505
- 10195327658472
- 40195327658473
- 10195327065911
- 40195327065912
- Lot code
- 25JBB147
- 25KBL305
- 25HBT834
- 25IBJ757
- 25JBJ557
- 25JLA480
- 25HBI335
- 25IBE523
- 25JBM702
- 25IBV942
- UDI-DI
- 10889942695911
- 40889942695912
- 10198459418143
- 40198459418144
- 10198459316593
- 40198459316594
- 10195327461294
- 40195327461295
- 10195327482893
- 40195327482894
- 10193489432794
- 40193489432795
- 10193489571875
- 40193489571876
- 10193489468243
- 40193489468244
- 10198459258848
- 40198459258849
- Lot code
- 25GBY100
- 25HBI736
- 25HBL296
- 25HBN030
- 25HLA445
- 25HMA140
- 25IBI197
- 25IBL774
- 25IMG620
- 25IMH657
- 25IMH924
- 25JBH529
- 25JBO555
- 25JLA937
- 25KBB119
- 25KBH512
- UDI-DI
- 10193489484953
- 40193489484954
- 10195327223670
- 40195327223671
- 10198459027765
- 40198459027766
- 10195327432713
- 40195327432714
- 10195327576998
- 40195327576999
- 10889942519583
- 40889942519584
- 10193489711981
- 40193489711982
- 10193489849707
- 40193489849708
- 10193489403831
- 40193489403832
- 10193489235425
- 40193489235426
- 10193489305708
- 40193489305709
- 10193489305715
- 40193489305716
- 10195327058890
- 40195327058891
- 10193489969962
- 40193489969963
- 10195327216498
- 40195327216499
- 10889942731299
- 40889942731290
- 10198459004841
- 40198459004842
- Lot code
- 25IDB125
- 25IDB400
- 25JDB835
- 25KDA036
- 25KDA248
- 25IDA545
- 25JDB867
- 25KDA768
- 25HDB656
- 25IDA638
- 25JDA666
- 25HDA878
- 25IDA087
- 25IDA817
- 25JDB317
- 25IBL412
- 25KBK165
- 25IMD671
- 25JMG868
- 25KME757
- 25HBF059
- 25JBU391
- 25IBT744
- 25KBG976
- 25JBS281
- 25HBJ008
- 25HBV936
- 25IBB540
- 25HBF086
- 25IBF923
- 25IBR790
- 25HBF087
- 25IBS865
- 25HBG750
- 25GMK728
- 25HMI417
- UDI-DI
- 10198459313745
- 40198459313746
- 10198459364556
- 40198459364557
- 10195327674229
- 40195327674220
- 10198459392603
- 40198459392604
- Lot code
- 25HMC337
- 25KBG419
- 25IBU284
- 25KBJ623
- 25HBU964
- 25IBV819
- 25KBF028
- UDI-DI
- 10889942695911
- 40889942695912
- 10198459418143
- 40198459418144
- 10198459316593
- 40198459316594
- Lot code
- 25IBT843
- 25IMA327
- 25IMI028
- UDI-DI
- 10195327656454
- 40195327656455
- 10198459503023
- 40198459503024
- Lot code
- 25HMB184
- 25JMH400
- UDI-DI
- 10195327634698
- 40195327634699
- Lot code
- 25HLA435
- 25HLB046
- UDI-DI
- 10195327386726
- 40195327386727
- 10198459523434
- 40198459523435
- 10195327566449
- 40195327566440
- 10198459310911
- 40198459310912
- Lot code
- 25HMC849
- 25IMG807
- 25JMF937
- 25JMD518
- 25HMD322
- 25JMG543
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: AN01 Carotid Anesth Kit-LF, Medline Kit SKU PHS972096014B
- UDI-DI
- 10889942695911
- 40889942695912
- Lot code
- 25JMC398
Recall details
- Company began the recall
- Sold in
US Nationwide distribution.
- Company
- Medline Industries, LPNorthfield, Illinois
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98154
- Recall numbers
- Z-1049-2026 to Z-1060-2026
All recalls from Medline Industries, LP
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary



