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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Device
Medical Devices

Medline Anesthesia Circuit Kits Recalled for Tubing Cracks and Leaks

Agency Publication Date: November 13, 2025
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Summary

Medline Industries, LP has recalled 96,406 anesthesia circuit kits and various surgical convenience kits because the 120-inch expandable tubing may develop cracks. These cracks can lead to gas leaks during surgery, potentially preventing patients from receiving enough oxygen or the correct amount of anesthesia. Medline has received multiple complaints regarding these leaks, which could result in serious injury or death.

Risk

Cracks in the anesthesia tubing can cause leaks that result in hypoxia (lack of oxygen), hypoventilation (poor breathing), or the inadequate delivery of anesthesia gases to a patient. Additionally, volatile anesthetic gases may leak into the operating room, posing a risk to healthcare staff.

What You Should Do

  1. This recall affects Medline Anesthesia Circuit Kits and various surgical convenience kits containing 120-inch expandable tubing, used in anesthesia and various surgical procedures.
  2. Check the product label or packaging for catalog numbers (e.g., DYNJAA10591, DYNJ10550, DYNJ909116D) and lot numbers (e.g., 25EBU353, 25GBI473). See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled products immediately.
  4. Contact Medline Industries, LP or your distributor directly to arrange for the return, replacement, or correction of the affected kits.
  5. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) if you have additional questions or concerns.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Anesthesia Circuit Kits and various surgical kits
Variants: ADULT 120 EXPANDABLE W/MASK, ANES CIRC 120IN EXP-LF, ANES CIRCUIT ADULT 120"-LF, ANESTHESIA 120" ADLT-LF, ANESTHESIA CIRC ADULT 120-LF, ANESTHESIA CIRCUIT - LF, ANESTHESIA CIRCUIT 120EXP-LF, ANESTHESIA CIRCUIT ADULT-LF, ANESTHESIA CIRCUIT-LF, CIRC 120" EXP 1 BV HMEF 3L GSL, EXPANDABLE CIRCUIT-LF, NM ANESTHESIA TURNOVER KIT, PROV HEALTH HEPA CIRC #2-LF, SPTMPX01IA CIRCUIT ADULT-LF
Model / REF:
DYNJAA10591
DYNJAA6555G
DYNJAA10817
DYNJAA10775
DYNJAA10601
DYNJAA10261B
DYNJAA10741A
DYNJAA0380A
DYNJAA10641
DYNJAA10706B
DYNJAA10851
DYNJAA10922B
DYNJAA10971A
DYNJAA11030A
DYNJAA11087
DYNJAA11126
DYNJAA0309A
DYNJAA0368A
DYNJAA10368A
DYNJAA10392
DYNJAA10430A
DYNJAA10547A
DYNJAA10639A
DYNJAA10656A
DYNJAA10685A
DYNJAA10685B
DYNJAA10920
DYNJAA11095
DYNJAA0433
DYNJAA0360
DYNJAA10973A
Lot Numbers (58):
25EBU353
25GBI473
25EBU304
25GBQ732
25GBH582
25FBB950
25FBT875
25GBX623
25EBH621
25EBQ391
25FBJ760
25GBY374
25IBK072
25FBN032
25FBW335
25IBH048
25FBT853
25FBD876
25FBD877
25GBJ254
25GBJ256
25FBN184
25HBM893
25FBN043
25EBK360
25FBN055
25EBJ456
25FBL121
25FBT898
25FBT899
25FBH921
25GBK879
25GBN124
25GBN125
25EBK364
25FBQ326
25HBA472
25GBY311
25IBD803
25GBO619
25GBE789
25IBL075
25FBT844
25GBP694
25FBQ442
25GBO675
25GBA751
25FBQ349
25FBQ346
25FBG942
UDI (62):
40193489400268
10193489400267
40193489419000
10193489419009
40195327092550
10195327092559
40195327478286
10195327478285
40198459320706
10198459320705
40193489430784
10193489430783
40198459320720
10198459320729
40888277962201
10888277962200
40193489832052
10193489832051
40193489603188
10193489603187
40889942632535
10888942632534
40889942655435
10889942655434
40888277761958
10888277761957
40889942841227
10889942841226
40193489455527
10193489455526
40195327279142
10195327279141
40198459372293
10198459372292
40193489485982
10193489485981
40193489250573
10193489250572
40193489348102
10193489348101
40193489365338
10193489365337
40193489429467
10193489429466
40193489463386
10193489463385
40198459301880
10198459301889
40195327298167
10195327298166

Recall #: Z-0442-2026

Product: Anesthesia Circuit Kits - BREATHING KIT-LF
Model / REF:
DYNJ10550
Lot Numbers:
25EBQ445
UDI:
40889942469704
10889942469703

Recall #: Z-0443-2026

Product: Surgical Kits (OPEN HEART SUPPLEMENT, VASCULAR)
Variants: OPEN HEART SUPPLEMENT, VASCULAR
Model / REF:
DYNJ909116D
DYNJ909124F
Lot Numbers:
25FBM604
25GBP604
25FBB831
25GBI833
UDI:
40198459055356
10198459055355
40198459130619
10198459130618

Recall #: Z-0444-2026

Product: Surgical Kits (ENT, LARYNGOSCOPY - BRONCHOSCOPY)
Variants: ENT, LARYNGOSCOPY - BRONCHOSCOPY
Model / REF:
DYNJ909128I
DYNJ909114D
Lot Numbers:
25GBO685
25GBN602
UDI:
40198459333355
10198459333354
40198459055301
10198459055300

Recall #: Z-0445-2026

Product: Surgical Kits (ROBOTIC GASTRIC LAP SLEEVE, CYSTO, GENERAL LAPAROSCOPY)
Variants: ROBOTIC GASTRIC LAP SLEEVE-LF, CYSTO, GENERAL LAPAROSCOPY-LF
Model / REF:
DYNJ909119G
DYNJ909127F
DYNJ909129D
Lot Numbers:
25FBP819
25GBM605
25FBV537
25FBP681
UDI:
40198459055424
10198459055423
40198459055264
10198459055263
40198459130527
10198459130526

Recall #: Z-0446-2026

Product: Convenience Kit, BREAST HERNIA
Model / REF:
DYNJ909125G
Lot Numbers:
25FBU543
25IBD459
UDI:
40198459130664
10198459130663

Recall #: Z-0447-2026

Product: Convenience Kits (ORTHO SPINE, UROLOGY MINOR, SET UP, HIP PINNING)
Variants: ORTHO SPINE ST CLAIR, UROLOGY MINOR, SET UP, HIP PINNING
Model / REF:
DYNJ901048N
DYNJ909123F
DYNJ909132F
DYNJ909308D
Lot Numbers:
25FBB311
25GBC282
25GBW486
25GBQ070
25GBI845
25IBF708
25GBT826
25IBF707
UDI:
40198459055288
10198459055287
40198459055554
10198459055553
40198459130572
10198459130571
40198459130602
10198459130601

Recall #: Z-0448-2026

Product: Anesthesia circuit kit; CIRCUIT,ANES,EXTENDFLEX,120,LF
Model / REF:
DYNJAA10230
Lot Numbers:
25EBV570
25FBT843
UDI:
40884389688589
10884389688588

Recall #: Z-0449-2026

Product: Convenience kits (GYN ROBOTIC, ROBOTIC PROSTATE)
Variants: GYN ROBOTIC, ROBOTIC PROSTATE
Model / REF:
DYNJ901046M
DYNJ909120D
Lot Numbers:
25FBM810
25GBK307
25GBT821
25IBF809
UDI:
40198459130381
10198459130380
40198459130541
10198459130540

Recall #: Z-0450-2026

Product: Convenience kits (ORTHO SPINE, TOTAL JOINT, DR SALMA'S SPINE, PATTERSON TOTAL JOINT, KYPHOPLASTY)
Variants: ORTHO SPINE FUMICH, TOTAL JOINT, DR SALMA'S SPINE, PATTERSON TOTAL JOINT, KYPHOPLASTY
Model / REF:
DYNJ901047R
DYNJ902308K
DYNJ909111F
DYNJ909117G
DYNJ909113F
Lot Numbers:
25FBE036
25GBV759
25FBR230
25GBU693
25FBO307
25GBN625
25FBB321
25GBU688
25IBM788
UDI:
40198459130794
10198459130793
40198459130466
10198459130465
40198459130480
10198459130489
40198459130596
10198459130595
40198459130459
10198459130458

Recall #: Z-0451-2026

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97882
Status: Active
Manufacturer: Medline Industries, LP
Sold By: Authorized medical supply distributors; Medline Industries, LP
Manufactured In: United States
Units Affected: 10 products (96,406 total units)
Distributed To: Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, New Jersey, New York, Ohio, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, Tennessee, Texas, Washington, Wisconsin

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.