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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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Medium RiskFDA Device
Medical Devices/Surgical Equipment

Medline Medical Kits Recalled for Detachable Biopsy Valve Fragments

Agency Publication Date: April 1, 2026
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Summary

Medline Industries, LP is recalling 14,379 various medical kits because they contain Olympus single-use biopsy valves that may detach rubber fragments during use. The manufacturer, Olympus, is investigating an increase in complaints regarding these valves breaking apart at the slit. These fragments can become lodged in a patient's airway, requiring medical intervention to remove the foreign body. The kits were distributed nationwide across 13 states including California, Florida, Illinois, and Texas.

Risk

If the rubber biopsy valve fragments detach, they can enter the patient's tracheobronchial tree, causing an inflammatory response, low blood oxygen levels (hypoxia), or the need for additional procedures to remove the debris.

What You Should Do

  1. Identify if you have any of the affected Medline kits, such as the Airway Exam Kit, Bronch Pack, Pulmonary Pack, or Thoracic Robotics kits, by checking the product name and catalog number on the outer packaging.
  2. Check the lot number and Unique Device Identifier (UDI) printed on the product label or case carton to confirm if your specific unit is part of the recall. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled medical kits immediately.
  4. Contact Medline Industries, LP or your medical supply distributor to arrange for the return, replacement, or correction of the affected kits.
  5. Call the FDA Consumer Complaint hotline at 1-888-463-6332 for additional information regarding this medical device recall.

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: Airway Exam Kit
Model / REF:
DYKE1796
Lot Numbers:
24CBT023
24FBB701
24LBL343
25GBP141
UDI:
10193489874716
40193489874717

Recall #: Z-1705-2026

Product: BRONCH PACK
Model / REF:
DYKE2096
Lot Numbers:
26AMG895
UDI:
10198459629334
40198459629335

Recall #: Z-1706-2026

Product: NON MB BRONCHOPSCOPY CCH LH PK
Model / REF:
DYNJT6182
Lot Numbers:
25LBJ366
26ABR365
UDI:
10198459545283
40198459545284

Recall #: Z-1706-2026

Product: PULMONARY BRONCH PACK
Model / REF:
DYNDA2861A
Lot Numbers:
24EBA317
24EBV431
24IBD694
24JBQ783
UDI:
10195327471859
40195327471850

Recall #: Z-1706-2026

Product: THORACIC ROBOTS
Model / REF:
DYNJ908777B
Lot Numbers:
25EBD732
25GBG733
25IBQ613
25JBD457
25KBT352
26ABA235
26ABP735
UDI:
10198459269196
40198459269197

Recall #: Z-1707-2026

Product: BAL KIT
Model / REF:
DYNDA2137B
Lot Numbers:
24DBW065
24EBV301
24HBB492
24JBW143
25ABG413
25CBH359
25DBD213
25GBP569
25HBQ088
25KBF725
26ABE643
UDI:
10195327501259
40195327501250

Recall #: Z-1708-2026

Product: ENDO KIT
Model / REF:
DYKE1915
Lot Numbers:
24FBM018
24GBL319
UDI:
10195327371029
40195327371020

Recall #: Z-1708-2026

Product: BRONCHOSCOPY KIT (DYNJ900898I)
Model / REF:
DYNJ900898I
Lot Numbers:
25DME064
25HMD841
25JMD489
25KME329
25KMH848
25LMC029
25LMH235
25LMK305
UDI:
10198459273513
40198459273514

Recall #: Z-1709-2026

Product: BRONCHOSCOPY KIT (DYNJ901922G)
Model / REF:
DYNJ901922G
Lot Numbers:
24KBP812
UDI:
10195327640422
40195327640423

Recall #: Z-1709-2026

Product: FLEXIBLE BRONCHOSCOPY KIT (DYKM1417I)
Model / REF:
DYKM1417I
Lot Numbers:
24DLA405
24ELA912
24GLA871
24ILA151
24JLA326
UDI:
10195327456757
40195327456758

Recall #: Z-1709-2026

Product: FLEXIBLE BRONCHOSCOPY KIT (DYKM1417J)
Model / REF:
DYKM1417J
Lot Numbers:
25BLA761
25BLA886
25DLA353
25ELA056
25FLA429
25HLA196
25HLA242
25KLA388
25KLA610
UDI:
10198459191640
40198459191641

Recall #: Z-1709-2026

Product: LARYNGOSCOPY/BRONCHOSCOPY PACK (DYNJ58146A)
Model / REF:
DYNJ58146A
Lot Numbers:
23KDA851
24ADC096
24CDB107
24DDB887
24IDA855
24JDB494
24LDA691
25BMF825
25DMD969
25FMC760
25GMD422
UDI:
10193489611977
40193489611978

Recall #: Z-1709-2026

Product: RIGID KIT
Model / REF:
DYNDA2138A
Lot Numbers:
24DBM325
24DBM383
25DBK159
UDI:
10193489874594
40193489874595

Recall #: Z-1709-2026

Product: BRONCH PROCEDURE KIT
Model / REF:
DYKE2091
Lot Numbers:
25LBR616
UDI:
10198459606397
40198459606398

Recall #: Z-1710-2026

Product: BRONCHSCOPY (DYNJ900898G)
Model / REF:
DYNJ900898G
Lot Numbers:
23JBI824
23KBJ535
24ABR789
24ABV917
24BBU610
24DMK530
24FMF039
24GME122
24JMB670
24KMH657
25AMA403
25BME938
UDI:
10195327479473
40195327479474

Recall #: Z-1710-2026

Product: BRONCHSCOPY (DYNJ901922I)
Model / REF:
DYNJ901922I
Lot Numbers:
25BBL628
25FBM655
25HBW072
25KBO230
UDI:
10198459237270
40198459237271

Recall #: Z-1710-2026

Product: BRONCHSCOPY PACK
Model / REF:
DYNJ38313B
Lot Numbers:
24BBR676
24CBF032
24FBD924
24JBE567
25EBA277
25FBO580
25IBI418
UDI:
10884389857700
40884389857701

Recall #: Z-1710-2026

Product: BRONCHOSCOPY PACK 0120367-LF (DYNJ32750G)
Model / REF:
DYNJ32750G
Lot Numbers:
23KME954
23LMD492
24BMF722
24FMH267
24HMC509
UDI:
10889942212491
40889942212492

Recall #: Z-1710-2026

Product: BRONCHOSCOPY PACK 0120367-LF (DYNJ32750I)
Model / REF:
DYNJ32750I
Lot Numbers:
25BMA765
25DMC474
25EMI991
25IME718
26AMJ190
UDI:
10198459245695
40198459245696

Recall #: Z-1710-2026

Product: KIT, WR THORACIC
Model / REF:
DYNJ911252
Lot Numbers:
25EBU007
25LBC286
25LBI365
26ABC803
26ABU372
UDI:
10198459305030
40198459305031

Recall #: Z-1710-2026

Product: LARYNGOSCOPY/BRONCHOSCOPY PACK (DYNJ58146B)
Model / REF:
DYNJ58146B
Lot Numbers:
25HMG837
25JMJ636
26AMJ160
UDI:
10198459478253
40198459478254

Recall #: Z-1710-2026

Product: LEX THORACIC (DYNJ902016K)
Model / REF:
DYNJ902016K
Lot Numbers:
23JBL313
23KBX206
24ABG361
24ABS317
24CBU624
24DBT777
24EBP517
24IBB815
24LBH029
24LBK316
25BBD830
25BBK993
25DBQ241
25DBR926
UDI:
10195327391706
40195327391707

Recall #: Z-1710-2026

Product: LEX THORACIC (DYNJ902016L)
Model / REF:
DYNJ902016L
Lot Numbers:
25HBV912
25IBT298
25KBT137
UDI:
10198459452703
40198459452704

Recall #: Z-1710-2026

Product: ORGAN PROCUREMENT
Model / REF:
DYNJ908686
Lot Numbers:
23LBG479
UDI:
10195327145330
40195327145331

Recall #: Z-1710-2026

Product: PULMONARY PACK (DYKE1859)
Model / REF:
DYKE1859
Lot Numbers:
23LBU165
24ABT730
24CBL345
24FBK106
24HBJ512
25DBS024
25EBL346
UDI:
10195327171469
40195327171460

Recall #: Z-1710-2026

Product: THORACIC
Model / REF:
DYNJ901666L
Lot Numbers:
24DDC241
24EDB399
UDI:
10193489986815
40193489986816

Recall #: Z-1710-2026

Product: THORACIC ROBOTICS
Model / REF:
DYNJ908777A
Lot Numbers:
23JBV709
23KBC057
23LBP026
23LBP071
23LBP286
24BBH036
24DBD851
24FBC615
24GBH920
24HBS270
24KBL822
25ABE547
25BBP040
25BBR359
25CBA577
UDI:
10195327415174
40195327415175

Recall #: Z-1710-2026

Product: THORACOTOMY/THORACOSCOPY (DYNJ900482N)
Model / REF:
DYNJ900482N
Lot Numbers:
23KDB600
24ADA178
UDI:
10195327509941
40195327509942

Recall #: Z-1710-2026

Product: THORACOTOMY/THORACOSCOPY (DYNJ900482O)
Model / REF:
DYNJ900482O
Lot Numbers:
24CDA456
24EDC051
24GDB830
24IDB049
24JDB140
24KDA731
25ADB869
25BDA267
25CMD906
UDI:
10195327596569
40195327596560

Recall #: Z-1710-2026

Product: XPS
Model / REF:
DYNJ907605
Lot Numbers:
23JBA743
23JBI519
23LBQ647
24ABX014
24BBQ594
UDI:
10193489468052
40193489468053

Recall #: Z-1710-2026

Product: MEDLINE ANTERIOR HIP PACK
Model / REF:
DYNJ64672B
Lot Numbers:
23LMD300
UDI:
10195327377496
40195327377497

Recall #: Z-1711-2026

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98530
Status: Active
Manufacturer: Medline Industries, LP
Sold By: Authorized Medical Distributors; Hospitals; Surgical Centers
Manufactured In: United States
Units Affected: 7 products (14,379 kits total)
Distributed To: California, Florida, Illinois, Indiana, Kentucky, Massachusetts, Maryland, Montana, New York, Ohio, Pennsylvania, Tennessee, Texas

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.