Reported Nov 29, 2023 · Ongoing

EXALT Model D Single-Use Duodenoscope, 2 pack: Outer box UPN# M00542421, Inner box UPN # M00542420 & Outer box UPN#…

Boston Scientific Corporation

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: Boston Scientific Corporation · 100 Boston Scientific Way · Marlborough, MA · 01752-1234

Is this the product you have?

  • EXALT Model D Single-Use Duodenoscope, 2
  • packOuter box UPN# M00542421, Inner box UPN # M00542420 & Outer box UPN# M0054242CE1, Inner box UPN # M0054242CE0
Lot codes and dates
  • UDI-DI (GTIN)

    82 of 82 codes

    • 08714729993605
    • Outer box UPN# M00542421
    • Inner box UPN # M00542420
    • Lot / Batch # 31118200
    • 31537337
    • 31118202
    • 31538040
    • 31129470
    • 31544823
    • 31145980
    • 31544825
    • 31150536
    • 31590918
    • 31150537
    • 31591865
    • 31150538
    • 31607291
    • 31175587
    • 31619981
    • 31193809
    • 31627631
    • 31193810
    • 31636279
    • 31232040
    • 31643793
    • 31239963
    • 31676406
    • 31248263
    • 31683921
    • 31251918
    • 31692257
    • 31269307
    • 31697145
    • 31275008
    • 31706116
    • 31283026
    • 31710191
    • 31305347
    • 31718478
    • 31322088
    • 31726052
    • 31334176
    • 31729292
    • 31338402
    • 31734350
    • 31347461
    • 31738755
    • 31348990
    • 31738756
    • 31357937
    • 31754162
    • 31360721
    • 31762358
    • 31366683
    • 31764634
    • 31373783
    • 31767053
    • 31409362
    • 31774421
    • 31416272
  • UDI-DI (GTIN)
    • 08714729995753
    • Outer box UPN# M0054242CE1
    • Inner box UPN # M0054242CE0
    • Lot /Batch # 31118201
    • 31331654 31129503
    • 31817723
    • 31265893
Amount recalled
US: 5,709 devices & OUS: 180 devices

This recall covers 2 products

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

Where it was sold

Why it was recalled

Poor image quality due to fluid ingress in the lens.

This product could cause temporary or reversible health problems — stop using it.

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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, 5:36 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.