FDA recall record

Boston Scientific EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Outer recall — FDA Z-0396-2024

Poor image quality due to fluid ingress in the lens.

Class IIclassification
Z-0396-2024official record ID
Nov 29, 2023report date

Recall record at a glance

Official recordZ-0396-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmBoston Scientific Corporation
Report dateNov 29, 2023
Recall initiation dateSep 27, 2023
QuantityUS: 586 devices & OUS: 81 devices
LocationMarlborough, MA, United States

Official product description

EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Outer box UPN# M0054242CE0.

Why the product was recalled

Poor image quality due to fluid ingress in the lens.

Distribution information

Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA VT, WA, WI & WV. The countries of Australia, Belgium, Canada, Czech Republic, Denmark, France, Germany, Great Britain, Italy, New Zealand, Spain, Sweden, Switzerland.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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