FDA recall record

Merit Medical Systems Scout MD, REF MDS05A-01, MDS05C-01, MDS10C-01 Contents: (1) Scout MD recall — FDA Z-0187-2027

The implantable clip may experience difficulties deploying, which could prevent the reflector from functioning as intended during use.

Class IIclassification
Z-0187-2027official record ID
Oct 21, 2026report date

Recall record at a glance

Official recordZ-0187-2027
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmMerit Medical Systems, Inc.
Report dateOct 21, 2026
Recall initiation dateAug 27, 2026
LocationSouth Jordan, UT, United States

Official product description

Scout MD, REF MDS05A-01, MDS05C-01, MDS10C-01 Contents: (1) Scout MD Delivery System, Standard for use with the SCOUT MD Surgical Guidance System, Rx Only, Sterile-EO

Why the product was recalled

The implantable clip may experience difficulties deploying, which could prevent the reflector from functioning as intended during use.

Distribution information

US: AZ, CA, FL, IN, LA, NV, RI OUS: None

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: E-Mail.

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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