FDA recall record

Coloplast Manufacturing US Ureteral dilator, REF RBD014 recall — FDA Z-1463-2024

A possible sterility issue (e.g. a breach in sterile packaging) was detected in Coloplast's facility on some ureteral dilator products. This issue on the…

Class IIclassification
Z-1463-2024official record ID
Apr 10, 2024report date

Recall record at a glance

Official recordZ-1463-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmColoplast Manufacturing US, LLC
Report dateApr 10, 2024
Recall initiation dateMar 11, 2024
Quantity710 units
LocationMinneapolis, MN, United States

Official product description

Ureteral dilator, REF RBD014

Why the product was recalled

A possible sterility issue (e.g. a breach in sterile packaging) was detected in Coloplast's facility on some ureteral dilator products. This issue on the ureteral dilator packaging has been identified during testing in our facility.

Distribution information

US: GA, MS, TN, MN, AZ,N MD, LA, KS, WA

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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