FDA recall record

Axonics Modulation Technologies BULKAMID, URETHRAL BULKING SYSTEM model # 50050 containing recall — FDA Z-2077-2021

Lack of Sterility Assurance; needle in procedure pack labeled as sterile may not have been adequately sterilized

Class IIclassification
Z-2077-2021official record ID
Jul 21, 2021report date

Recall record at a glance

Official recordZ-2077-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAxonics Modulation Technologies, Inc.
Report dateJul 21, 2021
Recall initiation dateJun 3, 2021
Quantity2,702 units
LocationIrvine, CA, United States

Official product description

BULKAMID, URETHRAL BULKING SYSTEM model # 50050 containing the component: Bulkamid Needle, REF 230651221C, 2 G x 12 am, sterile, CE 0476

Why the product was recalled

Lack of Sterility Assurance; needle in procedure pack labeled as sterile may not have been adequately sterilized

Distribution information

US nationwide distribution.

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: not stated.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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