FDA recall record

Mentor MemoryGel Breast Implant recall — FDA Z-2326-2016

The box of 300cc MemoryGel Breast Implant was labeled with null manufacturing and expiration dates.

Class IIclassification
Z-2326-2016official record ID
Aug 10, 2016report date

Recall record at a glance

Official recordZ-2326-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMentor Texas, LP.
Report dateAug 10, 2016
Recall initiation dateJul 1, 2016
Quantity35 units
LocationIrving, TX, United States

Official product description

Mentor MemoryGel Breast Implant; Indicated for females for breast augmentation and breast reconstruction.

Why the product was recalled

The box of 300cc MemoryGel Breast Implant was labeled with null manufacturing and expiration dates.

Distribution information

Distributed in the states of NY, WI, CA, TX, CO, NC, NJ, OH, TN, RI, and IL.

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

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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