FDA recall record

Allergan PLC McGhan Croissant-Shaped Tissue Expanders, Style 134 Product Usage: intended for recall — FDA Z-2458-2019

The action was initiated following notification by the U.S. FDA of their recently updated, global safety information concerning the higher incidence of…

Class Iclassification
Z-2458-2019official record ID
Sep 18, 2019report date

Recall record at a glance

Official recordZ-2458-2019
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmAllergan PLC
Report dateSep 18, 2019
Recall initiation dateJul 24, 2019
Quantity4,026,287 Breast Implants and Tissue Expanders Combined in total
LocationIrvine, CA, United States

Official product description

McGhan Croissant-Shaped Tissue Expanders, Style 134 Product Usage: intended for temporary subcutaneous implantation and require periodic, incremental inflation with sterile saline for injection until the desired amount of tissue is developed.

Why the product was recalled

The action was initiated following notification by the U.S. FDA of their recently updated, global safety information concerning the higher incidence of anaplastic large cell lymphoma (BIA-ALCL) in patients who have textured breast implants.

Distribution information

Worldwide Distribution and US Nationwide All fifty (50) US States, the US Virgin Islands and Puerto Rico. (AK, 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, WA, WI, WV, WY). OUS: Bermuda, Canada, Chile, Japan, Korea, Thailand, Taiwan and Vietnam.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

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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