- Recalling firm
- International Life Sciences
- Reason for recall
- Augmentation devices failed bacterial endotoxin testing.
- Distribution pattern
- Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NY, OH, OK, OR, PA, SD, TN, TX, UT, VA, WA, WI, WY and the countries of Australia, France, Germany, Italy, Japan, Korea, Spain, Switzerland, United Kingdom, United Arab Emirates, Slovenia.
- State
- GA
- Status
- Ongoing
- Recall number
- Z-1556-2026
- Recall initiated
- February 6, 2026