Devices which did not undergo thermoforming could deform and lose performance.
Reason for recall: Devices which did not undergo thermoforming could deform and lose performance. Distribution: Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, DC, DE, FL, GA, GU, HI, IA, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY and International: TBD. Quantity: 1072 units (OUS only) Lot/code info: Model/Catalog Number: KD-401Q-0720; Material REF: 5856830; UDI-DI: 04953170041648; All Lots with a valid expiration date
04953170041648
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.