Z-0354-2022 Class II Ongoing
FDA device recall Z-0354-2022 was initiated by Argon Medical Devices, Inc on October 4, 2021 and is designated Class II. Reason for recall: Due to component (housing and plunger) detaching from the semi-automatic biopsy instruments. The recall status is ongoing. Affected quantity: 79,910 devices.
Recall Details
- Product Type
- Devices
- Report Date
- December 15, 2021
- Initiation Date
- October 4, 2021
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 79,910 devices
Product Description
Reason for Recall
Distribution Pattern
Worldwide distribution - U.S. Nationwide distribution in the states of AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, and WV. The countries of ALB, ARE, ARG, AUS, AUT, BEL, BGD, BRA, CAN, CHE, CHL, CHN, COL, CZE, DEU, ECU, ESP, EST, FRA, GBR, GRC, HKG, HUN, IND, IRN, ISR, ITA, JOR, JPN, MAR, MEX, MYS, NLD, NPL, NZL, PAK, PER, PHL, POL, PRT, SAU, SGP, SRB, THA, TUR, and TWN.