ClearanceBrief
Recall Z-0768-2023 ยท HWC Screw, Fixation, Bone

Acumed LLC

Acutrak 2 Part Number/Part Description: 30-0021 25.0mm Acutrak 2 - 5.5 Screw 30-0021-S 25.0mm Acutrak 2 - 5.5 Screw 30-0023 30.0mm Acutrak 2 - 5.5 Screw 30-0023-S 30.0mm Acutrak 2 - 5.5 Screw 30-0025 35.0mm Acutrak 2 - 5.5 Screw 30-0025-S 35.0mm Acutrak 2 - 5.5 Screw 30-0027 40.0mm Acutrak 2 - 5.5 Screw 30-0027-S 40.0mm Acutrak 2 - 5.5 Screw 30-0029 45.0mm Acutrak 2 - 5.5 Screw 30-0029-S 45.0mm Ac

DateDec 23, 2022 (initiated Nov 29, 2022)
StatusOpen, Classified
ReasonDistribution without Pre-Market Clearance
Root causeNo Marketing Application
ActionOn 11/29-30/2022, Acumed LLC sent an "URGENT: MEDICAL DEVICE CORRECTION" Letter via USPS First Class with signature required to customers informing them that the Acutrak Headless Compression Screws and the Acutrak 2 Headless Compression Screw Systems were commercialized with a Pre-Market Clearance (510(k)). Customer are instructed to: Product within the scope of this correction does not need to be returned to Acumed. No actions are required as this is a compliance issue and not a patient safety issue. This notification is solely for your awareness. However, physicians are urged to notify Ac
Quantity1,681,860 units (Acutrak 2 286,026; Micro Acutrak 2 524,566; Mini Acutrak 2 609,220; Standard Acutrak 262,048)
DistributionWorldwide - U.S. Nationwide distribution including in the states of 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, VI, VT, WA, WI, WV, and WY. The countries of AE,
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K221333Acumed Acutrak System- MR Conditional, Acumed Acturak 2 System- MR Conditional
Acumed, LLC, Dec 29, 2022