Recall record at a glance
| Official record | Z-0767-2023 |
|---|---|
| Category | Medical Device Recalls |
| Classification | Class II |
| FDA record status | Ongoing |
| Recalling firm | Acumed LLC |
| Report date | Jan 4, 2023 |
| Recall initiation date | Nov 29, 2022 |
| Quantity | Total 306,934 units (Acutrak 239,611 units and Mini Acutrak 67,323) |
| Location | Hillsboro, OR, United States |
Official product description
Part Number/Part Description: 30-0033-S 30mm Acutrak Fusion Device 6mm Nose AM-0025-S 25.0mm Acutrak 4/5 Bone Screw AM-0030-S 30.0mm Acutrak 4/5 Bone Screw AM-0035-S 35.0mm Acutrak 4/5 Bone Screw AM-0040-S 40.0mm Acutrak 4/5 Bone Screw AM-0045-S 45.0mm Acutrak 4/5 Bone Screw AM-0050-S 50.0mm Acutrak 4/5 Bone Screw AP-67100-S 100mm Acutrak 6/7 Fixation Screw AP-67105-S 105mm Acutrak 6/7 Fixation Screw AP-67110-S 110mm Acutrak 6/7 Fixation Screw AP-67115-S 115mm Acutrak 6/7 Fixation Screw AP-67120-S 120mm Acutrak 6/7 Fixation Screw AP-6740-S 40mm Acutrak 6/7 Fixation Screw AP-6745-S 45mm Acutrak 6/7 Fixation Screw AP-6750-S 50mm Acutrak 6/7 Fixation Screw AP-6755-S 55mm Acutrak 6/7 Fixation Screw AP-6760-S 60mm Acutrak 6/7 Fixation Screw AP-6765-S 65mm Acutrak 6/7 Fixation Screw AP-6770-S 70mm Acutrak 6/7 Fixation Screw AP-6775-S 75mm Acutrak 6/7 Fixation Screw AP-6780-S 80mm Acutrak 6/7 Fixation Screw AP-6785-S 85mm Acutrak 6/7 Fixation Screw AP-6790-S 90mm Acutrak 6/7 Fixation Screw AP-6795-S 95mm Acutrak 6/7 Fixation Screw ATF-140-S 14.0mm Acutrak Fusion Device ATF-160-S 16.0mm Acutrak Fusion Device ATF-180-S 18.0mm Acutrak Fusion Device ATF-200-S 20.0mm Acutrak Fusion Device ATF-220-S 22.0mm Acutrak Fusion Device ATF-240-S 24.0mm Acutrak Fusion Device ATF-270-S 27.0mm Acutrak Fusion Device ATF-320-S 32.0mm Acutrak Fusion Device ATF-370-S 37.0mm Acutrak Fusion Device ATM-100-S 10.0mm Mini Acutrak Fixation Screw ATM-120-S 12.0mm Mini Acutrak Fixation Screw ATM-140-S 14.0mm Mini Acutrak Fixation Screw ATM-160-S 16.0mm Mini Acutrak Fixation Screw ATM-180-S 18.0mm Mini Acutrak Fixation Screw ATM-200-S 20.0mm Mini Acutrak Fixation Screw ATM-220-S 22.0mm Mini Acutrak Fixation Screw ATM-240-S 24.0mm Mini Acutrak Fixation Screw ATM-260-S 26.0mm Mini Acutrak Fixation Screw
Why the product was recalled
Distribution without Pre-Market Clearance
Distribution information
Worldwide - 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, AR, AU, BE, BR, CA, CH, CL, CN, CO, CR, DE, DK, EC, ES, FI, FR, GB, GT, HK, IE, IL, IT, JP, KR, KW, MX, MY, PA, PE, PR, PT, QA, SA, SE, SG, TH, TR, TW, and ZA.
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Letter.
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
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.