Drugs & medicalClass II

Acumed LLC recalls 4.0mm x 10mm Cannulated Screw, Short Thread; Part number 3005-40010

Cannulated Screws 4.0mm x 10mm and 4.0mm x 12mm may not have sufficient axial pullout strength for the indicated use. Remote possibility of resulting in a mal or nonunion of the bone fragments, iatrogenic fracture,…

Read the official notice →
Date
2022-04-27
Country
United States
Brand
Acumed
Product
4.0mm x 10mm Cannulated Screw, Short Thread; Part number 3005-40010
Classification
Class II
Units
Worldwide distribution - US Nationwide distribution in the states of AK, AL,…
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Acumed recalls

  1. 2026-07-01
  2. US
    Drugs & medicalClass II

    Acumed LLC recalls Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Screw; 3070-27009 2.7mm x 9mm NL Hexalobe Screw;…

    Due to manufacturing error, hexalobe screws used with wrist fixation system may break during use.

    FDA · DeviceAcumed LLCUS Nationwide distribution in the states of AR, CA, CO, CT, FL, GA, IL, KS,…Official notice →
  3. 2024-03-06
  4. US
    Drugs & medicalClass II

    Acumed LLC recalls Acu-Loc and Acu-Loc 2 bone plates, screws and accessories for the following REF: 70-0045 Acu-Loc VDU Plate Standard, Left; 70-0045-S…

    Distribution without Pre-Market Clearance

    FDA · DeviceAcumed LLCWorldwide distribution - US Nationwide and the countries of AE, AR, AU, BE,…Official notice →
  5. 2024-01-03
  6. US
    Drugs & medicalClass II

    Acumed LLC recalls RibLoc U Plus 90 Instrument PRIMARY GUIDE ASSY, LOW PROFILE REF RBL2320 The RBL2320, Low Profile Primary Guide is an instrument used with…

    Due to potential breakage during use.

    FDA · DeviceAcumed LLCWorldwide - U.S. Nationwide distribution including in the states of AL, AZ,…Official notice →
  7. 2023-01-04
  8. US
    Drugs & medicalClass II

    Acumed LLC recalls 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…

    Distribution without Pre-Market Clearance

    FDA · DeviceAcumed LLCWorldwide - U.S. Nationwide distribution including in the states of AK, AL,…Official notice →
All 5 Acumed recalls →

Other drugs & medical recalls in the United States

  1. 2022-04-27
  2. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls SIEMENS SOMATOM with software syngo CT VA30A_SP4 Models: SOMATOM go.Now 11061610 & 11061618 SOMATOM go.Up 11061620 & 11061628…

    Software error may result in sporadic problems causing scanning workflow interruptions, unexpected user notifications and image artifacts. Sporadic software errors may also occur during interventional workflows.…

    FDA · DeviceSiemens Medical Solutions USA, IncNationwideOfficial notice →
  3. US
    Drugs & medicalClass II

    Medtronic Xomed, Inc. recalls Software 1898072 IPC upgrade v 2.7.3.0, IPC System: a) CONSOLE 1898001 IPC, Product Number 1898001; b) CONSOLE IPC REFURB, Product Number…

    As a result of Medtronic's integrated power console (authentication number: 222ACBZX00018000) being used with software version: v2.7.3.0, it was discovered that there was a defect that resulted in a difference between…

    FDA · DeviceMedtronic Xomed, Inc.International distribution country of Japan.Official notice →
  4. US
    Drugs & medicalClass II

    Huntleigh Healthcare Ltd. recalls HUNTLEIGH Disposable intraoperative Probe, 8Mhz (box), REF DIPP10, containing 10 individual Disposable Intraoperative Probes, REF DIOP8

    Faceplate may become detached from the probe body.

    FDA · DeviceHuntleigh Healthcare Ltd.US Nationwide distribution in the states of OK, CA, GA, MI, VA.Official notice →
  5. US
    Drugs & medicalClass II

    Abbott recalls Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter, Bi-D, Curve DD, Model A-TCSE-DD, Sterile.

    Devices were manufactured with a "First Use Date" preprogrammed in the EEPROM which disables the use of the single-use device.

    FDA · DeviceAbbottWorldwide distribution - US Nationwide - there was government distribution but…Official notice →
  6. US
    Drugs & medicalClass II

    Microbiologics Inc recalls Inactivated macrolide-resistant Mycoplasma genitalium

    The QC process was not adequate for the specification range.

    FDA · DeviceMicrobiologics IncUS Nationwide distribution in the states of NV and VT.Official notice →
  7. US
    Drugs & medicalClass II

    Microbiologics Inc recalls Inactivated macrolide and quinolone-resistant Mycoplasma genitalium

    QC process was not adequate for the specification range.

    FDA · DeviceMicrobiologics IncUS Nationwide distribution in the state of TX.Official notice →
See all drugs & medical recalls →