Drugs & medicalClass II

Smith & Nephew, Inc. recalls Smith and Nephew EVOS Self-Tapping Locking Screw SST: (1)REF 72413575, 3.5MM x 75MM, and (2) REF 72413570, 3.5MM X 70MM. Sterile.

The labels on the packages of screws were switched.

Read the official notice →
Date
2021-11-24
Country
United States
Brand
Smith & Nephew
Product
Smith and Nephew EVOS Self-Tapping Locking Screw SST: (1)REF 72413575, 3.5MM x 75MM, and (2) REF 72413570, 3.5MM X 70MM. Sterile.
Classification
Class II
Units
Distribution was made to AL, AZ, CA, CO, CT, FL, GA, IL, IN, KY, LA, MA, ME,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Smith & Nephew recalls

  1. 2022-07-27
  2. US
    Drugs & medicalClass II

    Smith & Nephew, Inc. recalls (1) Genesis II Non-Porous Tibial Baseplate Size 5 Right, Product #71420186. (2) Genesis II Non-Porous Tibial Baseplate Size 4 Left,…

    The product was mispackaged (swapped). The devices within the inner tray matches the inner tray but does not match the outer box label and the chart sticks.

    FDA · DeviceSmith & Nephew, Inc.US Nationwide distribution in the states of AZ, CA, GA, KS, LA, MN, MI, MO,…Official notice →
  3. 2022-05-25
  4. US
    Drugs & medicalClass II

    Smith & Nephew Inc recalls LEGION NARROW PS OXIN SZ 6N RT and JRNY II BCS FEMORAL OXIN LT SZ 5

    It was reported that a JOURNEY II BCS Femoral OXIN LT SZ5 was in a box labelled as a LEGION NARROW PS OXIN SZ 6N RT.

    FDA · DeviceSmith & Nephew IncWorldwide distribution - US Nationwide distribution in the states of CT, NC,…Official notice →
  5. 2022-02-16
  6. US
    Drugs & medicalClass II

    Smith & Nephew, Inc. recalls Acufex Access Advanced Positioning Kit - indicated for use to position and distract the extremity of patient during open and arthroscopic…

    Products were shipped to the Global Distribution Center instead of the sterilizer and therefore product did not undergo the sterilization process

    FDA · DeviceSmith & Nephew, Inc.Worldwide distribution - US Nationwide distribution in the states of CO, CT,…Official notice →
  7. 2022-02-09
  8. US
    Drugs & medicalClass II

    Smith & Nephew, Inc. recalls INTEGRA SURFIX ALPHA Screwdriver Torx 10, REF 219 135 ND

    The affected screwdrivers are out of specification and may not mate with the Surfix Alpha Lock screw

    FDA · DeviceSmith & Nephew, Inc.US Nationwide distribution in the states of CA and OH.Official notice →
  9. 2021-12-22
  10. US
    Drugs & medicalClass II

    Smith & Nephew, Inc. recalls smith&Nephew EVOS MEDIAL DISTAL FEMUR PLATE, L, 5H, 90MM, REF 72573101

    Testing vendor notified Smith & Nephew that previous MRI scanning conditions provided in Exponents reports were erroneous. Erroneous data from the reports was incorporated in the released IFU 81110294 EVOS Large…

    FDA · DeviceSmith & Nephew, Inc.US Nationwide distribution in the states of CO, FL, GA, MA, MN, MO, NC, NJ,…Official notice →
  11. 2021-10-27
  12. US
    Drugs & medicalClass II

    Smith & Nephew, Inc. recalls 6.5MMX165MM CANNULATED SCREW

    The product label incorrectly indicated that the screws are fully threaded, but the screws contained in the package were partially threaded.

    FDA · DeviceSmith & Nephew, Inc.Worldwide distribution - US Nationwide distribution in the states of OK, TN…Official notice →
All 22 Smith & Nephew recalls →

Other drugs & medical recalls in the United States

  1. 2021-12-01
  2. US
    Drugs & medicalClass III

    Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals recalls Butalbital, APAP, Caf 50/325/40 Tablet, packaged in a) 12-count bottles, NDC: 71335-1767-09, barcode…

    Labeling: Not Elsewhere Classified: the controlled substance classification "CIII" is missing on the label

    FDA · DrugBryant Ranch Prepack, Inc. dba BRP PharmaceuticalsNationwide in the USAOfficial notice →
  3. US
  4. 2021-11-24
  5. US
    Drugs & medicalClass II

    Roche Diagnostics Operations, Inc. recalls Cobas u 601 urinalysis test system, Catalog number 06334601001 The cobas U 601 urinalysis test system is comprised of the…

    A potential risk for false negative nitrite results exists when endogenous creatinine levels are 15,000 mg/L and above. No interference of Nitrite results was observed at creatinine levels up to 9,000 mg/L.

    FDA · DeviceRoche Diagnostics Operations, Inc.US Nationwide distribution.Official notice →
  6. US
    Drugs & medicalClass II

    TiSport, Llc recalls Permobil TiLite, Models: Aero Z, and ZRA

    Some affected wheelchairs, with transit tie downs, that are used as a passenger seat in a motor vehicle may not be configured in the right orientation to perform as intended if involved in a motor vehicle accident.…

    FDA · DeviceTiSport, LlcUS Nationwide Distribution: MD, PA, VA, IN, NY, MO, AR, NE, NJ, WA, NM, IL,…Official notice →
  7. US
    Drugs & medicalClass II

    CooperSurgical, Inc. recalls Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075-05W

    XXX

    FDA · DeviceCooperSurgical, Inc.US Nationwide Distribution Foreign: ARMENIA, BOLIVIA, CAMBODIA, CANADA, CHILE,…Official notice →
  8. US
    Drugs & medicalClass II

    CooperSurgical, Inc. recalls Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075

    Coagulate function may not operate with the use of the Hand Switch, failure of the device to coagulate tissue may lead to a prolonged procedure requiring medical intervention to control any intraoperative bleeding and…

    FDA · DeviceCooperSurgical, Inc.US Nationwide Distribution Foreign: ARMENIA, BOLIVIA, CAMBODIA, CANADA, CHILE,…Official notice →
See all drugs & medical recalls →