Recall Atlas
Drugs & medicalClass II

Uoc Usa Inc recalls United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part, RHS, 25 mm Length, Catalog # 2915-1025

Due to product not meeting specification for concentricity and failing to meet requirements of dynamic fatigue testing.

Read the official notice →
Date
2021-10-20
Country
United States
Brand
Uoc Usa Inc
Product
United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part, RHS, 25 mm Length, Catalog # 2915-1025
Classification
Class II
Units
U.S. Nationwide: CA, CO, and NV No O.U.S.
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2021-10-20
  2. US
    Drugs & medicalClass II

    Elekta, Inc. recalls Elekta Medical Linear Accelerator (EMLA), configured as follows: a. Elekta Precise Digital Accelerator; b. Elekta Harmony; c. Elekta…

    There is a risk that the Diode D1 in the Modulator can fail in a destructive manner when removed from the machine, and that the protective tube surrounding the diode may fail to contain the ejected matter.

    FDA · DeviceElekta, Inc.Distributed nationwide to FL, NC, OH, CA, IL, MD, OR, AL, NY, PA, MA, AK, GA,…Official notice →
  3. US
    Drugs & medicalClass II

    ELEKTA SOLUTIONS AB recalls Elekta Medical Linear Accelerator (EMLA): Elekta Harmony Pro, REF 1555143; Elekta Infinity, REF 1552091, and Elekta Versa HD, REF 1552093.

    There is a risk that the Diode D1 in the Modulator can fail in a destructive manner when removed from the machine, and that the protective tube surrounding the diode may fail to contain the ejected matter.

    FDA · DeviceELEKTA SOLUTIONS ABDistribution was to ND and NC. There was no military/government distribution.Official notice →
  4. US
    Drugs & medicalClass II

    Flower Orthopedics Corporation recalls Flower Drill Bit Kit 2.0 mm - intended to be used with solid 2.0mm screws and can be used with any plate that has been cleared as…

    Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure

    FDA · DeviceFlower Orthopedics CorporationArizona California Colorado Florida Florida Illinois Indiana Nevada Ohio Texas…Official notice →
  5. US
    Drugs & medicalClass II

    Draeger Medical, Inc. recalls Babylog VN500 Ventilator with Installed CO2 Measurement Option-intended for the ventilation of neonatal patients from 0.4 kg (0.88 lbs) up…

    Software 2.51 and Lower with Installed CO2 Measurement Option, may result in Restart of the Ventilator, brief cessation of ventilation can occur and loss of PEEP for approx. 8 seconds

    FDA · DeviceDraeger Medical, Inc.US NationwideOfficial notice →
  6. US
    Drugs & medicalClass II

    Intuitive Surgical, Inc. recalls Ion Flexison Biopsy Needle, 19G, Extension Range : 0-3 cm, Ref: 490104-09 and 49004-10, 5-pack, Sterile EO, Rx only, UDI:00886874115978

    Potential for the sheath tip on the biopsy needle to separate from the sheath shaft.

    FDA · DeviceIntuitive Surgical, Inc.US: AZ, AR, CA, CO, DC, FL, GA, IL, IN, IO, MD, MA, MI, MN, MO, NV, NJ, NY,…Official notice →
  7. US
    Drugs & medicalClass II

    Centese Inc. recalls Thoraguard Chest Tube Kit, 20 Fr

    An adhesive joint in the SmartValve component of the device can become compromised resulting in a leak.

    FDA · DeviceCentese Inc.Distribution to a single consignee located in California.Official notice →
See all drugs & medical recalls →