Recall Atlas
Drugs & medicalClass II

Linkbio Corp. recalls LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 7MM X 58MM Item Number: 15-2028/13

Additional Label Warnings: Amendment / reinforcement of the Surgical Technique and future product training on the updated technique, due to early aseptic loosening or increased wear of the implant caused by suboptimal…

Read the official notice →
Date
2023-05-10
Country
United States
Brand
Linkbio
Product
LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 7MM X 58MM Item Number: 15-2028/13
Classification
Class II
Units
NY, NV Foreign: Bulgaria, France, Italy, Norway, Poland, Sweden, Switzerland,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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

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  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 Linkbio recalls

  1. 2026-04-22
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    Linkbio Corp. recalls LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.

    The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.

    FDA · DeviceLinkbio Corp.US Nationwide distribution in the state of Alabama, Florida, and Kansas.Official notice →
  3. 2023-06-07
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    Linkbio Corp. recalls LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6 Tilastan, cemented. Intended for primary and revision…

    Contains the incorrect implant in the packaging. The packaging incorrectly contains the opposite side of the implant (Lateral-Right/Medial-Left instead of Medial-Right/Lateral-Left).

    FDA · DeviceLinkbio Corp.US Nationwide Distribution - AL, GA, IL, IN, LA, NV, TXOfficial notice →
All 3 Linkbio recalls →

Other drugs & medical recalls in the United States

  1. 2023-05-10
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    Firmware versions have the potential to mis-associate sample IDs leading to incorrect results or delayed sodium, potassium, and chloride patient results. Falsely increased or decreased electrolytes can lead to either…

    FDA · DeviceInpeco S.A.Worldwide distribution - US Nationwide and the countries of ARGENTINA,…Official notice →
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    DeVilbiss Healthcare LLC recalls DEVILBISS HEALTHCARE 1025 SERIES OXYGEN CONCENTRATOR, Model Numbers 1025DS, 1025UK, 1025KS, and 1025KS-AR

    The instruction manual is being replaced with an updated version that is in alignment with labeling requirements specified in the IEC-60101-1 standard.

    FDA · DeviceDeVilbiss Healthcare LLCWorldwide - US Nationwide distribution.Official notice →
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    MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip Pack Caps on VITROS¿ 5600 and XT 7600 Integrated Systems, results may be delayed results if a pack becomes unusable

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    DermLite LLC recalls DERMLITE DL4W, REF: DL4W, Rx Only MD, CE

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    FDA · DeviceDermLite LLCWorldwide - US Nationwide distribution in the states of CA, AZ, TX, FL, NE,…Official notice →
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    There is a negative bias with urine patient samples and urine cortisol Quality Control (QC) results intermittently out of range low.

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    Spacelabs Healthcare, Inc. recalls Ultraview SL (UVSL) Command Module, Model 91496

    Command modules will display the following when parameter processing is suspended, depending on software version: 1) Older versions will have waveforms present with no alarms, 2) Newer versions have waveforms absent…

    FDA · DeviceSpacelabs Healthcare, Inc.US Nationwide distribution in the states of SD, KY, MO, WA, OH, NC, CA, OR,…Official notice →
See all drugs & medical recalls →