Drugs & medicalClass II

Windstone Medical Packaging, Inc. recalls Various Custom Surgical Instrument Disposable Kits: Part Numbers / Product Description 26000004M Custom Lasik Kit AMS10411A…

Due to Customer Convenience Kits containing 3M Steri-Drape Surgical Drapes that have been recalled by 3M Healthcare.

Read the official notice →
Date
2023-01-11
Country
United States
Brand
Windstone Medical Packaging
Product
Various Custom Surgical Instrument Disposable Kits: Part Numbers / Product Description 26000004M Custom Lasik Kit AMS10411A Nasal…
Classification
Class II
Units
Worldwide distribution - U.S. Nationwide distribution in the states of AZ, CA,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Windstone Medical Packaging recalls

  1. 2026-04-29
  2. US
    Drugs & medicalClass II

    Windstone Medical Packaging, Inc. recalls Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994

    The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space…

    FDA · DeviceWindstone Medical Packaging, Inc.US Nationwide distribution in the states of GA, OR, TN, and WA.Official notice →
  3. 2024-10-16
  4. US
    Drugs & medicalClass II

    Windstone Medical Packaging, Inc. recalls Aligned Medical Septo Pack REF AMS11480 that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a…

    Due to convenience kits containing a kit component that is under a recall action for improper use.

    FDA · DeviceWindstone Medical Packaging, Inc.U.S. Nationwide distribution in the states of CA, MO, OH, VA, and WY.Official notice →
  5. 2024-02-28
  6. US
    Drugs & medicalClass I

    Windstone Medical Packaging, Inc. recalls Aligned Medical Solutions, In House Ocular Pack, AMS12947, STERILEEO

    Sterility assurance for saline included in surgical kits cannot be guaranteed.

    FDA · DeviceWindstone Medical Packaging, Inc.US: FL, IL, CA OUS: NoneOfficial notice →
  7. 2023-05-31
  8. US
    Drugs & medicalClass II

    Windstone Medical Packaging, Inc. recalls Aligned Medical Solutions Hand Pack, REF: AmS4601E, containing P 2 Cover Light Handle Blue STE, Sterile EO

    Light handle covers may separate from the light handle (detach and fall off) during use, this could result in a procedure delay and/or impact the sterile field which could result in an injury to the patient

    FDA · DeviceWindstone Medical Packaging, Inc.US: MA OUS: NoneOfficial notice →
  9. 2022-05-25
  10. US
    Drugs & medicalClass II

    Windstone Medical Packaging, Inc. recalls Prevantics swabs and/or swabsticks contained inside the following Aligned Medical Solutions convenience kits with Name/Pack…

    Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International, that are subject to a drug recall due to uncertainty of the adequacy of the validation of the…

    FDA · DeviceWindstone Medical Packaging, Inc.US: PA, WA, FL, GAOfficial notice →
  11. 2021-11-10
  12. US
    Drugs & medicalClass I

    Windstone Medical Packaging, Inc. recalls Monoject 0.9% Sodium Chloride, Flush Prefilled Syringe, 10 mL, REF: 8881570121 inside the following Aligned Medical Solutions…

    Monoject 0.9% Sodium Chloride Flush Syringe Manufactured by Cardinal Health and placed into kits. Potential for the plunger to draw back after air has been expelled and reintroduce air back into the syringe.

    FDA · DeviceWindstone Medical Packaging, Inc.FL and PAOfficial notice →
All 13 Windstone Medical Packaging recalls →

Other drugs & medical recalls in the United States

  1. 2023-01-18
  2. US
    Drugs & medicalClass II

    RemedyRepack Inc. recalls Rifampin Capsules, 300 mg, 30 count blister card, Rx only, Mfg: Lupin Pharma, Baltimore, MD 21202, original NDC 68180-0659-07, Repackaged…

    Failed Impurities/Degradation specifications

    FDA · DrugRemedyRepack Inc.Product was distributed to one account in PA.Official notice →
  3. 2023-01-11
  4. US
    Drugs & medicalClass II

    DeRoyal Industries Inc recalls DeRoyal Tonsillectomy Tray, REF 89-10698.01

    DeRoyal is recalling certain lots of surgical procedure pack products that contain a ConMed Foot Controlled Electrosurgical Suction Coagulator. The recall is due to ConMed receiving reports that the suction ports may…

    FDA · DeviceDeRoyal Industries IncDistribution in US states of VA, and SC.Official notice →
  5. US
    Drugs & medicalClass II

    Randox Laboratories Ltd. recalls Liquid Assayed Specific Protein Control Level 2- In vitro diagnostic use, in the quality control of serum on clinical chemistry and…

    Concentration of Rheumatoid Factor has decreased in Specific Protein Control Level 1-3 causing delay in reporting results due to Quality Controls running low outside range

    FDA · DeviceRandox Laboratories Ltd.US Nationwide distribution in the states of CA, FL, OH,ME, MO, NC, NJ, PA, TN.Official notice →
  6. US
    Drugs & medicalClass II

    Altimate Medical, Inc. recalls ActiveAid 922, Shower/Commode Chair

    Device manufactured with a component with affects the foldability of the frame, not allowing it to be secured by the frame strap in the folded position.

    FDA · DeviceAltimate Medical, Inc.US Nationwide distribution in the state of Texas.Official notice →
  7. US
    Drugs & medicalClass II

    Detect Headquarters recalls Detect Covid-19 Test Product/Model Number: 21205

    There is an increased chance that the tests from affected lots may give false negative results. Health risks resulting from a false negative result include delay or lack of supportive treatment and lack of monitoring…

    FDA · DeviceDetect HeadquartersDomestic distribution nationwide. Foreign distribution to Hong Kong.Official notice →
  8. US
    Drugs & medicalClass II

    Ortho-Clinical Diagnostics, Inc. recalls VITROS Immunodiagnostic Products Intact PTH Reagent Pack- IVD For the quantitative measurement of intact parathyroid hormone…

    Lower than expected iPTH patient and Quality Control (QC) results, reported negatively biased iPTH results- an average -12% shift in patient sample results

    FDA · DeviceOrtho-Clinical Diagnostics, Inc.Worldwide distribution - US Nationwide and the countries of Australia,…Official notice →
See all drugs & medical recalls →