Drugs & medicalClass II

Mirion Technologies (Capintec), Inc. recalls Captus 4000e Thyroid Uptake System, Models: 1. 5430-30151, 2. 5430-30152, 3. 5430-30154;

Potential for failure of the tension bolt which would allow the spring arm to unexpectedly fall to its lowest position, which is approximately 25 inches (63.5 cm) from the ground.

Read the official notice →
Date
2026-09-23
Country
United States
Brand
Mirion Technologies
Product
Captus 4000e Thyroid Uptake System, Models: 1. 5430-30151, 2. 5430-30152, 3. 5430-30154;
Classification
Class II
Units
Worldwide distribution - US Nationwide and the countries of ALGERIA, AUSTRIA,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Mirion Technologies recalls

  1. 2024-06-05
  2. US
    Drugs & medicalClass II

    Mirion Technologies (Capintec), Inc. recalls Captus 4000e Thyroid Uptake System. Intended to be used to perform Thyroid Uptakes, Staff Bioassay, and wipe tests.

    Complaints of unexpected detachment of the collimator have been reported.

    FDA · DeviceMirion Technologies (Capintec), Inc.Worldwide - US Nationwide distribution and the countries of ALGERIA,…Official notice →
  3. 2024-02-21
  4. US
    Drugs & medicalClass II

    Mirion Technologies (Capintec), Inc. recalls Captus 4000e Thyroid Uptake Systems- Intended to be used by trained Nuclear Medicine Technologists or Nuclear Medicine…

    Spring arm failure with Captus 4000e Thyroid Uptake Systems, can cause the collimator to fall downward to its lowest point of travel, causing potential injury with a patient or operator

    FDA · DeviceMirion Technologies (Capintec), Inc.Nationwide Foreign: AUSTRIA BANGLADESH BRASIL Brazil CANADA CHILE Costa Rica…Official notice →
All 3 Mirion Technologies recalls →

Other drugs & medical recalls in the United States

  1. 2026-09-23
  2. US
    Drugs & medicalClass II

    F & A Foundation recalls Reign Medical Clench Staple System (Compression), Description/REF: 9mm x 7mm/152-30907; 11mm x 10mm/152-31110; 15mm x 12mm/152-31512; 18mm…

    Bone fixation staple requires a new 510(k); the performance characteristics of this device have not been adequately established.

    FDA · DeviceF & A FoundationUS Nationwide distribution in the states of TX, OK, MD, VT, MA, LA.Official notice →
  3. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A

    Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.

    FDA · DeviceMedline Industries, LPUS Nationwide distribution in states of Arkansas, Florida, North Carolina,…Official notice →
  4. US
    Drugs & medicalClass II

    Howmedica Osteonics Corp. recalls SCORPIO C-DOME PATELLA 73-2710 73-2910 SCORPIO U-DOME PATELLA 73-3110 73-3508 73-3708 73-3710 73-3910 Orthopaedic implant components…

    Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in…

    FDA · DeviceHowmedica Osteonics Corp.Worldwide distribution - US Nationwide and the countries of Canada, LATAM,…Official notice →
  5. US
    Drugs & medicalClass II

    Datex-Ohmeda, Inc. recalls Aisys CS2 with Et Control, Datex-Ohmeda anesthesia system, Part Number 1011-9000-000

    Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 100% O2 to the breathing system enabling…

    FDA · DeviceDatex-Ohmeda, Inc.Worldwide - US Nationwide distribution.Official notice →
  6. US
    Drugs & medicalClass II

    Boston Scientific Corporation recalls Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adaptor, (1)DVI Cable, (1) DVI to…

    A subset of power adapters used with the connect console may exhibit higher-than-expected resistance in the electrical grounding path. As a result, the power adaptor may fail electrical safety testing during…

    FDA · DeviceBoston Scientific CorporationWorldwide - US Nationwide distribution including in the states of AZ, FL, CA,…Official notice →
  7. US
    Drugs & medicalClass II

    Stryker Sustainability Solutions recalls REF:2B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW TECHNOLOGY & SLEEVE 5MM X 75MM

    Reusable access port system may crack or seperate during use.

    FDA · DeviceStryker Sustainability SolutionsUS Nationwide distribution including in the states of Alabama, Alaska,…Official notice →
See all drugs & medical recalls →