Drugs & medicalClass II

Mentor Texas, LP. recalls Artoura Breast Tissue Expanders Reference Numbers: TEXP110RH TEXP120RH TEXP120RUH TEXP130RH TEXP135RH TEXP140RH TEXP150RH Textured, High &…

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Read the official notice →
Date
2026-04-08
Country
United States
Brand
Mentor Texas
Product
Artoura Breast Tissue Expanders Reference Numbers: TEXP110RH TEXP120RH TEXP120RUH TEXP130RH TEXP135RH TEXP140RH TEXP150RH Textured, High &…
Classification
Class II
Units
Worldwide distribution - US Nationwide and the countries of Canada, Albania,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

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Other drugs & medical recalls in the United States

  1. 2026-04-08
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    Ultradent Products, Inc. recalls Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011.

    Composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment.

    FDA · DeviceUltradent Products, Inc.US: MA, WI, ME, AL, NY, MN, CA, KY, IL, WY, WA, OH, PR, CT, OR, NJ, MI, NC,…Official notice →
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    Stryker Communications recalls Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001

    Surgical light assembly may not adequate support the weight of the ceiling cover.

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    PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013;

    Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

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    BD KIESTRA LAB AUTOMATION recalls BD Kiestra" ReadA; Catalog No.: 446948.

    In certain situations, following a system reboot, one or more modules may have become unreachable via the remote connectivity interface. When this occurred, there was potential for delays in plate retrieval from the…

    FDA · DeviceBD KIESTRA LAB AUTOMATIONDomestic: KS, MD, MN, NJ, TX, VA; International: Australia, Austria, Belgium,…Official notice →
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    Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Enzymatic Hemoglobin A1c (A1c_E); Siemens Material Number (SMN): 11097536;

    A potential for depressed results for Atellica CH A1c_E when processing Atellica CH RCRP on the same analyzer. Customers processing A1c_E and RCRP on separate analyzers are not impacted by the recall. The frequency and…

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