Drugs & medicalClass II

Boston Foundation For Sight recalls BostonSight SCLERAL Lens

Select orders of lenses were manufactured with errors impacting sagittal height, haptics, or both.

Read the official notice →
Date
2025-08-06
Country
United States
Brand
Boston Foundation For Sight
Product
BostonSight SCLERAL Lens
Classification
Class II
Units
Worldwide distribution - US Nationwide and the countries of Canada.
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2025-08-06
  2. US
    Drugs & medicalClass II

    Microbiologics Inc recalls LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as: 1) REF 0894K (6-pack), 2) REF 0894P (2-pack)

    KWIK-STIK REF numbers: 0894P, 0894K and LYFO DISK" 0894L may result in failure to recover the target microorganism. All lots of REF 894-76 are impacted.

    FDA · DeviceMicrobiologics IncWorldwide distribution - US Nationwide and the countries of France, Colombia,…Official notice →
  3. US
    Drugs & medicalClass II

    Maquet Cardiopulmonary Gmbh recalls Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold 2 x 2 kg infusion bags.

    Device does not comply with the labeling requirements of international standard IEC 60601-1.

    FDA · DeviceMaquet Cardiopulmonary GmbhWorldwide distribution - US Nationwide and the countries of Australia, New…Official notice →
  4. US
    Drugs & medicalClass II

    Phasor Health, LLC recalls Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35

    Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.

    FDA · DevicePhasor Health, LLCUS: PA, IN, AZ, MO, LA, FL, TX, MA, OH, TN, MI, WV, VA, CA, DE, NH, GA, SC,…Official notice →
  5. US
    Drugs & medicalClass II

    PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Allura R8.2.x Systems. Software Verion: R8.2.x. 1. Allura Xper FD10, Model Number: 722026. 2. Allura Xper…

    Potential for temporary loss of imaging (X-ray) functionality due to software issue.

    FDA · DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Worldwide - US Nationwide and the countries of Algeria, Argentina, Australia,…Official notice →
  6. US
    Drugs & medicalClass II

    MICROVENTION INC. recalls LIFEPEARL Drug Elutable Microspheres: 200 +/- 50 micrometers, REF: 8LP2S200; 400 +/- 50 micrometers, REF: 8LP2S400

    Drug Elutable Microspheres have a smaller actual average diameter that is not within specification, which may lead to inability to reach the desired treatment location (non-targeted embolization), additional…

    FDA · DeviceMICROVENTION INC.OUS: Italy, Spain, Portugal, Poland, Belgium, Germany, Denmark, France,…Official notice →
  7. US
    Drugs & medicalClass II

    Steris Corporation recalls Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR E-Series Surgical Lighting Systems

    The DFPM yoke assembly ("yoke assembly") may detach from the spring arm. Should the yoke assembly detach from the spring arm, the yoke assembly would not be expected to fully detach but rather hang from the wiring…

    FDA · DeviceSteris CorporationWorldwide - US Nationwide and Puerto Rico and the country of Canada.Official notice →
See all drugs & medical recalls →