CooperVision, Inc. recalls Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day
A small number of lenses within the affected lot are of the incorrect power.
Read the official notice →- Date
- 2026-09-30
- Country
- United States
- Brand
- CooperVision
- Product
- Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day
- Classification
- Class II
- Units
- US Nationwide distribution in the states of MN, OH, WI.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- 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 CooperVision recalls
- 2025-10-01
USCooperVision, Inc. recalls MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 54% water content, Toric, cast moulded Silicone Hydrogel,…
One lot manufactured with an invalid sterilization cycle.
FDA · DeviceCooperVision, Inc.US Nationwide distribution in the states of Florida, Kentucky, North Carolina,…Official notice →- 2025-07-30
- US
CooperVision, Inc. recalls Biofinity XR Toric Contact Lens
Lens blisters may have an incomplete or leaking seal which may render them unsterile.
FDA · DeviceCooperVision, Inc.Worldwide distribution - US Nationwide and the countries of Brazil, Canada,…Official notice → - 2025-04-02
- US
CooperVision, Inc. recalls Brand Names: MyDay Toric, LensCrafters One Day Premium Daily Disposable Contact Lenses For Astigmatism, Pearle Vision 1 Day Premium For…
a limited number of lots were manufactured with an incorrect cylinder power.
FDA · DeviceCooperVision, Inc.Domestic: CA, CO, FL, IL, KY, MI, NC, NE, NJ, NY, OH, OR, UT, VA, WA.…Official notice → - 2024-10-09
- US
CooperVision, Inc. recalls Biofinity Toric Multifocal Lenses - Soft Contact lenses Indicated for the correction of ametropia (myopia or hyperopia with astigmatism)…
Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity
FDA · DeviceCooperVision, Inc.Worldwide distribution - US Nationwide and the country of Canada.Official notice → - 2023-03-29
- US
CooperVision, Inc. recalls Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90
The lenses manufactured in the affected lot were made with a misaligned axis resulting in lenses with the incorrect power.
FDA · DeviceCooperVision, Inc.Worldwide - US Nationwide distribution in the states of FL, IL, NY, UT, and…Official notice → - 2023-03-08
- US
CooperVision, Inc. recalls Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended wear)
Manufactured with misaligned axis resulting in lenses with the incorrect power, users may experience poor visual acuity
FDA · DeviceCooperVision, Inc.US Nationwide distribution in the states of CA, OH, NC, PA.Official notice →
Other drugs & medical recalls in the United States
- 2026-09-30
- US
Abiomed, Inc. recalls Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1. Impella Controller, Packaged,…
Retrospective report of issues remedied in 2019 with firmware and software patches: 1. Defects in optical bench (OPB) firmware V2.19, which affected the accuracy and stability of the pressure signal the AIC system…
FDA · DeviceAbiomed, Inc.Worldwide - US Nationwide and the countries of Austria, Belgium, Canada,…Official notice → - US
Becton, Dickinson and Company recalls ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The non-invasive ForeSight oximeter cable is…
Due to incorrect switching of Channel 1 and 2 on the module and flag labels on the tissue oximetry cables.
FDA · DeviceBecton, Dickinson and CompanyWorldwide - U.S Nationwide distribution including in the states of AK, AL, AR,…Official notice → - US
Philips Ultrasound, LLC recalls Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234
Due to software issue with ultrasound system, doppler sample is displayed shallower than its actual measurement location, potentially causing inaccurate blood flow velocity measurements and misdiagnosis.
FDA · DevicePhilips Ultrasound, LLCWorldwide - US Nationwide distribution in the states of AL, CA, CT, FL, GA,…Official notice → - US
Olympus Corporation of the Americas recalls Olympus BiCOAG Hemostasis Probe 7Fr Fixed Pin Connector. Model/Catalog Number: CD-B622LA.
Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.
FDA · DeviceOlympus Corporation of the AmericasWorldwide distribution - US Nationwide and the countries of Canada, Latin…Official notice → - US
Philips North America Llc recalls Achieva 3.0T; Model Numbers (REF): 1. 781177, 2. 781277, 3. 781278, 4. 781344, 5. 781345;
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.
FDA · DevicePhilips North America LlcWorldwide distribution - US Nationwide and the countries of Albania, Algeria,…Official notice → - US
Biomerieux Inc recalls VITEK 2 AST-N461 TEST KIT, GRAM NEGATIVE SUSCEPTIBILITY TESTING - AUTOMATED, Reference Number 424811
The issue is related to card pouch damage associated with a portion of the lot which was produced on a specific card pouching device, in a specific timeframe, causing a potential risk of false resistant results. False…
FDA · DeviceBiomerieux IncInternational distribution to the countries of Austria, Germany, Luxembourg.Official notice →