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.
Read the official notice →- Date
- 2025-04-02
- Country
- United States
- Brand
- CooperVision
- Product
- Brand Names: MyDay Toric, LensCrafters One Day Premium Daily Disposable Contact Lenses For Astigmatism, Pearle Vision 1 Day Premium For…
- Classification
- Class II
- Units
- Domestic: CA, CO, FL, IL, KY, MI, NC, NE, NJ, NY, OH, OR, UT, VA, WA.…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2026-09-30
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A small number of lenses within the affected lot are of the incorrect power.
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CooperVision, 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
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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 → - 2024-10-09
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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
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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
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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
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Other drugs & medical recalls in the United States
- 2025-04-02
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Baxter Healthcare Corporation recalls Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated with immobility,…
The air bladders inside the mattress may move out of position when the head of the bed is elevated, causing a dip in the mattress.
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Checkpoint Surgical Inc recalls Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint Guardian Intraoperative Lead, Small Model/Catalog Number:…
Adhesive on the back of the lead may not fully encapsulate the metallic portion of the wire and button subassembly, potentially leading to exposed metal. There is a risk of electrical current leakage, which may lead to…
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MEDLINE INDUSTRIES, LP - Northfield recalls Medline ReNewal Reprocessed Livewire Steerable Electrophysiology Catheters, Medline Item Numbers: 401582R, 401904R, 401904R,…
Devices may have higher than expected amounts of bacterial endotoxin.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the states of AR, AZ, CA, CO, IA, IL, KS, OR,…Official notice → - US
Microbiologics Inc recalls Helix Elite Inactivated Standard: Inactivated Influenza A/B and Respiratory Syncytial Virus, Multi-analyte, unassayed quality control…
The RSV target may give a late Ct value and could potentially not pass QC.
FDA · DeviceMicrobiologics IncWorldwide - US Nationwide distribution in the states of KY, MT, NJ, NY, WI and…Official notice → - US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits labeled as: 1) C SCOPE DISPOSABLE KIT, Pack Number 613034700, 2) C SCOPE DISPOSABLE KIT, Pack Number…
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
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Merit Medical Systems, Inc. recalls Prelude IDEAL 4 F Hydrophilic Sheath Introducer, REF: PID4F16021PW/D
Hydrophilic Sheath Introducer labeled for 4F dilators may instead incorrectly contain 5F dilators. Incorrect dilator use may result in procedure delay.
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