CooperVision, Inc. recalls Biofinity XR Toric Contact Lens
Lens blisters may have an incomplete or leaking seal which may render them unsterile.
Read the official notice →- Date
- 2025-07-30
- Country
- United States
- Brand
- CooperVision
- Product
- Biofinity XR Toric Contact Lens
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the countries of Brazil, 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 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
USCooperVision, 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.
FDA · DeviceCooperVision, Inc.US Nationwide distribution in the states of MN, OH, WI.Official notice →- 2025-10-01
- US
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 → - 2025-04-02
- 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
- 2025-08-06
- US
Lupin Pharmaceuticals Inc. recalls Amlodipine and Benazepril HCl Capsules USP 2.5 mg/10 mg, 100 Capsules bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc.,…
Labeling: Incorrect or Missing Lot and/or Exp Date: released with wrong expiry date as Feb.2027 instead of Jan.2027
- 2025-07-30
- US
Stryker Corporation recalls Stryker, StrykeFlow REF: 0250070520 / 2, Disposable Suction/Irrigator with Disposable Tip
Due to complaints their is the potential that irrigation solution may leaked into the handpiece and battery pack causing it to malfunction.
FDA · DeviceStryker CorporationWorldwide - US Nationwide distribution including in the states of Alabama,…Official notice → - US
Medtronic, Inc. recalls Medtronic CareLink SmartSync Patient Connector, Model Number 24967 with the following software components: 1. Cobalt Crome application,…
In prior SmartSync application versions, the Abort button stopped the test that was selected. During an induction test, there was a limited window of time for the user to abort a therapy, thereby limiting the user's…
- US
Johnson & Johnson Vision Care, Inc. recalls ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
Due to defects (bubbles/voids) identified during standard finished goods testing
FDA · DeviceJohnson & Johnson Vision Care, Inc.Worldwide - U.S. Nationwide distribution including in the states of AL, AZ,…Official notice → - US
Becton Dickinson & Co. recalls BD COR System Software. Model Number: 444829.
Potential for functionality issue that supports the Over labeling feature and could lead to possible false negative results.
FDA · DeviceBecton Dickinson & Co.Worldwide - US Nationwide distribution in the states of Florida, Texas and…Official notice → - US
Bridge to Life Ltd recalls Bridge to Life EasiSlush, (Sodium Chloride Solution for Sterile Slush Preparation) (0.9% Sodium Chloride Irrigation, USP), Part Number REF…
The firm issued a field safety notice after becoming aware of three lots of products not having quarterly dose audits being completed on time in the first quarter of 2024. Routine lot by lot testing was completed…
FDA · DeviceBridge to Life LtdUnited States - New York, Maryland, Alabama, North Carolina, South Carolina,…Official notice →