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  2. A Full List of Recalled Eye Drops Linked to Potential ... - AOL

    www.aol.com/full-list-recalled-eye-drops...

    This recall includes over 700,000 bottles with expiration dates reaching into late 2023 and early 2024 in the following lots: Lot 114349, Lot 117396, Lot 0120128, Lot 114371, and Lot 123781.

  3. Over 27 Eye Drops Have Been Recalled: What You Need to Know - AOL

    www.aol.com/lifestyle/eye-drop-recall-know...

    Eye drops are being recalled due to a rare bacterium found in artificial tears. Find a list of recalled drops in 2023. Plus, eye infection symptoms.

  4. Recent recalls, FDA warnings about eye care products are ...

    www.aol.com/lifestyle/recent-recalls-fda...

    The latest recalls and warnings underscore the need to properly vet your eye drops and other eye care products, say experts. Recent recalls, FDA warnings about eye care products are concerning ...

  5. Alcon - Wikipedia

    en.wikipedia.org/wiki/Alcon

    Alcon offices in Johns Creek, Georgia. Alcon Inc. (German: Alcon AG) is a Swiss-American pharmaceutical and medical device company specializing in eye care products. It has a paper headquarters in Geneva, Switzerland but its operational headquarters are in Fort Worth, Texas, United States, where it employs about 4,500 people.

  6. List of withdrawn drugs - Wikipedia

    en.wikipedia.org/wiki/List_of_withdrawn_drugs

    This list is not limited to drugs that were ever approved by the FDA. Some of them (lumiracoxib, rimonabant, tolrestat, ximelagatran and ximelidine, for example) were approved to be marketed in Europe but had not yet been approved for marketing in the US, when side effects became clear and their developers pulled them from the market.

  7. FDA recall policies - Wikipedia

    en.wikipedia.org/wiki/FDA_recall_policies

    FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.

  8. The latest eye medicine to be recalled: 715,000 bottles of ...

    www.aol.com/latest-eye-medicine-recalled-715...

    The FDA posting of the recall says Teva’s pulling Clear Eyes, Once Daily, Eye Allergy Itch Relief drops for a failed impurities test. This covers the 715,682 bottles in lot Nos. 114349 ...

  9. More eye medicine recalled in 13-state outbreak of ‘drug ...

    www.aol.com/news/more-eye-medicine-recalled-13...

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