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McNeil Consumer Healthcare Announces a Voluntary Nationwide Recall of All Lots of TYLENOL(R) Arthritis Pain 100 Count With EZ-OPEN CAP
Date:12/18/2009

should contact their healthcare provider. Any adverse reactions may also be reported to the FDA's MedWatch Program by fax at 1-800-FDA-0178, by mail at MedWatch, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch website at www.fda.gov/medwatch.

The affected TYLENOL® Arthritis Pain Caplet 100 count product lot numbers can be found on the side of the bottle label. See the full list of affected product lot numbers below:

Recalled Product- Full List: http://www.tylenol.com/page2.jhtml?id=tylenol/news/subp_tar_recall.inc


                                                                 Product
    UPC #   NDC Code #                  Lot #                  Description
    -----   ----------               ---------                 -----------
    0045-    8382100  07CMC011, 07DMC022, 07DMC024, 07FMC032, TYLENOL(R)
     0838-21          07FMC033, 07GMC038, 07GMC039, 07HMC045, ARTHRITIS PAIN
                      07HMC051, 07HMC053, 07JMC064, 07JMC069, CAPLET 100 COUNT
                      07JMC070, 07JMC071, 07XMC055, 07XMC058, BOTTLES (with
                      07XMC062, 08AMC002, 08AMC005, 08CMC026, red EZ-OPEN CAP)
                      08DMC029, 08EMC037, 08EMC039, 08FMC044,
                      08FMC045, 08GMC050, 08GMC053, 08GMC063,
                      08GMC065, 08JMC103, 08JMC109, 08JMC110,
                      08JMC111, 08KMC124, 08KMC127, 08KMC131,
                      08KMC132, 08XMC093, 08XMC094, 08XMC095,
 
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SOURCE  McNeil Consumer Healthcare
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