Recall : more meds from McNeil Consumer Healthcare

The FDA just announced there are now even more recalled items from McNeil Consumer Healthcare. This is the same recall that is going on due to some heavily-stinkified packaging that is making a lot of people sick.

The current recall list is below…

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FULL RECALLED PRODUCT LIST:

Product Name Lot Number UPC Code
BENADRYL® ALLERGY ULTRATAB™
BENADRYL® ALLERGY ULTRATAB™ TABLETS  100 count ABA567 312547170338
BENADRYL® ALLERGY ULTRATAB™ TABLETS 100 count ABA574 312547170338
Children’s TYLENOL® Meltaways
CHILDREN’S TYLENOL® MELTAWAYS BUBBLEGUM  30 count ABA544 300450519306
MOTRIN® IB
MOTRIN® IB CAPLET 24 count ACA003 300450481030
MOTRIN® IB CAPLET bonus pack 50+25 count ACA002 300450481764
MOTRIN® IB TABLET 100 count AFA060 300450463043
TYLENOL®, Extra Strength
TYLENOL®, Extra Strength  EZ TABLET 225 count ASA206 300450422378
TYLENOL®, Extra Strength  EZ TABLET 50 count ABA005 300450422507
TYLENOL®, Extra Strength  COOL CAPLET 24 count ABA566 300450444240
TYLENOL®, Extra Strength  CAPLET bonus pack 24+12 count ACA025 300450444318
TYLENOL®, Extra Strength  CAPLET 50 count AFA018 300450449078
TYLENOL®, Extra Strength  CAPLET 50 count

(included in Day/Night Pack)

ABA168 300450444530
TYLENOL®, Day & Night Value Pack

(contains Extra Strength CAPLET 50 count Lot # ABA168 & UPC  300450444530)

AEC005 300450527103
TYLENOL®, Day & Night Value Pack

(contains Extra Strength CAPLET 50 count Lot # ABA168 & UPC  300450444530)

AFC005 300450527103
TYLENOL®, Day & Night Value Pack

(contains Extra Strength CAPLET 50 count Lot # ABA168 & UPC  300450444530)

ADC002 300450527103
TYLENOL®, Extra Strength RAPID RELEASE GELCAP 24 count ACA024 300450488244
TYLENOL®, Extra Strength RAPID RELEASE GELCAP 225 count AJA119 300450488251
TYLENOL® PM
TYLENOL® PM CAPLET 24 count ACA005 300450482242
TYLENOL® PM CAPLET 24 count ADA259 300450482242
TYLENOL® PM GELTAB 50 count AFA100 300450176509
TYLENOL® PM RAPID RELEASE GELCAP 20 count ACA004 300450244208

Chunk ’em if you got ’em.

Here’s the link to the official FDA recall article.