Recall archive
13 recalls · page 1 of 1
Reported Nov 16, 2016
Transderm Scop (scopolamine) Transdermal System, 1.5 mg, 24 patches Multi pack, Rx only, Marketed by Baxter Healthcare…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sandoz Inc.
Matched: Product · Product details — Defective Delivery System; reports of damaged product that may alter the predicted release of scopolamine following transdermal application.
FDA (openFDA drug enforcement)
Reported Mar 5, 2014
Benefiber fiber supplement stick packs, sugar free and taste free, packaged in the following configurations: (1)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novartis Consumer Health
Matched: Brand · Product details — The products are being recalled due to the receipt of a relatively high number of consumer complaints.
FDA (openFDA food enforcement)
Reported Jan 29, 2014
Theraflu Flu & Sore Throat (acetaminophen 650 mg, pheniramine maleate 20 mg, phenylephrine hydrochloride 10 mg) powder…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novartis Consumer Health
Matched: Brand · Product details — Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
15 more products in this recall
FDA (openFDA drug enforcement)
Reported Jan 22, 2014
Maximum Strength Comtrex Day/Night Cold & Cough, Acetaminophen 325mg, Chlorpheniramine Maleate 2mg, Dextromethorphan…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Novartis Consumer Health
Matched: Brand · Product details — Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.
6 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 4, 2013
Loratadine, USP 10 mg, Antihistamine, packaged in blister packs. All manufactured by Novartis Consumer Health, Inc,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Novartis Consumer Health
Matched: Brand · Product · Product details — Failed Tablet/Capsule Specifications: The products are being recalled due to chipped and broken tablets.
FDA (openFDA drug enforcement)
Reported Oct 9, 2013
Benefiber Fiber Supplement, Orange Natural Flavor, Non-Thickening Powder, Sugar Free, packaged in 5.7-oz. (35 servings)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novartis Consumer Health
Matched: Brand · Product details — The products are being recalled due to the receipt of a relatively high number of consumer complaints.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 25, 2013
Benefiber, Fiber plus Calcium Supplement, Wild Berry Chewables 90ct, sugar free, chewable tablets bottle. Novartis…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Novartis Consumer Health
Matched: Brand · Product · Product details — The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 28, 2013
Maalox Extra Strength Antacid with Anti-Gas (calcium carbonate and simethicone) chewable tablets, 1000 mg/60 mg,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Novartis Consumer Health
Matched: Brand · Product details — Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
8 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 14, 2013
Excedrin Extra Strength (Acetaminophen 250 mg, Aspirin (NSAID) 250 mg and Caffeine 65 mg), a) 2-ct tablets in pouches…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novartis Consumer Health
Matched: Brand · Product details — Defective container: products are packaged in pouches which may not have been fully sealed
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Jun 12, 2013
Novartis Lamisil AT Cream, Terbinafine Hydrochloride Cream 1% Antifungal, Novartis Consumer Health, Inc., Parsippany,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Novartis Consumer Health
Matched: Brand · Product · Product details — Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot.
4 more products in this recall
FDA (openFDA drug enforcement)
Reported May 29, 2013
Lamisil AT (terbinafine hydrochloride cream 1% antifungal), 24 g (.85 oz) tube, Novartis Consumer Health, Parsippany,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Novartis Consumer Health
Matched: Brand · Product · Product details — Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot.
FDA (openFDA drug enforcement)
Reported May 8, 2013
Percocet 10/325 mg tablets, 100-count tablets per bottle, Rx only, Dist. By: Physicians Total Care, Tulsa, OK 74146;…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Physicians Total Care, Inc.
Matched: Product details — Presence of Foreign Tablets/Capsules: One bottle of Percocet 10/325 mg was found to contain a tablet of Endocet 10/25 mg, the generic form.
FDA (openFDA drug enforcement)
Reported Mar 27, 2013
Myoflex (trolamine salicylate) 10%, Pain Relieving Cream, a) 2-oz tube, b) 4-oz. tube, OTC. The firm name on the label…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Novartis Consumer Health
Matched: Brand · Product details — Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or expiration date may be illegible.
4 more products in this recall
FDA (openFDA drug enforcement)
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