Labeling and dosing error recalls
Nothing is contaminated in these recalls — the package says the wrong thing. That can mean a bottle holding a different strength than the label states, two products packed in the wrong carton, or missing directions. For medication these can matter as much as contamination, because the dose taken is the wrong one.
983 stored notices, reported between Jun 20, 2012 and Nov 11, 2026. Newest first.
Reported Dec 8, 2021
Tydemy (drospirenone, ethinyl estradiol & levomefolate calcium tablets, 3 mg/0.03 mg/0.451 mg and levomefolate calcium…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lupin Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Nov 24, 2021
Flocinolone Acetonide 0.01% Topical Oil, Body Oil, Rx, packaged in 4 oz. bottle, Distributed by: Amneal Pharmaceuticals…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amneal Pharmaceuticals
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 10, 2021
The MEDRAD Twist & Go Disposable Syringe 150 mL with Quick Fill Tube is a syringe made from a clear polycarbonate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer Medical Care, Inc.
FDA (openFDA device enforcement)
Reported Nov 10, 2021
GM Helix Acqua Implant 3.5x10, Article No. 140.944
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jjgc Industria E Comercio De Materials Dentarios Sa
FDA (openFDA device enforcement)
Reported Oct 27, 2021
AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation Powder, Sample Not For Sale,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
4 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 20, 2021
Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection, 1 mg per vial; Diluent for Glucagon, 1 mL syringe.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eli Lilly & Company
FDA (openFDA drug enforcement)
Reported Oct 20, 2021
Heparin, GORE VIABAHN VBX, BALLOON EXPANDABLE ENDOPROTHESIS, REF BXAL085902E, 8 MM X 59 MM 8 Fr, LARGE BALLOON…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W L Gore & Associates, Inc.
FDA (openFDA device enforcement)
Reported Oct 6, 2021
Xcela PICC with PASV Valve Technology/Kit 5 F-55cm; (Maximum Flow Rate 3.5 mL/Sec)-indicated for short or long-term…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics Inc. (Navilyst Medical Inc.)
FDA (openFDA device enforcement)
Reported Oct 6, 2021
Daytime Severe Cold & Flu Relief 8 Pre-Measured Vials 0.51 FL OZ (15 mL) Each 4.06 FL OZ (120 mL) Total/Nighttime…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.New Vision Pharmaceuticals LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 29, 2021
Betadine Solution Swabstick Povidone-Iodine Solution USP, 10 % single and three count Antispetic Non-Sterile Solution…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avrio Health L.p
FDA (openFDA drug enforcement)
Reported Sep 22, 2021
Lidocaine Hydrochloride Topical Solution, USP, 4% , 50 mL glass bottles, Rx Only, Teligent Pharma Inc. Buena, New…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Teligent Pharma, Inc.
FDA (openFDA drug enforcement)
Reported Sep 22, 2021
Kroger 70% Isopropyl Alcohol First Aid Antiseptic 32 FL OZ (1 QT) 946 mL 5 Dist. By The Kroger Co., Cincinnati, Ohio…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vi-Jon, Inc.
FDA (openFDA drug enforcement)
Reported Sep 15, 2021
QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)), 16.9 FL OZ (500 ML) bottles, Manufactured by: Guangzhou Minghui…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Native Promotions, Inc.
FDA (openFDA drug enforcement)
Reported Sep 8, 2021
DIAMONDBACK 360 GEN2 PERIPHERAL ORBITAL ATHERECTOMY SYSTEM, 1.5MM SOLID, 145 CM, REF DBP-150SOLID145
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 8, 2021
Flourless Chocolate Torte, 14 oz., in recyclable plastic circular container with black base and clear lid, Gem City…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gem City Fine Foods, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 8, 2021
Donepezil HCL Tablets, USP, 5 mg, 90-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd. India, Marketed by:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Jubilant Cadista Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Sep 1, 2021
Bleomycin for Injection, USP, packaged in 15 units per single dose vial, Rx only, Manufactured by Thymoorgan Pharmazie…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hikma Pharmaceuticals USA Inc.
FDA (openFDA drug enforcement)
Reported Sep 1, 2021
PDI Povidone-Iodine Prep Pad MEDIUM, 1 Prep Pad [2.0x2.5 in (5.1x6.4 cm)], Professional Disposables International Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Professional Disposables International, Inc.
6 more products in this recall
FDA (openFDA drug enforcement)
Reported Aug 25, 2021
ECHELON FLEX Powered Plus Stapler-intended for transection, resection, and/or creation of anastomoses. The instruments…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Aug 18, 2021
Grasper/Retriever, Alligator Jaw 2.4 mm x 5 mm x 230 cm Catalog Number: 7208 Intended use: single use accessory devices…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shent USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 28, 2021
Disposable Replacement Backflush Brush Needles (23 gauge/0.6mm)-for use in vitreoretinal surgery Product Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dutch Ophthalmic USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 21, 2021
B-Force, Homeopathic, 1 Fl Oz (30 mL) bottle, Distributed by: BioActive Nutritional, Inc., Melbourne, FL 32935, NDC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Grato Holdings, Inc.
FDA (openFDA drug enforcement)
Reported Jul 14, 2021
Buprenorphine and Naloxone Sublingual Film 2mg/0.5mg, 30 pouches each containing 1 sublingual film, Distributed by:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alvogen, Inc.
FDA (openFDA drug enforcement)
Reported Jul 7, 2021
QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)), 16.9 FL OZ (500 ML) bottles, Manufactured by: Guangzhou Minghui…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hoyu(us) Logistics Inc.
FDA (openFDA drug enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.