FDA Closes Recall of Zicam Nasal Swabs Over Microbiological Testing Deviations
The FDA has closed the Class II recall of certain Zicam Cold Remedy Medicated Nasal Swabs, citing CGMP deviations and out-of-limit microbiological test results.
Recalls & Safety Alerts in New Jersey
Every recalls & safety alerts report published for New Jersey, newest first.
Mallinckrodt recalls Acthar Gel vials over particulate matter
FDA classifies recall of 12,367 vials as Class II due to presence of glass and stopper pieces.
Heritage Pharmaceuticals recalls clindamycin oral solution over foreign particles
FDA classifies the nationwide recall as Class II, citing particles and white flakes found in reconstituted bottles.
FDA Class II Recall Issued for Diovan 160 mg Tablets Due to Failed Dissolution Specifications
Novartis Pharmaceuticals Corporation recalls one lot of Diovan (valsartan) 160 mg tablets after failing dissolution specifications, according to an FDA enforcement report.
FDA Records Show Ongoing Recall of Ophthalmic Solution Distributed by Micro Labs USA
An ongoing nationwide recall covers a lot of Dorzolamide HCl and Timolol Maleate Ophthalmic Solution due to container defects.
Glenmark Pharmaceuticals Recalls Azelaic Acid Gel Over Texture Complaints
An ongoing nationwide recall covers select lots of Azelaic Acid Gel, 15%, due to quality complaints of a grainy or sandy texture.
Aurobindo Pharma USA Recalls Dicyclomine Hydrochloride Capsules Over Empty Capsule Reports
An ongoing Class II recall covers 6,408 bottles of prescription dicyclomine hydrochloride capsules distributed nationwide.
FDA Reports Nationwide Recall of Mirabegron Extended-Release Tablets
Zydus Pharmaceuticals (USA) Inc. is recalling one lot of Mirabegron tablets due to an impurity finding in an ongoing Class II action.
FDA Posts Class II Recall of Canned Artichoke Hearts Over Glass Found in Product
An enforcement report lists 1,150 cases of quartered artichoke hearts distributed by Gellert Global Group to four northeastern states, with the recall status ongoing.
FDA Records Class I Recall of D'Dioses Limón Ice Pops Over Undeclared Milk, Nuts and Dyes
An FDA enforcement report dated July 22, 2026 lists 170 cases of the 4 oz lemon-lime paletas recalled across four Northeastern states, with the action ongoing.
FDA Records Class I Recall of D'Dioses Piña Colada Ice Pops Over Undeclared Milk and Nuts
An enforcement report lists 150 cases of the single-bar frozen pop recalled across four Northeastern states, with the action ongoing.
FDA Records Class II Recall of 6,192 Bottles of Blood-Pressure Combination Tablets
An FDA enforcement report lists an ongoing nationwide recall of one lot of amlodipine and olmesartan medoxomil tablets distributed by Ascend Laboratories over failed dissolution specifications.
FDA Records Class I Recall of D'Dioses Nanche Ice Pops Over Undeclared Milk, Nuts and Dyes
An enforcement report lists 120 cases of the 81.7 g bar recalled across four states, with the action still ongoing.
FDA Records Class I Recall of D'Dioses Mamey Ice Pops Over Undeclared Allergens
An FDA enforcement report lists 129 cases of a single-bar ice pop distributed in four Northeastern states as possibly containing undeclared milk, pecans, pistachios and two color additives.
FDA Lists Class I Recall of D'Dioses Arroz con Leche Ice Pops Over Undeclared Milk and Nuts
The agency's enforcement record cites 216 cases distributed in four Northeastern states, with the recall listed as ongoing.
FDA Lists Class I Recall of D'Dioses Fresa Leche Ice Pops Over Undeclared Allergens
The agency's enforcement report for recall H-1159-2026 cites possible undeclared milk, pecans, pistachios, yellow #5 and red #40 in 149 cases distributed across four states.
FDA Classifies Frozen Kimbap Recall as Class I Over Undeclared Fish Allergen
The agency's enforcement record lists 29,850 units of Fusia Asian Inspirations kimbap recalled by Gellert Global Group and distributed to six states.
FDA Records Class I Recall of D'Dioses Pistachio Ice Pops Over Undeclared Allergens
An FDA enforcement report dated July 22, 2026 lists 121 cases of a single-bar pistachio paleta as recalled in four Northeastern states because the label may not name milk, pecans, pistachios and two color additives.
FDA Lists Class I Recall of D'Dioses Nuez Ice Pops Over Undeclared Allergens
The agency's enforcement record cites possible undeclared milk, pecans, pistachios, yellow #5 and red #40 in 185 cases distributed across four states.
FDA Lists Class I Recall of D'Dioses Tamarindo Ice Pops Over Undeclared Allergens
The agency's enforcement record cites possible undeclared milk, pecans, pistachios and color additives in 129 cases distributed across four Northeastern states.
FDA Records Class I Recall of D'Dioses Cookies and Cream Ice Pops Over Undeclared Allergens
An FDA enforcement report lists 140 cases of the single-bar frozen dessert, distributed in four northeastern states, as possibly containing undeclared milk, pecans, pistachios and two colour additives.
FDA Lists Class I Recall of D'Dioses Mango Ice Pops Over Undeclared Milk, Nuts and Dyes
The agency's enforcement report for recall H-1171-2026 covers 167 cases distributed in four Northeastern states and lists the action as ongoing.