FDA Closes Botticelli Foods Pistachio Nut Butter Recall
The FDA has closed its enforcement action on the bettergoods pistachio nut butter recall, meaning the agency considers the recall carried out.
Recalls & Safety Alerts in New York
Every recalls & safety alerts report published for New York, newest first.
FDA Closes Recall of Mehadrin Chocolate Leben Cups Over Pasteurization Concern
The FDA has closed the Class II recall of Mehadrin Chocolate Leben cups, initiated after possible improper pasteurization.
FDA Closes Recall of American Regent Cyanocobalamin Injection Over Particulate Contamination
The FDA has closed the Class II recall of certain cyanocobalamin injection vials, confirming the action is complete.
American Regent Recalls Acetylcysteine Solution Over Particulate Contamination
FDA classifies recall of 169,200 vials as Class II due to hair, glass, and paraformaldehyde particles.
FDA Class I Recall: Papaverine HCl Injection Vials Contaminated with Glass and Paraformaldehyde
American Regent, Inc. recalls 86,100 vials of Papaverine HCl Injection due to particulate matter contamination.
American Regent Recalls Acetylcysteine Solution Over Particulate Contamination
FDA Class II recall of 316,450 vials due to hair, glass, and paraformaldehyde particles.
American Regent Recalls Atropine Sulfate Injection Due to Particulate Contamination
FDA Class II recall of 89,775 vials of atropine sulfate injection after contamination with hair, glass, and paraformaldehyde was identified.
American Regent Recalls Nitroglycerin Injection Over Particulate Contamination
FDA classifies recall of 98,200 vials as Class II due to hair, glass, and paraformaldehyde particles.
Intersurgical Inc Recalls One-Piece Guedel Airways Due to Potential Occlusion
FDA Class II recall of 1,575 airway devices distributed nationwide.
Intersurgical Inc Recalls One-Piece Guedel Airways Over Potential Occlusion
FDA classifies recall of 21,269 airway devices as Class II due to possible blockage.
FDA Closes Recall of Regeneron's Libtayo Injection Over Sterility Assurance
The FDA has closed the Class II recall of Libtayo (cemiplimab-rwlc) Injection, lot 8494000002, initiated by Regeneron Pharmaceuticals over lack of assurance of sterility.
American Regent Recalls Multrys Injection Due to Particulate Contamination
FDA Class II recall of 185,775 vials of Multrys Trace Elements Injection 4, USP, due to particulate matter identified as hair, glass and/or paraformaldehyde.
FDA Recalls Clear Eyes Maximum Itchy Eye Relief Over Sterility Concerns
Prestige Brands Holdings recalls 39,060 bottles of Clear Eyes Maximum Itchy Eye Relief due to potential contamination.
FDA Class I Recall: Kian Pee Wan Capsules Contain Undeclared Drug Ingredients
Buy-Herbal recalls 71 bottles of Kian Pee Wan Capsules sold on eBay because they contain undeclared dexamethasone and cyproheptadine.
FDA Closes Recall Action for Unlabeled Soft Ricotta Cheese in New York
The FDA considers the recall carried out for Nelson & Isa Lacteos LLC soft ricotta cheese.
FDA Reports Class II Recall of Siemens Atellica CH Urine Albumin Diagnostic
Siemens Healthcare Diagnostics, Inc. has initiated an ongoing recall of 7018 units of Atellica CH Urine Albumin.
FDA Lists Class II Recall of Brooklyn Roasting Cold Brew Concentrate Over Botulinum Risk
An enforcement report dated July 29, 2026 records an ongoing recall of 1,219 bag-in-box units distributed in New York and New Jersey.
FDA Records Ongoing Class II Recall of Nutricia Nourish Berry Medley Formula Over Subpotent Vitamin A
An FDA enforcement report dated July 22, 2026 lists a recall initiated May 26, 2026 covering pouches shipped to 48 US jurisdictions, Canada and Australia.
FDA Lists Class I Nationwide Recall of Two TNVitamins Moringa Products Over Salmonella
An FDA enforcement report records 8,492 units of moringa capsules and powder distributed by Total Nutrition Inc as contaminated with Salmonella, in an action the agency lists as ongoing.
FDA Lists Class II Recall of Liquid Hope Berry Medley Feeding Formula for Subpotent Vitamin A
The agency's enforcement record for recall H-1152-2026 says a testing laboratory used the wrong method, overstating the vitamin A concentration in the Nutricia North America product.