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All product recalls associated with Arctic Zero, Inc..
Total Recalls
1000
Past Year
304
Class I (Serious)
34
Most Recent
Nov 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due to undeclared milk.
Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due to undeclared milk.
Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due to undeclared milk.
Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due to undeclared milk.
Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due to undeclared milk.
Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due to undeclared milk.
Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due to undeclared milk.
Impurities/Degradation Products: Out of specification results for Related Compound during routine stability testing.
Chemical Contamination: This product is being recalled because trace amounts of a plasticizer (Di-Octyl Phthalate) may be present in the product.
Labeling: Label Mix-up: Pitocin storage conditions should be labeled, "Store between 20¿ to 25¿C (68¿ to 77¿F)". Pitocin lot 225867 and part of Pitocin lot 231423 were labeled, "Store between 20¿ to 25¿C (28¿ to 77¿F)".
GMP deviation; Sr-82 levels exceeded alert limit specification
Impurities/Degradation Products: A confirmed out of specification result for Leukine sargramostin lot B18827 occurred at the three month time point.
Presence of Foreign Substance: Recall is being initiated due to the presence of a foreign particle identified from a customer complaint.
Tablet Thickness: Potential for some tablets not conforming to weight specifications (under and over weight)
Cross Contamination w/Other Products: This active pharmaceutical ingredient is being recalled due to cross contamination with another product.
Subpotent; fluocinolone acetonide
Subpotent; fluocinolone acetonide
Adulterated Presence of Foreign Tablets: Customer complaint that some Endocet 10 mg/325 mg tablets were found mixed in a bottle with Endocet 10 mg/650 mg tablets.
Impurities/Degradation: This recall is being carried out due to the potential for some lots not meeting impurity specifications.
Presence of Particulate Matter