safco SensiCaine-Ultra (20% Benzocaine), Topical Anesthetic Gel, Strawberry Flavor, 1 oz. (29.6mL), Distributed by: Safco…
Reason Defective container:may contain bottles with incomplete seals
23 FDA recalls mention Strawberry. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Strawberry.
Reason Defective container:may contain bottles with incomplete seals
Reason Defective container:may contain bottles with incomplete seals
Reason Defective container:may contain bottles with incomplete seals
Reason Defective container:may contain bottles with incomplete seals
Reason Defective container:may contain bottles with incomplete seals
Reason Defective container:may contain bottles with incomplete seals
Reason This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the…
Reason CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Reason Labeling: Not Elsewhere Classified: Back label states Each contains: cephalexin monohydrate, USP equivalent to 2.5g' instead of Each Bottle…
Reason Microbial contamination of Non-Sterile Product; presence of yeast identified as Candida parapsilosis
Reason Labeling: Label Mix-Up: Some hello wild strawberry fluoride toothpaste, packaged in cartons labeled as hello wild strawberry fluoride toothpaste were…
Reason CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Reason CGMP Deviations: product held outside appropriate storage temperature conditions.
Reason Lack of Processing Controls: Insanitary conditions observed during recent FDA Inspection
Reason cGMP deviations: Temperature abuse
Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Reason Marketed without an Approved NDA/ANDA: Product marketed with drug claims.
Reason Chemical contamination: product contains elevated levels of undeclared lead.
Reason Chemical contamination: product contains elevated levels of undeclared lead.
Reason CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC products.
Reason Labeling: Label Error on Declared Strength; the label states that the product contains 62% ethyl alcohol, but the ethyl alcohol content is 20%.
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