FoodSep 22, 2021
Full Tilt Ice Cream Salted Caramel, brand Full Tilt Ice Cream, packaged in 16oz recall — FDA F-0962-2021
The ice cream mix did not meet pasteurization specifications.
Class IIFDA: TerminatedFull Tilt Ice Cream, LLC
September 2021 recalls — page 6
These records include useful source details for the selected month.
FoodSep 22, 2021
Full Tilt Ice Cream Mexican Chocolate, Full Tilt Ice Cream brand, packaged in 16oz recall — FDA F-0963-2021
The ice cream mix did not meet pasteurization specifications.
Class IIFDA: TerminatedFull Tilt Ice Cream, LLC
FoodSep 22, 2021
Naturo Aid Pharmaceutical Vita Aid Keto-Elemental Nutrition recall — FDA F-0976-2021
Undeclared Milk. Products may be contaminated with milk residue.
Class IIFDA: TerminatedNaturo Aid Pharmaceutical Inc.
FoodSep 22, 2021
Loki Fish Company - Office packaged in a 4 oz recall — FDA F-1005-2021
Potential to be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedLoki Fish Company - Office
FoodSep 22, 2021
Jimbo's BLOODY MARY MIX recall — FDA F-0982-2021
Product contains soy, sulfites, and wheat that are not declared in the ingredient statement.
Class IIFDA: TerminatedJimbo's Kitchen
FoodSep 22, 2021
Jimmy's Cookies Marketside Chocolate Candy Cookie Cake, 24 oz recall — FDA F-0961-2021
Undeclared allergen - Peanuts.
Class IFDA: TerminatedJimmy's Cookies, LLC
FoodSep 22, 2021
Full Tilt Ice Cream Vanilla Bean, Full Tilt Ice Cream, packaged in 16oz pre packed recall — FDA F-0966-2021
The ice cream mix did not meet pasteurization specifications.
Class IIFDA: TerminatedFull Tilt Ice Cream, LLC
FoodSep 22, 2021
Naturo Aid Pharmaceutical Vita Aid SynerClear recall — FDA F-0980-2021
Undeclared Milk. Products may be contaminated with milk residue.
Class IIFDA: TerminatedNaturo Aid Pharmaceutical Inc.
FoodSep 22, 2021
Organic By Nature Purim Health Products: EpiGenius Kids Creamy Chocolate recall — FDA F-0975-2021
Product recalled due to undeclared milk in MCT powder used in manufacturing. Milk is not declared on the label. Product item #'s 4600-P65, 4600
Class IFDA: TerminatedOrganic By Nature, Inc.
FoodSep 22, 2021
Full Tilt Ice Cream Backyard mint chip, Full Tilt Ice Cream brand, packaged in recall — FDA F-0964-2021
The ice cream mix did not meet pasteurization specifications.
Class IIFDA: TerminatedFull Tilt Ice Cream, LLC
FoodSep 22, 2021
Naturo Aid Pharmaceutical Vita Aid SynerClear recall — FDA F-0978-2021
Undeclared Milk. Products may be contaminated with milk residue.
Class IIFDA: TerminatedNaturo Aid Pharmaceutical Inc.
DrugSep 22, 2021
Grupo Asimex de Mexico SA de CV Florance Morris ANTISEPTIC Hand Sanitizer recall — FDA D-0796-2021
CGMP Deviations: All other lots are being recalled because they were manufactured under the same conditions as the product lots found to contain methanol.
Class IIFDA: TerminatedGrupo Asimex de Mexico SA de CV
DrugSep 22, 2021
Oxycodone Hydrochloride Tablets, USP, 10 mg, 100 count bottle recall — FDA D-0794-2021
Presence of Foreign Tablets/Capsules; A single foreign tablet Hydrochlorothiazide/Lisinopril 25/20 was found in one bottle
Class IIFDA: TerminatedRhodes Pharmaceuticals, L.P.
DrugSep 22, 2021
Akorn Betamethasone Dipropionate Lotion USP (Augmented), 0.05% recall — FDA D-0802-2021
Failed impurities/degradation specification: Out of Specification for an unknown impurity observed in topical product.
Class IIFDA: TerminatedAkorn, Inc.
DrugSep 22, 2021
ICU Medical AMINOSYN II 15% An Amino Acid Injection, Sulfite-Free, 2000 mL in flexible recall — FDA D-0805-2021
Presence of Particulate Matter: Particulate matter identified as fibers, hair, and proteinaceous material along with other particles, found in retain smples.
Class IFDA: TerminatedICU Medical Inc.
DrugSep 22, 2021
70% ISOPROPYL RUBBING ALCOHOL Kroger 70% Isopropyl Alcohol First Aid Antiseptic 32 FL OZ recall — FDA D-0799-2021
Labeling: Label Mix-Up.The recall has been initiated after receiving one complaint about incorrect labeling.The primary label on the front and back label on some of the bottles have 70%…
Class IIFDA: TerminatedVi-Jon, Inc.
DrugSep 22, 2021
Grupo Asimex de Mexico SA de CV Florance Morris ANTISEPTIC Hand Sanitizer recall — FDA D-0795-2021
Chemical Contamination: FDA analysis found the product contains methanol, additionally it is sub-potent for ethanol content.
Class IFDA: TerminatedGrupo Asimex de Mexico SA de CV
VehicleSep 22, 2021
Ford back over prevention software recall — NHTSA campaign 21V735000
Ford Motor Company (Ford) is recalling certain 2020-2021 Explorer, Lincoln Corsair, and Lincoln Aviator vehicles equipped with 360-degree cameras. The video output may fail, preventing the…
back over prevention softwareFord Motor Company
VehicleSep 21, 2021
Jeep Grand Cherokee L rearview mirrors/devices recall — NHTSA campaign 21V729000
Chrysler (FCA US, LLC) is recalling certain 2021 Jeep Grand Cherokee L vehicles. A radio software error may prevent the rearview image from displaying. As such, these vehicles fail to…
rearview mirrors/devicesChrysler (FCA US, LLC)
Medical DeviceSep 15, 2021
Philips recall — FDA Z-2427-2021
Infant/Child defibrillator pads contain incorrect labeling. This could lead to a delay in therapy, or delivery of lower energy than indicated for an adult patient
Class IIFDA: TerminatedPhilips North America LLC
Medical DeviceSep 15, 2021
Angiodynamics Solero Generator PG, Item No recall — FDA Z-2439-2021
Specific serial numbers of the Solero MTA Generator require servicing to upgrade the software to help reduce the incidence of Error 0001, which can occur during system start-up.
Class IIFDA: TerminatedAngiodynamics, Inc.
Medical DeviceSep 15, 2021
Angiodynamics Solero Generator Refurbished PG, Item No recall — FDA Z-2438-2021
Specific serial numbers of the Solero MTA Generator require servicing to upgrade the software to help reduce the incidence of Error 0001, which can occur during system start-up.
Class IIFDA: TerminatedAngiodynamics, Inc.
Medical DeviceSep 15, 2021
Philips SmartPath to dStream for 1.5T-a Magnetic Resonance Medical Electrical Systems recall — FDA Z-2415-2021
When using manual mode, the tabletop may not completely move in or out and result in potential delay in patient evacuation from the bore, which could result in a delay of treatment
Class IIFDA: CompletedPhilips North America LLC
Medical DeviceSep 15, 2021
Philips Ingenia 1.5T S-a Magnetic Resonance Medical Electrical Systems indicated for use as recall — FDA Z-2413-2021
When using manual mode, the tabletop may not completely move in or out and result in potential delay in patient evacuation from the bore, which could result in a delay of treatment
Class IIFDA: CompletedPhilips North America LLC
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.