FoodJun 19, 2024
Grande Bravo 550 Functional Whey Protein SKU 32105 recall — FDA F-1365-2024
Possible Salmonella contamination.
Class IFDA: TerminatedGRANDE CHEESE COMPANY
June 2024 recalls — page 4
These records include useful source details for the selected month.
FoodJun 19, 2024
Kerry Salt & Vinegar 620592 Net Weight: 50lb recall — FDA F-1356-2024
Potential Salmonella Contamination.
Class IFDA: TerminatedKerry, Inc.
FoodJun 19, 2024
Kerry Sun Nat HV CHDR #3 SEAS, Net Weight: 50.00 lb recall — FDA F-1355-2024
Potential Salmonella Contamination.
Class IFDA: TerminatedKerry, Inc.
FoodJun 19, 2024
Kerry BrS8 RODIZIO Seas No MSG 9.6#, SAP Code: 20644205 recall — FDA F-1354-2024
Potential Salmonella Contamination.
Class IFDA: TerminatedKerry, Inc.
FoodJun 19, 2024
Grande Bravo 300 Functional Whey Protein SKU 32102 recall — FDA F-1363-2024
Possible Salmonella contamination.
Class IFDA: TerminatedGRANDE CHEESE COMPANY
DrugJun 19, 2024
Imprimis NJOF Klarity-C (cyclosporine) Preservative-Free Sterile Ophthalmic Emulsion 0.1% recall — FDA D-0547-2024
Lack of Assurance of Sterility
Class IIFDA: OngoingImprimis NJOF, LLC
DrugJun 19, 2024
RemedyRepack Phenazopyridine HCl, 100mg tablets, 6 count bottles recall — FDA D-0549-2024
Product Mix Up. A bottle labeled as Phenazopyridine HCl tablets USP 100 mg contained Phenobarbital tablets 16.2 mg.
Class IIFDA: TerminatedRemedyRepack Inc.
DrugJun 19, 2024
Docetaxel Injection, USP, 80 mg per 8 mL (10 mg per mL), 1 x 8 mL Multi-Dose Vial recall — FDA D-0553-2024
Presence of Particulate Matter: Presence of particulate matter from the stopper in the drug product.
Class IFDA: OngoingSagent Pharmaceuticals
DrugJun 19, 2024
ZILRETTA Drug Vial Label: Zilretta recall — FDA D-0546-2024
Failed Stability Specifications - at 12 months 2-8 degrees C followed by 6 weeks at 25 degrees C.
Class IIFDA: OngoingPACIRA PHARMACEUTICALS Inc.
DrugJun 19, 2024
Docetaxel Injection, USP, 160 mg per 16 mL (10 mg per mL), 1 x 16 mL Multi-Dose Vial recall — FDA D-0554-2024
Presence of Particulate Matter: Presence of particulate matter from the stopper in the drug product.
Class IFDA: OngoingSagent Pharmaceuticals
DrugJun 19, 2024
Phenazopyridine HCl Tablets USP, 100 mg, 100-count bottles recall — FDA D-0545-2024
Product Mix Up. A bottle of Phenazopyridine HCl tablets USP 100 mg contained Phenobarbital tablets 16.2 mg.
Class IIFDA: CompletedWinder Laboratories, LLC
VehicleJun 18, 2024
Highlander tires recall — NHTSA campaign 24V452000
Southeast Toyota Distributors, LLC (SET) is recalling certain 2021-2024 Highlander vehicles. The 20-inch accessory tires with an insufficient load rating for the vehicle's Gross Axle Weight…
tiresSoutheast Toyota Distributors, LLC
VehicleJun 14, 2024
Escape two-wheel drive adaptive cruise control recall — NHTSA campaign 24V440000
Ford Motor Company (Ford) is recalling certain 2023-2024 Escape two-wheel drive vehicles equipped with adaptive cruise control. The cruise control radar module was misaligned during…
adaptive cruise controlFord Motor Company
VehicleJun 14, 2024
F-150 body control module software recall — NHTSA campaign 24V443000
Ford Motor Company (Ford) is recalling certain 2021 F-150 vehicles equipped with the Onboard Scales feature. An over-the-air software update to the body control module (BCM) may have…
body control module softwareFord Motor Company
VehicleJun 13, 2024
Jeep Grand Cherokee critical fasteners recall — NHTSA campaign 24V434000
Chrysler (FCA US, LLC) is recalling certain 2023 Jeep Grand Cherokee vehicles. A bolt for the second-row seat belt buckle may not be tightened properly. As such, these vehicles fail to…
critical fastenersChrysler (FCA US, LLC)
VehicleJun 13, 2024
Chrysler camera recall — NHTSA campaign 24V436000
Chrysler (FCA US, LLC) is recalling certain 2021-2022 Dodge Durango, 2021-2023 Chrysler Pacifica, Jeep Grand Cherokee L, 2022 Ram 1500, 2500, 3500, Chrysler Voyager, 2022-2023 Jeep Compass,…
cameraChrysler (FCA US, LLC)
VehicleJun 13, 2024
Chrysler camera recall — NHTSA campaign 24V437000
Chrysler (FCA US, LLC) is recalling one 2022 Ram 1500 Classic vehicle. The wiring harness may short circuit and prevent the rearview image from displaying. As such, this vehicle fails to…
cameraChrysler (FCA US, LLC)
Medical DeviceJun 12, 2024
MEDLINE STERILE IRIS SCISSORS CVD/STD REF DYNJ04049 (case) and DYNJ04049H (individual unit) recall — FDA Z-2024-2024
There is the potential of the tip protector to fall off 4.5" sterile, curved, Iris Scissors
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceJun 12, 2024
Getinge Usa Sales Vaporizer Sevoflurane Maquet Filling, Product code/REF number (6682282) recall — FDA Z-1877-2024
Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health care providers through inhalation and/or skin exposure. Potential…
Class IFDA: OngoingGetinge Usa Sales Inc.
Medical DeviceJun 12, 2024
Atrium Medical ADVANTA VXT, 5X40, 1GDS, NH, STR-SW recall — FDA Z-1951-2024
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Class IIFDA: OngoingAtrium Medical Corporation
Medical DeviceJun 12, 2024
Atrium Medical ADVANTA VXT, 7X50, 1GDS, FH, STR-TW recall — FDA Z-1984-2024
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Class IIFDA: OngoingAtrium Medical Corporation
Medical DeviceJun 12, 2024
Becton Dickinson & Co BD SARS-CoV-2 Reagents for BD MAX" Systems recall — FDA Z-2023-2024
Assays may produce false negative results due to decreased activity of the enzyme utilized in manufacturing.
Class IIFDA: OngoingBecton Dickinson & Co.
Medical DeviceJun 12, 2024
Atrium Medical ADVANTA VXT, 8X50, 1GDS, FH, STR-TW recall — FDA Z-1985-2024
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Class IIFDA: OngoingAtrium Medical Corporation
Medical DeviceJun 12, 2024
Olympus Corporation of the Americas OES 4000 Hysteroscope recall — FDA Z-2029-2024
The required leakage test was not performed following of a re-work for a non-conformity. This could potentially result in liquid ingress into the eyepiece and cause a foggy image.
Class IIFDA: OngoingOlympus Corporation of the Americas
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.