FoodNov 22, 2023
Paradise Flavors Cookies And Cream, distributed by Paradise Flavors LLC, 4 OZ recall — FDA F-0449-2024
Undeclared allergens: Milk, soy, and wheat.
Class IFDA: TerminatedParadise Flavors LLC
Monthly breakdown
2023 recalls by month
Select a month to review the recall records reported during that period.
December 2023295 records · 4 categoriesNovember 2023387 records · 4 categoriesOctober 2023214 records · 4 categoriesSeptember 2023253 records · 4 categoriesAugust 2023478 records · 4 categoriesJuly 2023263 records · 4 categoriesJune 2023339 records · 4 categoriesMay 2023410 records · 4 categoriesApril 2023189 records · 4 categoriesMarch 2023788 records · 4 categoriesFebruary 2023253 records · 4 categoriesJanuary 2023205 records · 4 categories
2023 recalls — page 20
Records are ordered by the best available source date.
FoodNov 22, 2023
Tay's Sales and Distribution Full Spectrum Cold Pressed Hemp Oil Gummies, Pomegranate, 1.41 recall — FDA F-0417-2024
Sub-ingredients not declared for sunflower butter.
Class IIFDA: CompletedTay's Sales and Distribution
DrugNov 22, 2023
Omega & Delta Co DOP Instant Hand Sanitizer (Ethyl Alcohol 65%) with Moisturizers, Original recall — FDA D-0103-2024
Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer product, it was identified that several lots distributed did not comply with the finished good…
Class IIFDA: OngoingOmega & Delta Co., Inc.
DrugNov 22, 2023
Omega & Delta Co DOP Instant Hand Sanitizer (Ethyl Alcohol 65%) with Moisturizers, 8FL OZ recall — FDA D-0104-2024
Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer product, it was identified that several lots distributed did not comply with the finished good…
Class IIFDA: OngoingOmega & Delta Co., Inc.
DrugNov 22, 2023
Omega & Delta Co Equate Hand Sanitizer (Ethyl Alcohol 62%), 7.5 FL.OZ. (221 mL) UPC 6 81131 recall — FDA D-0105-2024
Sub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer product, it was identified that several lots distributed did not comply with the finished good…
Class IIFDA: OngoingOmega & Delta Co., Inc.
VehicleNov 22, 2023
Rogue caliper recall — NHTSA campaign 23V791000
Nissan North America, Inc. (Nissan) is recalling certain 2021 Rogue vehicles. The left and/or right rear brake caliper assemblies may be missing an internal bushing, allowing the O-ring…
caliperNissan North America, Inc.
VehicleNov 22, 2023
Jeep Wrangler Plug-In Hybrid Electric (PHEV) traction battery recall — NHTSA campaign 23V787000
Chrysler (FCA US, LLC) is recalling certain 2021-2023 Jeep Wrangler Plug-In Hybrid Electric (PHEV) vehicles. The high voltage battery may fail internally and lead to a vehicle fire while…
traction batteryChrysler (FCA US, LLC)
VehicleNov 21, 2023
S60 frontal air bag recall — NHTSA campaign 23V780000
Volvo Car USA, LLC. (Volvo Car) is recalling certain 2019-2024 S60 vehicles. The passenger air bag may not be secured properly, which can cause the air bag to deploy improperly.
frontal air bagVolvo Car USA, LLC
VehicleNov 21, 2023
Honda front recall — NHTSA campaign 23V782000
Honda (American Honda Motor Co.) is recalling certain 2023-2024 Accord and HR-V vehicles. The front seat belt pretensioners may be missing the rivet that secures the quick connector and…
frontHonda (American Honda Motor Co.)
Medical DeviceNov 15, 2023
CareFusion 303 BD Alaris PCU REF 8015 recall — FDA Z-0184-2024
Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump: compatible syringes labeling contains syringes that have not been validated.
Class IFDA: OngoingCareFusion 303, Inc.
Medical DeviceNov 15, 2023
B. Braun Medical BULK LARGEBORE MALE LL FITTING, Article No recall — FDA Z-0136-2024
Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and healthcare…
Class IIFDA: OngoingB. Braun Medical, Inc.
Medical DeviceNov 15, 2023
Family Dollar Stores, LLC VERIQUICK PREGNANCY TEST 1CT, SKU 901260 recall — FDA Z-0264-2024
Products were stored outside of labeled temperature requirements.
Class IIFDA: OngoingFamily Dollar Stores, LLC.
Medical DeviceNov 15, 2023
Stryker Disposable Spetzler-Malis Bipolar forceps, 20CM SLM DISP BAYONET 0.5MM, Catalog recall — FDA Z-0252-2024
An error was identified on the expiration date of the product label. The shelf life for the products impacted is 36 months (3 years) however the product label represents a 54 month (4.5…
Class IIFDA: OngoingStryker Corporation
Medical DeviceNov 15, 2023
Encore Medical RSP Humeral Small Socket Insert Size 32 mm Semi-Constrained +4, e-plus, REF recall — FDA Z-0281-2024
Two different humeral socket Insert devices were swapped during packaging, which could result in surgeons not having the correct device for surgery, which could cause a delay in surgery.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceNov 15, 2023
BREG REF 100519-000 WALKER FOLDING WALKER WITH WHEELS Utilized as a walking aid recall — FDA Z-0231-2024
Due to walkers not meeting product specifications. Walkers were manufactured with misaligned wheels.
Class IIFDA: OngoingBreg Inc.
Medical DeviceNov 15, 2023
Philips Integris-Allura IGTS Fixed Systems recall — FDA Z-0227-2024
Philips has become aware of an issue with the Philips Integris-Allura, Allura Xper and Azurion systems that have been delivered to Puerto Rico without a warning label and the Source-to-Skin…
Class IIFDA: OngoingPhilips North America
Medical DeviceNov 15, 2023
Medtronic Navigation StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The recall — FDA Z-0188-2024
Due to a software anomaly which potentially could result in the surgical planning data shifting to an unintended location.
Class IFDA: OngoingMedtronic Navigation, Inc.
Medical DeviceNov 15, 2023
B. Braun Medical SA3000 VENTED MICRO SPIKE ADAPTER, REF No. 418121, for intravenous use recall — FDA Z-0129-2024
Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and healthcare…
Class IIFDA: OngoingB. Braun Medical, Inc.
Medical DeviceNov 15, 2023
Stryker Disposable Spetzler-Malis Bipolar forceps, 23CM SLM DISP BAYONET 1.0MM, Catalog recall — FDA Z-0256-2024
An error was identified on the expiration date of the product label. The shelf life for the products impacted is 36 months (3 years) however the product label represents a 54 month (4.5…
Class IIFDA: OngoingStryker Corporation
Medical DeviceNov 15, 2023
Philips EPIQ Diagnostic Ultrasound System Models: EPIQ 7G(model # 795200), EPIQ 7C recall — FDA Z-0283-2024
Their is the potential that diagnostic ultrasound systems operating with software version 10.0 may present a delayed image instead of a real time image.
Class IIFDA: CompletedPhilips Ultrasound, Inc.
Medical DeviceNov 15, 2023
Change Healthcare Radiology Solutions, software versions 14.0, 14.1, and 14.2 Medical image recall — FDA Z-0237-2024
Change Healthcare has identified a software issue where Change Healthcare Radiology Solutions 14.0, 14.1, and 14.2 may not update records in external applications.
Class IIFDA: OngoingCHANGE HEALTHCARE CANADA COMPANY
Medical DeviceNov 15, 2023
Stryker Disposable Spetzler-Malis Bipolar forceps, 20CM SLM DISP BAYONET 1.5MM, Catalog recall — FDA Z-0254-2024
An error was identified on the expiration date of the product label. The shelf life for the products impacted is 36 months (3 years) however the product label represents a 54 month (4.5…
Class IIFDA: OngoingStryker Corporation
Medical DeviceNov 15, 2023
Stryker Disposable Spetzler-Malis Bipolar forceps, 18CM IM DISP BAYONET 0.5MM TIP, Catalog recall — FDA Z-0245-2024
An error was identified on the expiration date of the product label. The shelf life for the products impacted is 36 months (3 years) however the product label represents a 54 month (4.5…
Class IIFDA: OngoingStryker Corporation
Medical DeviceNov 15, 2023
B. Braun Medical FT1000S FLUID TRANSFER SET, REF No. 356048 recall — FDA Z-0128-2024
Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and healthcare…
Class IIFDA: OngoingB. Braun Medical, Inc.
About the 2023 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.