FoodOct 23, 2024
Lemonland Food Item FLD1010A, Seasoned Peanut, distributed in plastic recall — FDA F-0047-2025
Soy Sauce is declared but Wheat is not declared.
Class IIIFDA: TerminatedLemonland Food Corp
Monthly breakdown
2024 recalls by month
Select a month to review the recall records reported during that period.
December 2024325 records · 4 categoriesNovember 2024355 records · 4 categoriesOctober 2024409 records · 4 categoriesSeptember 2024547 records · 4 categoriesAugust 2024327 records · 4 categoriesJuly 2024318 records · 4 categoriesJune 2024286 records · 4 categoriesMay 2024422 records · 4 categoriesApril 2024323 records · 4 categoriesMarch 2024332 records · 4 categoriesFebruary 2024425 records · 4 categoriesJanuary 2024298 records · 4 categories
2024 recalls — page 37
Records are ordered by the best available source date.
FoodOct 23, 2024
Pacific Coast Fresh CO King Harvest Spinach Hummus, perishable and refrigerated recall — FDA F-0031-2025
Recall initiated due to potential plastic fragments.
Class IIFDA: TerminatedPacific Coast Fresh CO
FoodOct 23, 2024
Lemonland Food Item FLD1080A, Seasoned Radish, distributed in plastic recall — FDA F-0043-2025
Undeclared Crustacean (shrimp).
Class IFDA: TerminatedLemonland Food Corp
FoodOct 23, 2024
Today's Frozen Desserts Premium Grapenut Special, packaged in paper and plastic recall — FDA F-0030-2025
Undeclared Yellow 5 & Yellow 6
Class IIFDA: TerminatedToday's Frozen Desserts, Inc.
FoodOct 23, 2024
Lemonland Food Item FLD2011, Salted and Seasoned Small Octopus, distributed recall — FDA F-0046-2025
Undeclared Fish (Anchovy).
Class IFDA: TerminatedLemonland Food Corp
FoodOct 23, 2024
Hydration Labs Inc. dba Bevi Flavor#115 Electrolytes, Net Contents 3.78L, #740-0115, GTIN recall — FDA F-0034-2025
Product is labeled as electrolytes but is actually caffeine
Class IIFDA: TerminatedHydration Labs Inc. dba Bevi
FoodOct 23, 2024
Lemonland Food Item FLD1971, Stir Fried Dried Shrimp, distributed in plastic recall — FDA F-0050-2025
Soy Sauce is declared but Wheat is not declared.
Class IIIFDA: TerminatedLemonland Food Corp
FoodOct 23, 2024
Lemonland Food Item FLD1040A, Wild Leeks, distributed in plastic clamshell recall — FDA F-0049-2025
Soy Sauce is declare but Wheat and Fish (Anchovy) are not declared.
Class IIFDA: TerminatedLemonland Food Corp
DrugOct 23, 2024
Cisplatin Injection, 100mg/100mL (1mg/mL), For Intravenous Use, 100 mL Multiple Dose Vial recall — FDA D-0010-2025
Failed Impurities/Degradation Specifications.
Class IIFDA: TerminatedACCORD HEALTHCARE, INC.
DrugOct 23, 2024
Atovaquone Oral Suspension, USP 750 mg/5 mL, 210 mL bottle recall — FDA D-0012-2025
Microbial Contamination of a Non-sterile Product: The product was found to be contaminated with Cohnella bacteria.
Class IFDA: TerminatedBionpharma Inc.
DrugOct 23, 2024
First Aid Antiseptic Ointment, Povidone Iodine USP 10%, Inactive Ingredients: mineral oil recall — FDA D-0013-2025
Incorrect/Undeclared Excipients: The inactive ingredients labeled on the product boxes and tubes are listed as "mineral oil , petrolatum ". The inactive ingredients in the actual product…
Class IIFDA: OngoingZhejiang Jingwei Pharmaceutical Co., Ltd.
VehicleOct 18, 2024
Maverick vehicle tether anchor recall — NHTSA campaign 24V778000
Ford Motor Company (Ford) is recalling certain 2024 Maverick vehicles. The second-row child seat tether anchors may not properly secure a child seat, due to incomplete thread engagement. As…
vehicle tether anchorFord Motor Company
VehicleOct 17, 2024
BMW cushion recall — NHTSA campaign 24V772000
BMW of North America, LLC (BMW) is recalling certain 2025 X3 xDrive30i and X3 M50i vehicles. The front passenger air bag fabric may have been damaged during transport between suppliers.
cushionBMW of North America, LLC
Medical DeviceOct 16, 2024
Becton Dickinson & Co BD Synapsys Informatics Solution with software versions: 4.20, 4.30 recall — FDA Z-0026-2025
Synapsys software versions 4.20, 4.30, 5.10, 5.20, or 5.30 and utilizing the in-line breakpoint feature, an error is occurring where BD Synapsys will incorrectly display breakpoints for…
Class IIFDA: OngoingBecton Dickinson & Co.
Medical DeviceOct 16, 2024
Beckman Coulter Dxl 9000 Access Immunoassay Analyzer, REF #C11137 recall — FDA Z-0025-2025
When the DxI 9000 Access Immunoassay Analyzer with system software version 1.16.2 and prior is configured to automatically request a calibration order, the instrument can process the order…
Class IIFDA: OngoingBeckman Coulter, Inc.
Medical DeviceOct 16, 2024
Stryker Neurovascular The Trevo Trak 21 Microcatheter is a single-lumen, braided shaft recall — FDA Z-0021-2025
Stryker Neurovascular has observed that devices with Out of United States (OUS) approved Instructions for Use (IFU) and Packaging Labels (pouch and carton), different configurations, have…
Class IIFDA: OngoingStryker Neurovascular
Medical DeviceOct 16, 2024
Luminex Molecular Diagnostics NxTAG Respiratory Pathogen Panel, REF: I051C0447 recall — FDA Z-0042-2025
Respiratory pathogen panel may report an elevated rate (7.6% predicted probability of occurrence) of non-specific hMPV target (human Metapneumovirus) results, risk identified predominantly…
Class IIFDA: OngoingLuminex Molecular Diagnostics Inc.
Medical DeviceOct 16, 2024
Inspire Model 4063 Stimulation Lead, component of the Inspire Upper Airway Stimulation (UAS) recall — FDA Z-0041-2025
Labeling error with a mismatch between the shelf box serial number label and the serial number of the lead provided in the box.
Class IIFDA: OngoingInspire Medical Systems Inc.
Medical DeviceOct 16, 2024
MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001 recall — FDA Z-0032-2025
It has been determined that certain Blood Pressure Monitors containing a faulty microchip have failed to power on or have shown display screen issues after the initial few uses, as well as…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 16, 2024
AURIS HEALTH Monarch Platform (Urology), REF: MON-000007, MON-000007-RFB recall — FDA Z-0052-2025
Endoscopy/bronchoscopy/urology devices may have a strain relief defect with some cart and tower power cords that may cause an electrical short, which may lead to system shutdown, which can…
Class IIFDA: OngoingAURIS HEALTH Inc.
Medical DeviceOct 16, 2024
MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001U recall — FDA Z-0033-2025
It has been determined that certain Blood Pressure Monitors containing a faulty microchip have failed to power on or have shown display screen issues after the initial few uses, as well as…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 16, 2024
Windstone Medical Packaging Aligned Medical Tonsil ENT Pack REF AMS9977 that contains the recall — FDA Z-0028-2025
Due to convenience kits containing a kit component that is under a recall action for improper use.
Class IIFDA: OngoingWindstone Medical Packaging, Inc.
Medical DeviceOct 16, 2024
Howmedica Osteonics Triathlon Universal TS Baseplate Size 2 - A single use sterile recall — FDA Z-0023-2025
Anterior locking tabs on the Triathlon Universal Baseplate are out of specification which may prevent engagement of either of the two locking tabs with the locking wire of the tibial insert.
Class IIFDA: OngoingHowmedica Osteonics Corp.
Medical DeviceOct 16, 2024
Windstone Medical Packaging Aligned Medical Tonsil Pack REF AMS14809 that contains the recall — FDA Z-0031-2025
Due to convenience kits containing a kit component that is under a recall action for improper use.
Class IIFDA: OngoingWindstone Medical Packaging, Inc.
About the 2024 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.