FoodDec 4, 2024
Treehouse Foods PICS BY PRICE CHOPPER 6/29.6oz GRDL WFL HSTYLE RF - PRCHP UPC recall — FDA F-0199-2025
potential to be contaminated with Listeria monocytogenes
Class IIFDA: TerminatedTreehouse Foods
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 14
Records are ordered by the best available source date.
FoodDec 4, 2024
Treehouse Foods DUNCAN HINES 1/3.12kg GRDL WFL BLGN ORIG 4IN - DUNHN UPC recall — FDA F-0179-2025
potential to be contaminated with Listeria monocytogenes
Class IIFDA: TerminatedTreehouse Foods
FoodDec 4, 2024
Treehouse Foods WEGMANS 12/7.4oz GRDL WFL MGRN ORG - WEGMN UPC 077890481431 recall — FDA F-0202-2025
potential to be contaminated with Listeria monocytogenes
Class IIFDA: TerminatedTreehouse Foods
FoodDec 4, 2024
Treehouse Foods KRUSTEAZ 1/2.5lb GRDL WFL BLGN 7-KRSTZ UPC 068615115168 recall — FDA F-0200-2025
potential to be contaminated with Listeria monocytogenes
Class IIFDA: TerminatedTreehouse Foods
FoodDec 4, 2024
Treehouse Foods WESTERN FAMILY 12/280g GRDL WFL CIN - WSTCN UPC 062639310134 recall — FDA F-0191-2025
potential to be contaminated with Listeria monocytogenes
Class IIFDA: TerminatedTreehouse Foods
FoodDec 4, 2024
Treehouse Foods GIANT EAGLE 12/11.3oz GRDL WFL BCKWHE BLBRY GF-GT/EG UPC recall — FDA F-0165-2025
potential to be contaminated with Listeria monocytogenes
Class IIFDA: TerminatedTreehouse Foods
FoodDec 4, 2024
Treehouse Foods H-E-B HIGHER HARVEST 12/10.72oz GRDL WFL BLBRY PRTN-HEBHH UPC recall — FDA F-0173-2025
potential to be contaminated with Listeria monocytogenes
Class IIFDA: TerminatedTreehouse Foods
FoodDec 4, 2024
Treehouse Foods GOOD & GATHER 12/9oz GRDL WFL MINI HSTYLE ORG-GDGTR UPC recall — FDA F-0206-2025
potential to be contaminated with Listeria monocytogenes
Class IIFDA: TerminatedTreehouse Foods
DrugDec 4, 2024
Neogen LICEOUT, Liquid Lice Treatment for Human Use, Contents: 128 FL OZ. (3785.4 mL mL) per recall — FDA D-0074-2025
CGMP violations.
Class IIFDA: OngoingNeogen Corporation
DrugDec 4, 2024
Unexo Life Sciences Private ABSORBINE JR PAIN RELIEVING KNEE PATCH, Camphor 7%, Menthol 7% recall — FDA D-0064-2025
cGMP Deviations
Class IIFDA: TerminatedUnexo Life Sciences Private Limited
DrugDec 4, 2024
Neogen LICEOUT, Liquid Lice Treatment for Human Use, Contents: 1 FL recall — FDA D-0073-2025
CGMP violations.
Class IIFDA: OngoingNeogen Corporation
DrugDec 4, 2024
THERACARE MAXIMUM STRENGTH PAIN RELIEF 4% LIDOCAINE PATCH, a) 1 patch recall — FDA D-0065-2025
cGMP Deviations
Class IIFDA: TerminatedUnexo Life Sciences Private Limited
VehicleDec 2, 2024
Model X headlights recall — NHTSA campaign 24V904000
Tesla, Inc. (Tesla) is recalling certain 2024 Model X vehicles. The parking lights and low beam headlights may flicker. As such, these vehicles fail to comply with the requirements of…
headlightsTesla, Inc.
Medical DeviceNov 27, 2024
Maquet Cardiovascular Acrobat-i Positioner recall — FDA Z-0484-2025
Deviations in the manufacturing process created a compromise in the sterile barrier, in which sterility cannot be assured during the duration of the product's 2-year shelf life.
Class IIFDA: OngoingMaquet Cardiovascular, LLC
Medical DeviceNov 27, 2024
Philips Medical Systems Technologies Vue PACS Diagnostic Viewer with Vue PACS client 12.1.5 recall — FDA Z-0497-2025
A software issue affecting Philips Vue PACS may cause incorrect ischemic map and table value calculations when using the export function in the Perfusion Application for a Siemens CT…
Class IIFDA: OngoingPhilips Medical Systems Technologies Ltd.
Medical DeviceNov 27, 2024
OrganOx metra -Intended as a Normothermic Machine Perfusion system of donor transport livers recall — FDA Z-0501-2025
Battery movement led to damage of one of the battery cells causing it to short to the battery retention bracket
Class IIFDA: OngoingOrganOx Ltd
Medical DeviceNov 27, 2024
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4484 recall — FDA Z-0380-2025
Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated…
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceNov 27, 2024
Alcon Research a) Alcon Custom-Pak CONSTELLATION 25G PLUS CHRISTIANA CARE HLTH SERV, # recall — FDA Z-0490-2025
Reported breakage in the tubing Anti-Reflux Valve (ARV) due to improper use. As a result, changes to labeling were made.
Class IIIFDA: OngoingAlcon Research LLC
Medical DeviceNov 27, 2024
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ recall — FDA Z-0374-2025
Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated…
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceNov 27, 2024
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number T5C4482 recall — FDA Z-0381-2025
Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated…
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceNov 27, 2024
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4483 recall — FDA Z-0376-2025
Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated…
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceNov 27, 2024
ETHICON MONOCRYL" (poliglecaprone 25) Suture REF Y936H MONOCRYL" Sutures are indicated for recall — FDA Z-0487-2025
Due a component mix-up in manufacturing, the affected products may contain incorrect needle type/size and suture length.
Class IIFDA: OngoingETHICON, Inc.
Medical DeviceNov 27, 2024
Hobbs Medical Posi-Stop Injection Needle, 23 Gauge recall — FDA Z-0470-2025
Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath…
Class IIFDA: OngoingHobbs Medical, Inc.
Medical DeviceNov 27, 2024
Biomet JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357 recall — FDA Z-0477-2025
Firm received complaints reporting that guides were warped when pulled out of packaging. This issue may result in extension of surgery to find another product, or may lead to adverse local…
Class IIFDA: OngoingBiomet, 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.