FoodNov 27, 2024
Grand Central Bakery FRE Co U-BAKE Marionberry Pie, frozen product and packaged in LDPE recall — FDA F-0219-2025
Undeclared egg
Class IFDA: TerminatedGrand Central Bakery FRE Co Inc.
November 2024 recalls — page 3
These records include useful source details for the selected month.
FoodNov 27, 2024
Grand Central Bakery FRE Co U-BAKE Chicken Pot Pie, frozen product and packaged in recall — FDA F-0220-2025
Undeclared egg
Class IFDA: TerminatedGrand Central Bakery FRE Co Inc.
VehicleNov 27, 2024
Chrysler side/window recall — NHTSA campaign 24V897000
Chrysler (FCA US, LLC) is recalling certain 2022-2024 Jeep Grand Cherokee and 2021-2024 Jeep Grand Cherokee L vehicles. An improperly secured connector for the front seat side air bags…
side/windowChrysler (FCA US, LLC)
VehicleNov 27, 2024
Honda filler pipe and cap recall — NHTSA campaign 24V900000
Honda (American Honda Motor Co.) is recalling certain 2023-2024 Passport and 2023-2025 Pilot vehicles. The fuel filler neck tube and fuel filler pipe may separate, allowing fuel to leak.
filler pipe and capHonda (American Honda Motor Co.)
DrugNov 27, 2024
Lisinopril Tablets, USP 10 mg, 90 tablets per bottle recall — FDA D-0061-2025
Presence of Foreign Object: A pharmacist discovered a metal fragment embedded in a lisinopril 10 mg tablet.
Class IIFDA: TerminatedEvaric Pharmaceuticals Inc.
DrugNov 27, 2024
Xelstrym (dextroamphetamine) transdermal system, 13.5 mg dextroamphetamine/9 hours, 30 recall — FDA D-0055-2025
Defective Delivery System: The product does not meet predetermined specifications for Coldflow (adhesive).
Class IIFDA: OngoingNoven Pharmaceuticals Inc
DrugNov 27, 2024
Ramipril Capsules USP 5 mg, a) 90 count (NDC 68180-590-09), b) 100 count NDC 68180-590-01) recall — FDA D-0053-2025
CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugNov 27, 2024
Ramipril Capsules USP 2.5 mg, a) 90 count (NDC 68180-589-09), b) 100 count NDC recall — FDA D-0052-2025
CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugNov 27, 2024
Ramipril Capsules USP 10 mg, a) 90 count (NDC 68180-591-09), b) 100 count NDC 68180-591-01) recall — FDA D-0054-2025
CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugNov 27, 2024
Padagis US Triamcinolone Acetonide Cream USP, 0.025%, 1 LB (454 g) per jar recall — FDA D-0048-2025
Subpotent and Superpotent Drug. Out of specification assay results recorded as part of Uniformity of Container test during long-term stability testing.
Class IIIFDA: TerminatedPadagis US LLC
VehicleNov 22, 2024
Model Y recliner recall — NHTSA campaign 24V886000
Tesla, Inc. (Tesla) is recalling certain 2024 Model Y vehicles. The weld attaching the seat recliner mechanism to the front seat backs may fail.
reclinerTesla, Inc.
VehicleNov 21, 2024
Hyundai Motor camera recall — NHTSA campaign 24V879000
Hyundai Motor America (Hyundai) is recalling certain 2021-2022 Santa Fe, Santa Fe HEV, Elantra, Elantra HEV and 2022 Elantra N and Santa Fe PHEV vehicles. Due to a damaged printed circuit…
cameraHyundai Motor America
VehicleNov 21, 2024
Toyota Motor Engineering & Manufacturing steering recall — NHTSA campaign 24V878000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2023-2024 Corolla and Corolla Hybrid vehicles. Due to cracks developed during the manufacturing process, the steering…
steeringToyota Motor Engineering & Manufacturing
Medical DeviceNov 20, 2024
AVID Medical Halyard EP PACK - Medical convenience kits recall — FDA Z-0439-2025
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site…
Class IIFDA: OngoingAVID Medical, Inc.
Medical DeviceNov 20, 2024
MEDLINE INDUSTRIES, LP - Northfield URINALYSIS KIT 4, SKU DYLAB1021 recall — FDA Z-0357-2025
Specimen container included in kits is labeled as sterile, but has been identified to be non-sterile. Long-term consequences may include unnecessary treatment and/or prolonged…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceNov 20, 2024
Medtronic Recharger Kits, RS6230, RS7230, and RS5220A, containing components WR9230 and recall — FDA Z-0372-2025
The Wireless Rechargers in the kits may be unable to enter a recharging session upon first use.
Class IIFDA: OngoingMedtronic Neuromodulation
Medical DeviceNov 20, 2024
Getinge Usa Sales MEERA CL mobile operating table - Designed for the placement and recall — FDA Z-0459-2025
Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via…
Class IIFDA: OngoingGetinge Usa Sales Inc.
Medical DeviceNov 20, 2024
The Metrix Company SECURE 1000 mL EMPTY EVA CONTAINER With 2 Ports, REF 66055 recall — FDA Z-0341-2025
A limited number of IV bags have been found to leak during filling.
Class IIFDA: OngoingThe Metrix Company
Medical DeviceNov 20, 2024
AVID Medical Halyard LAPAROSCOPY TRAY - Medical convenience kits recall — FDA Z-0404-2025
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site…
Class IIFDA: OngoingAVID Medical, Inc.
Medical DeviceNov 20, 2024
Getinge Usa Sales MEERA CL mobile operating table - Designed for the placement and recall — FDA Z-0457-2025
Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via…
Class IIFDA: OngoingGetinge Usa Sales Inc.
Medical DeviceNov 20, 2024
AVID Medical Halyard GYN PAC - Medical convenience kits recall — FDA Z-0436-2025
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site…
Class IIFDA: OngoingAVID Medical, Inc.
Medical DeviceNov 20, 2024
Philips Zenition 70 recall — FDA Z-0353-2025
Potential for the Mains Control Unit board fuse may blow out during system start-up or during a procedure.
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceNov 20, 2024
AVID Medical Halyard HEART CATH LAB PK, STRL F G - Medical convenience kits recall — FDA Z-0418-2025
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site…
Class IIFDA: OngoingAVID Medical, Inc.
Medical DeviceNov 20, 2024
AVID Medical Halyard C SECTION BUNDLE - Medical convenience kits recall — FDA Z-0406-2025
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site…
Class IIFDA: OngoingAVID Medical, Inc.
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.