FoodOct 29, 2025
SNO PAC FOODS Frozen Organic Spinach Net Wt recall — FDA H-0109-2026
Organic Spinach has the potential to be contaminated with Listeria monocytogenes.
Class IIFDA: TerminatedSNO PAC FOODS INC
Latest records
Latest recalls — page 154
The newest recall records with useful source details are listed here.
FoodOct 29, 2025
Albertsons Companies Ready Meals Smoked Mozzarella With Hot Links Extra Large, UPC recall — FDA H-0124-2026
Listeria monocytogenes. Albertson's store-made deli items contain a recalled Penne pasta ingredient which was recalled due to Listeria monocytogenes.
Class IFDA: TerminatedAlbertsons Companies LLC
FoodOct 29, 2025
Reser's Fine Foods Fresh Creative Foods recall — FDA H-0090-2026
Salad Kits are recalled due to potential contamination with Listeria monocytogenes.
Class IFDA: TerminatedReser's Fine Foods, Inc.
DrugOct 29, 2025
Ketorolac Tromethamine Injection, USP, 60 mg/2 mL (30 mg/mL), 2 mL Single-Dose Vial, For recall — FDA D-0036-2026
Presence of Particulate Matter: Particulate matter identified as glass
Class IIFDA: OngoingAspiro Pharma Limited
DrugOct 29, 2025
ZICAM COLD REMEDY MEDICATED FRUIT DROPS - ELDERBERRY ZICAM" MEDICATED FRUIT DROPS ELDERBERRY recall — FDA D-0095-2026
Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient.
Class IIFDA: OngoingChurch & Dwight Co., Inc.
DrugOct 29, 2025
Cetirizine Hydrochloride Tablets USP 10 mg, 500 Tablets bottles recall — FDA D-0033-2026
Tablet/Capsules Imprinted with Wrong ID
Class IIIFDA: OngoingJB Chemicals and Pharmaceuticals Ltd
DrugOct 29, 2025
Gabapentin Capsules, USP, 100 mg, 100 Capsules (10 x 10 blister packs) recall — FDA D-0030-2026
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
Class IIFDA: OngoingThe Harvard Drug Group LLC
DrugOct 29, 2025
Medline Industries Medline, Alcohol Prep Pads recall — FDA D-0035-2026
Subpotent Drug
Class IIFDA: OngoingMedline Industries, LP
DrugOct 29, 2025
USV Private Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 %, 5 mL (0.17 FL OZ) recall — FDA D-0034-2026
Failed Impurities/Degradation Specifications: The result for 'Any individual unspecified impurity' exceeds the specification limit.
Class IIFDA: OngoingUSV Private Limited
DrugOct 29, 2025
Cetirizine Hydrochloride Tablets USP 10 mg, 100 Tablets bottles recall — FDA D-0032-2026
Tablet/Capsules Imprinted with Wrong ID
Class IIIFDA: OngoingJB Chemicals and Pharmaceuticals Ltd
DrugOct 29, 2025
Gabapentin Capsules, USP, 100 mg, 10 Capsules (10 x 1 blister pack) recall — FDA D-0031-2026
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
Class IIFDA: OngoingThe Harvard Drug Group LLC
VehicleOct 24, 2025
Ford windshield recall — NHTSA campaign 25V730000
Ford Motor Company (Ford) is recalling certain 2025-2026 Lincoln Corsair, Lincoln Aviator, and Explorer vehicles. The windshield glass may have visible air bubbles, which can obscure the…
windshieldFord Motor Company
VehicleOct 24, 2025
Ford sunroof recall — NHTSA campaign 25V729000
Ford Motor Company (Ford) is recalling certain 2021-2022 Expedition, Lincoln Navigator, 2021-2023 F-150, 2022 F-250 SD, F-350 SD, and F-450 SD vehicles. The moonroof wind deflector clips…
sunroofFord Motor Company
VehicleOct 23, 2025
Bronco critical fasteners recall — NHTSA campaign 25V721000
Ford Motor Company (Ford) is recalling certain 2021-2023 Bronco vehicles. The front seats may have a loose or dislodged seat frame height-adjust pivot bolt.
critical fastenersFord Motor Company
VehicleOct 23, 2025
Ram ProMaster radiator recall — NHTSA campaign 25V720000
Chrysler (FCA US, LLC) is recalling certain 2018-2026 Ram ProMaster vehicles. The electrical circuit for the radiator fan may overheat.
radiatorChrysler (FCA US, LLC)
Medical DeviceOct 22, 2025
Baxter Healthcare CLEARLINK SYSTEM Solution Set, Non-Vented, two CLEARLINK Luer Activated recall — FDA Z-0191-2026
IV sets may leak.
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceOct 22, 2025
MICROVENTION Flow Re-Direction Endoluminal Devices: FRED 27, REF: FRED5019, FRED5029 recall — FDA Z-0108-2026
Flow diverter may have a manufacturing issue related to the tantalum length and/or tantalum attachment pattern, which may lead the device to be incompletely open or not properly apposed to…
Class IIFDA: OngoingMICROVENTION Inc.
Medical DeviceOct 22, 2025
Boston Scientific ACCOLADE DR SL MRI (Model L311) recall — FDA Z-0082-2026
Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family…
Class IFDA: OngoingBoston Scientific Corporation
Medical DeviceOct 22, 2025
Baxter Healthcare CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard recall — FDA Z-0199-2026
IV sets may leak.
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceOct 22, 2025
Boston Scientific Model Number S722, ALTRUA 2 DR EL Pacemaker recall — FDA Z-0100-2026
Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family…
Class IFDA: OngoingBoston Scientific Corporation
Medical DeviceOct 22, 2025
American Contract Systems Medical convenience kits Item Number/Description RCGY52D GYN recall — FDA Z-0179-2026
Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been…
Class IIFDA: OngoingAmerican Contract Systems Inc.
Medical DeviceOct 22, 2025
Boston Scientific PROPONENT DR SL (Model L201) recall — FDA Z-0086-2026
Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family…
Class IFDA: OngoingBoston Scientific Corporation
Medical DeviceOct 22, 2025
American Contract Systems Medical convenience kits Item Number/Description UICL44P ADULT recall — FDA Z-0177-2026
Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been…
Class IIFDA: OngoingAmerican Contract Systems Inc.
Medical DeviceOct 22, 2025
BioPro Femoral Head (Ceramic heads 28-30) Product ID/Description 19023 HEAD FEMORAL CERAMIC recall — FDA Z-0151-2026
Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.
Class IIFDA: OngoingBioPro, Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026300 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories