FoodNov 1, 2023
Eagle Produce LLC, dba Martori Farms Whole cantaloupe, Brand name Kandy 11 count carton, 8 recall — FDA F-0298-2024
Possible contamination with Salmonella spp.
Class IFDA: TerminatedEagle Produce LLC, dba Martori Farms
Latest records
Latest recalls — page 492
The newest recall records with useful source details are listed here.
FoodNov 1, 2023
Betty Lou's Stabilyze Sugar Stable Dark Chocolate Peanut Butter, 50g recall — FDA F-0301-2024
Undeclared Sesame
Class IIFDA: TerminatedBetty Lou's Inc.
DrugNov 1, 2023
Methotrexate Tablets, USP, 2.5 mg, 10x10 Unit-Dose Tablets per carton recall — FDA D-0066-2024
Failed Tablet/Capsule Specifications: Tablets were observed to have an unsmooth surface with two tablets demonstrating illegible tablet identification and scoring.
Class IIIFDA: OngoingWest-Ward Columbus Inc.
DrugNov 1, 2023
Biomic Sciences, LLC dba ION Intelligence of ION* Sinus Support Nasal Spray, 1 fl oz/30 ml recall — FDA D-0068-2024
Microbial contamination of Non-Sterile Products
Class IIFDA: TerminatedBiomic Sciences, LLC dba ION Intelligence of Nature
VehicleOct 27, 2023
Mustang body control module/bcm recall — NHTSA campaign 23V727000
Ford Motor Company (Ford) is recalling certain 2020-2023 Mustang vehicles. The brake fluid level sensor may not activate the visual warning indicator when the brake fluid is low. As such,…
body control module/bcmFord Motor Company
VehicleOct 26, 2023
Highlander & Highlander Hybrid bumpers recall — NHTSA campaign 23V720000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2020-2023 Highlander & Highlander Hybrid vehicles. During normal vehicle operation, minor impact to the front lower…
bumpersToyota Motor Engineering & Manufacturing
VehicleOct 26, 2023
Forester engine and engine cooling recall — NHTSA campaign 23V723000
Subaru of America, Inc. (Subaru) is recalling certain 2024 Forester vehicles. The engine water pipe may have loose attachment bolts, allowing the pipe to lose its seal and leak coolant.
engine and engine coolingSubaru of America, Inc.
VehicleOct 26, 2023
Mazda North American Operations camera recall — NHTSA campaign 23V718000
Mazda North American Operations (Mazda) is recalling certain 2024 CX-90 and MAZDA3 vehicles. Due to a software error, the rearview, front, and/or side camera images may not appear on the…
cameraMazda North American Operations
Medical DeviceOct 25, 2023
North Coast Medical Gladiator, Wrist & Thumb Orthosis, Part Numbers: NC86650 (Small/Left) recall — FDA Z-0125-2024
The thumb strap of the wrist and thumb orthosis may contain latex that is not declared in the product labeling.
Class IIFDA: OngoingNorth Coast Medical Inc.
Medical DeviceOct 25, 2023
DeRoyal Head and Neck procedure kit, REF 89-4473, surgical convenience kit recall — FDA Z-0116-2024
DeRoyal is recalling certain lots of surgical procedure pack products that contain the B.Braun Medical Norm-Ject 2 Piece Syringe. The recall is due to the potential for the sterile…
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceOct 25, 2023
OLEA MEDICAL Functional MR V1.0 recall — FDA Z-0122-2024
When exporting regions of interest in DICOM SEGMENTATION format, when simultaneously exporting multiple volumes of interest, a functional magnetic resonance software bug may cause file…
Class IIFDA: OngoingOLEA MEDICAL
Medical DeviceOct 25, 2023
Access Vascular HydroPICC 5Fr Dual Lumen Maximal Barrier Kit, Product Model Number 80002004 recall — FDA Z-0115-2024
Specific lots of the Dual Lumen HydroPICC Kits were provided with the incorrect revision of the Instructions For Use (IFU) which do not include the following warnings statement: HydroPICC…
Class IIFDA: OngoingAccess Vascular, Inc.
Medical DeviceOct 25, 2023
Access Vascular HydroPICC 5Fr Dual Lumen, 80cm guidewire - Basic Kit, Product Model Number recall — FDA Z-0114-2024
Specific lots of the Dual Lumen HydroPICC Kits were provided with the incorrect revision of the Instructions For Use (IFU) which do not include the following warnings statement: HydroPICC…
Class IIFDA: OngoingAccess Vascular, Inc.
Medical DeviceOct 25, 2023
Cardinal Health 200 Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, Model recall — FDA Z-0112-2024
Syringe contains conical tip that is not compatible with certain needleless IV connector(s).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 25, 2023
Tornier stryker Tornier Perform Reversed Augmented Glenoid Lateralized Baseplate, 25mm recall — FDA Z-0113-2024
One lot of Tournier Perform Reversed Lateralized Baseplates were found to have been manufactured with 6mm spacers instead of 3mm spacers. This nonconformance prevents the central screw from…
Class IIFDA: OngoingTornier, Inc.
Medical DeviceOct 25, 2023
Olympus High-Flow Insufflation Unit, Model UHI-4 recall — FDA Z-0075-2024
There have been reports of patients suffering arrhythmias, reported as short cardiac arrests, during surgical procedures where UHI-4s were used. These events may have been due to an over…
Class IFDA: OngoingOlympus Corporation of the Americas
FoodOct 25, 2023
Moody Dunbar Sweet Potatoes sold under the brand names: HEB CUT SWEET recall — FDA F-0286-2024
During an internal investigation, the firm noticed that the Retort Chart was malfunctioning. No data was recorded during the production run.
Class IIFDA: OngoingMoody Dunbar Inc.
FoodOct 25, 2023
HEINZ Kraft Singles American Pasteurized Prepared Cheese product, 24 recall — FDA F-0296-2024
Plastic fragment. Product is recalled due to potential for a thin strip of the primary packaging film to remain adhered to the cheese slice after the wrapper has been removed.
Class IIFDA: CompletedHEINZ
FoodOct 25, 2023
Safeway Fresh Foods Sunnyside Farms, diced Organic Butternut Squash , 32-oz recall — FDA F-0295-2024
Safeway Fresh Foods of Vineland, NJ, is recalling its 32-oz. Diced Organic Butternut Squash product as it has the potential to be contaminated with Escherichia coli O45. The 32-oz. diced…
Class IIFDA: TerminatedSafeway Fresh Foods LLC
FoodOct 25, 2023
Sheng Kee of California, Inc dba Sheng Kee Small 12 -3 Flavor Assorted Mooncake Gift Box recall — FDA F-0288-2024
Undeclared allergen; egg.
Class IFDA: TerminatedSheng Kee of California, Inc dba Sheng Kee Bakery
DrugOct 25, 2023
Bupropion Hydrochloride Extended-Release Tablets USP (SR), 150 mg, 60 tablets bottle recall — FDA D-0044-2024
Failed Dissolution Specifications
Class IIIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugOct 25, 2023
Imprimis NJOF MYDRIATIC-4: Tropicamide - Proparacaine - Phenylephrine - Ketorolac Sterile recall — FDA D-0043-2024
Subpotent: Out of Specification result observed for Ketorolac assay levels, below the 90.0-110.0% of label claim.
Class IIIFDA: TerminatedImprimis NJOF, LLC
DrugOct 25, 2023
Church & Dwight TheraBreath for Kids! Oral Rinse, sodium fluoride 0.05% recall — FDA D-0046-2024
Microbial contamination of Non-Sterile Product; presence of yeast identified as Candida parapsilosis
Class IFDA: OngoingChurch & Dwight Inc.
DrugOct 25, 2023
Betaxolol Tablets, USP 10 mg recall — FDA D-0049-2024
Presence of Foreign Tablets/Capsules: There is a potential presence of oxycodone HCl tablets, USP 5 mg in bottles.
Class IFDA: TerminatedKVK-Tech, Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026364 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