FoodMar 15, 2023
Sunny Dell Rao's Homemade Roasted Peppers with Portobello Mushrooms Net recall — FDA F-0406-2023
May contain undeclared pine nuts
Class IIFDA: TerminatedSunny Dell, Inc.
Latest records
Latest recalls — page 610
The newest recall records with useful source details are listed here.
FoodMar 15, 2023
Titans Global JSJ ZSR Cake 3.35 oz recall — FDA F-0411-2023
Product was found to have the presence of egg, which is not declared on the label.
Class IFDA: TerminatedTitans Global Inc.
FoodMar 15, 2023
DAILY HARVEST Item ID L02-VEGBN, Net Wt recall — FDA F-0419-2023
Product is linked to complaints of gastrointestinal illness.
Class IIFDA: TerminatedDAILY HARVEST
FoodMar 15, 2023
4 Earth Farms formerly Mcl Fresh Brussel Sprouts 98.5% of product was packaged for retail recall — FDA F-0414-2023
Organic Brussel Sprouts tested positive for Chlorpyrifos by the State of California
Class IIIFDA: Terminated4 Earth Farms formerly Mcl Fresh Inc.
FoodMar 15, 2023
Titans Global JSJ DMC Leaf Cake 3.35 oz recall — FDA F-0412-2023
Product was found to have the presence of egg, which is not declared on the label.
Class IFDA: TerminatedTitans Global Inc.
FoodMar 15, 2023
Chukar Cherry Company item #21508, net wt recall — FDA F-0417-2023
undeclared hazelnuts
Class IFDA: TerminatedChukar Cherry Company Inc.
DrugMar 15, 2023
Amerisource Health Services Verapamil Hydrochloride Extended-Release Tablets, USP, 120 mg recall — FDA D-0436-2023
Failed Dissolution Specification: Out of specification dissolution results at time point zero. The OOS was above specified values.
Class IIFDA: TerminatedAmerisource Health Services LLC
DrugMar 15, 2023
Nutraceutical NaturalCare, children's, Allergy Care, Homeopathic, 4 Months and Up, Liquid recall — FDA D-0440-2023
CGMP Deviations: Raw material recalled by repackager, due to discoloration.
Class IIFDA: OngoingNutraceutical Corporation
DrugMar 15, 2023
Teva Pharmaceuticals USA Metformin hydrochloride Extended-Release Tablets, 1000 mg, 60-count recall — FDA D-0441-2023
CGMP Deviations: Detection of N-Nitrosodimethylamine (NDMA) levels in excess of the Acceptable Daily Intake Limit.
Class IIFDA: TerminatedTeva Pharmaceuticals USA Inc.
DrugMar 15, 2023
Nutraceutical NatraBio, Cold& Sinus Nasal Spray, Homeopathic Medicine, 0.8 FL Oz. ( 24ml) recall — FDA D-0438-2023
CGMP Deviations: Raw material recalled by repackager, due to discoloration.
Class IIFDA: OngoingNutraceutical Corporation
DrugMar 15, 2023
Pharmedica USA Purely Soothing 15% MSM Drops recall — FDA D-0456-2023
Non-Sterility
Class IFDA: OngoingPharmedica USA, LLC
DrugMar 15, 2023
Brimonidine Tartrate Ophthalmic Solution 0.15% recall — FDA D-0433-2023
Lack of sterility assurance: Cracks have developed in some of the units caps of Brimonidine tartrate ophthalmic solution bottles. There is a possibility the broken cap may impact sterility.
Class IIFDA: CompletedApotex Corp.
DrugMar 15, 2023
Nanomaterials Discovery Snowy Range Blue Alcohol Antiseptic 80% Topical Solution Hand recall — FDA D-0455-2023
Chemical Contamination: FDA analysis found the product to contain methanol, acetaldehyde, and acetal above the limits.
Class IFDA: OngoingNanomaterials Discovery Corporation
VehicleMar 10, 2023
Maverick tail lights recall — NHTSA campaign 23V160000
Ford Motor Company (Ford) is recalling certain 2023 Maverick vehicles. A missing electrical circuit may cause the trailer taillights to not illuminate as intended when utilizing the vehicle…
tail lightsFord Motor Company
VehicleMar 10, 2023
Bronco camera recall — NHTSA campaign 23V165000
Ford Motor Company (Ford) is recalling certain 2021-2022 Bronco vehicles equipped with 8-inch SYNC infotainment screens that were previously remedied under recall 22V-825. The rearview…
cameraFord Motor Company
VehicleMar 10, 2023
F-150 linkages recall — NHTSA campaign 23V163000
Ford Motor Company (Ford) is recalling certain 2021 F-150 vehicles. The windshield wiper arms may break, causing the windshield wipers to fail.
linkagesFord Motor Company
VehicleMar 9, 2023
Honda buckle recall — NHTSA campaign 23V158000
Honda (American Honda Motor Co.) is recalling certain 2017-2020 CR-V, 2018-2019 Accord and Accord Hybrid, 2018-2020 Odyssey, 2019 Insight, and 2019-2020 Acura RDX vehicles. A manufacturing…
buckleHonda (American Honda Motor Co.)
Medical DeviceMar 8, 2023
Covidien Surgipro Monofilament Polypropylene Sutures Product Description CP-535 SURGIPRO* 1 recall — FDA Z-1179-2023
Sterile Barrier Breach of Breather Pouch may cause infection or vision loss for ophthalmic procedures in cases where there is direct patient contact
Class IIFDA: OngoingCovidien, LP
Medical DeviceMar 8, 2023
Beaver Visitec International CustomEyes kits recall — FDA Z-1200-2023
Device packaging may contain open seals, compromising product sterility.
Class IIFDA: OngoingBeaver Visitec International, Inc.
Medical DeviceMar 8, 2023
Unetixs Vascular MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic device recall — FDA Z-1194-2023
The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism.
Class IIFDA: OngoingUnetixs Vascular, Inc.
Medical DeviceMar 8, 2023
Covidien Novafil Monofilament Polybutester Suture Product Description: 8886 4002-41 NOVAFIL recall — FDA Z-1175-2023
Sterile Barrier Breach of Breather Pouch may cause infection or vision loss for ophthalmic procedures in cases where there is direct patient contact
Class IIFDA: OngoingCovidien, LP
Medical DeviceMar 8, 2023
Wright Medical Technology ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 402S0425, Bone recall — FDA Z-1169-2023
Stryker has identified an issue that impacts two specific lots of CLAW" II plates. The plates within these two lots were found to have been comingled, resulting in the incorrect product in…
Class IIFDA: OngoingWright Medical Technology, Inc.
Medical DeviceMar 8, 2023
Unetixs Vascular MultiLab Series II REVO non-invasive vascular diagnostic device, Model recall — FDA Z-1196-2023
The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism.
Class IIFDA: OngoingUnetixs Vascular, Inc.
Medical DeviceMar 8, 2023
stryker Hoffmann LRF, Transport Strut, Model Number 4933-0-400 recall — FDA Z-1191-2023
Stryker has identified a nonconformance in specific lots of Hoffmann LRF Bone Transport Struts. Specifically, the thread pitch is oversized at the distal end of the threaded rod, and as a…
Class IIFDA: OngoingStryker GmbH
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026110 records · 3 categoriesSeptember 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 categories