FoodJan 25, 2023
Sysco Merchandising and Supply Greco and Sons Dough Room Product No recall — FDA F-0301-2023
The dough ball products contain the undeclared allergen milk.
Class IFDA: TerminatedSysco Merchandising and Supply
Latest records
Latest recalls — page 632
The newest recall records with useful source details are listed here.
FoodJan 25, 2023
Sysco Merchandising and Supply Greco and Sons Dough Room Product No recall — FDA F-0296-2023
The dough ball products contain the undeclared allergen milk.
Class IFDA: TerminatedSysco Merchandising and Supply
FoodJan 25, 2023
Sysco Merchandising and Supply Greco and Sons Dough Room Product No recall — FDA F-0300-2023
The dough ball products contain the undeclared allergen milk.
Class IFDA: TerminatedSysco Merchandising and Supply
FoodJan 25, 2023
Caesar's Pasta Orefresco Pasta Manicotti Net Wt recall — FDA F-0308-2023
Possible contamination with Listeria monocytogenes in frozen manicotti pasta.
Class IIFDA: TerminatedCaesar's Pasta, LLC
FoodJan 25, 2023
Something South African Pepper Collection 8 Tube Gift Set - a colorful assortment of recall — FDA F-0263-2023
Due to presence of mold (Aspergillus brasiliensis) and Ochratoxin A.
Class IIFDA: TerminatedSomething South African LLC
DrugJan 25, 2023
Rasagiline Mesylate Tablets 1 mg recall — FDA D-0159-2023
Presence of Foreign Substance- A complaint was received of black spots/shiny metallic speck on the tablets.
Class IIFDA: TerminatedAscend Laboratories, LLC
DrugJan 25, 2023
MACLEODS PHARMA USA Levofloxacin Tablets, USP 500 mg recall — FDA D-0162-2023
Mismatching of the embossing on the tablets (T7) with the embossing mentioned in the package insert (ML63) in the distributed bottles.
Class IIIFDA: TerminatedMACLEODS PHARMA USA, Inc.
DrugJan 25, 2023
Sensorcaine recall — FDA D-0127-2023
Subpotent Drug: Testing results below the defined limit for the epinephrine portion of this product.
Class IIFDA: TerminatedFresenius Kabi USA, LLC
DrugJan 25, 2023
SENSORCAINE recall — FDA D-0129-2023
Subpotent Drug: Testing results below the defined limit for the epinephrine portion of this product.
Class IIFDA: TerminatedFresenius Kabi USA, LLC
DrugJan 25, 2023
Akorn Timolol Maleate Ophthalmic Solution, USP, 0.5% recall — FDA D-0156-2023
CGMP Deviations:
Class IIFDA: OngoingAkorn, Inc.
DrugJan 25, 2023
SINUVA (mometasone furoate) sinus implant, 1350 mcg, 1 implant per pouch recall — FDA D-0167-2023
Failed Dissolution Specification; product did not meet the average 24-hour drug release rate (dissolution) specification stability time point at 9 months.
Class IIIFDA: TerminatedIntersect ENT, Inc.
DrugJan 25, 2023
Fisher Scientific Co Hand Sanitizer, HSANI4LI, (Isopropyl Alcohol), 75% Topical Solution recall — FDA D-0164-2023
CGMP Deviations: Voluntary recall of all hand sanitizer distributed after March 31, 2022, due to FDA issued guidance to cease placing hand sanitizer product, produced under temporary…
Class IIFDA: OngoingFisher Scientific Co., LLC
DrugJan 25, 2023
Sensorcaine recall — FDA D-0128-2023
Subpotent Drug: Testing results below the defined limit for the epinephrine portion of this product.
Class IIFDA: TerminatedFresenius Kabi USA, LLC
DrugJan 25, 2023
Akorn Ketorolac Tromethamine Ophthalmic Solution, 0.5%, Packaged as a) 10 mL dropper bottle recall — FDA D-0141-2023
CGMP Deviations:
Class IIFDA: OngoingAkorn, Inc.
DrugJan 25, 2023
Southwest Iowa Renewable Energy SIREtizer Hand Sanitizer (Ethyl Alcohol) 80% recall — FDA D-0166-2023
CGMP Deviations and Superpotent Drug: Levels of acetal and acetaldehyde above allowable limits. Additionally, lot 001 was superpotent.
Class IIFDA: OngoingSouthwest Iowa Renewable Energy LLC
DrugJan 25, 2023
Accord Healthcare Daptomycin for Injection 350 mg/vial 1 Single-dose vial recall — FDA D-0131-2023
Labeling mixup: cartons labeled as Daptomycin 350 mg/vial were found to contain vials of Daptomycin 500 mg per vial
Class IFDA: TerminatedAccord Healthcare, Inc.
DrugJan 25, 2023
Fisher Scientific Co Hand Sanitizer, HSANI500ML, (Isopropyl Alcohol), 75% v/v recall — FDA D-0163-2023
CGMP Deviations: Voluntary recall of all hand sanitizer distributed after March 31, 2022, due to FDA issued guidance to cease placing hand sanitizer product, produced under temporary…
Class IIFDA: OngoingFisher Scientific Co., LLC
VehicleJan 23, 2023
Ford camera recall — NHTSA campaign 23V022000
Ford Motor Company (Ford) is recalling certain 2020-2023 Explorer, Lincoln Aviator, and 2020-2022 Lincoln Corsair vehicles equipped with a 360-degree camera. The video output may fail,…
cameraFord Motor Company
VehicleJan 19, 2023
Volvo Car USA hydraulic brakes recall — NHTSA campaign 23V012000
Volvo Car USA, LLC (Volvo Car) is recalling certain 2023 S60, V60, V60CC, V90CC, XC60, XC90, XC40, and C40 vehicles. A diagnostic error in the Brake Control Module 2 (BCM2) may cause a loss…
hydraulic brakesVolvo Car USA, LLC
VehicleJan 19, 2023
General Motors control/drive module recall — NHTSA campaign 23V013000
General Motors, LLC (GM) is recalling certain 2021-2022 Chevrolet Equinox and 2022 GMC Terrain vehicles. The fuel pump module may not consistently provide sufficient fuel to the engine,…
control/drive moduleGeneral Motors, LLC
Medical DeviceJan 18, 2023
Stradis Healthcare HCT CENTRAL LINE Insertion Tray, I2 per case recall — FDA Z-0940-2023
Potential for the outer bag having pinhole leaks near the seal, which may result in a breach in the sterility of the kit.
Class IIFDA: OngoingStradis Healthcare
Medical DeviceJan 18, 2023
Stradis Healthcare HCT 500mL BAGS, 2 Port, Sterile, Triple Packaged, 10 EVA BAGS/Pack, 7 recall — FDA Z-0936-2023
Potential for the outer bag having pinhole leaks near the seal, which may result in a breach in the sterility of the kit.
Class IIFDA: OngoingStradis Healthcare
Medical DeviceJan 18, 2023
Philips Garbin Ventilator, Model Number 1058180B recall — FDA Z-0884-2023
The replacement silicone sound abatement foam installed into some Trilogy 100 and Trilogy 200 devices may separate from the plastic backing to which it is attached. If this were to happen,…
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceJan 18, 2023
Philips Fetal Spiral Electrode-intended for patients requiring fetal heart rate monitoring recall — FDA Z-0908-2023
Fetal Spiral Electrode (FSE) spiral tip of the FSE breaking off during use and requiring surgical intervention to remove the broken tip from the neonate patient. Philips has decided to…
Class IIFDA: OngoingPhilips North America LLC
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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