FoodMar 4, 2020
Pro-Form Manufacturing Lifetime Fitness D recall — FDA F-0783-2020
Notified by supplier that flax seed used in products is under recall due to detection of unapproved herbicide.
Class IIIFDA: TerminatedPro-Form Manufacturing LLC
Latest records
Latest recalls — page 1069
The newest recall records with useful source details are listed here.
FoodMar 4, 2020
Losurdo Foods 1 recall — FDA F-0751-2020
The firm is recalling the product as a precautionary measure due to a production employee that handled the product being diagnosed with food poisoning two days after the production run…
Class IIFDA: TerminatedLosurdo Foods, Inc.
FoodMar 4, 2020
Pro-Form Manufacturing Nature's Sunshine NutriSmart Polvo Para Preparar Bebida Sabor recall — FDA F-0779-2020
Notified by supplier that flax seed used in products is under recall due to detection of unapproved herbicide.
Class IIIFDA: TerminatedPro-Form Manufacturing LLC
FoodMar 4, 2020
Bakkavor Foods USA chef's recipe MUSHROOM BARLEY SOUP NET WT 16 OZ recall — FDA F-0798-2020
The product contains undeclared milk.
Class IFDA: TerminatedBakkavor Foods USA Inc.
FoodMar 4, 2020
Lotte Int'l 12 pack, 11.85 oz recall — FDA F-0752-2020
FDA testing found almond protein in the products, which is not an ingredient in the product.
Class IIFDA: TerminatedLotte Int'l America Corp.
FoodMar 4, 2020
Domino Foods 50 LB bag, UPC 049200009727, Lots 50044 recall — FDA F-0746-2020
Possible foreign material.
Class IIFDA: TerminatedDomino Foods Inc.
FoodMar 4, 2020
PNW Veg Co Foodservice item, Norpac Catalog Number 08099, frozen recall — FDA F-0742-2020
FLAV-R-PAC Roasted Spicy Potatoes Obrien was recalled due to undeclared wheat and soy.
Class IFDA: TerminatedPNW Veg Co LLC
FoodMar 4, 2020
Great Lakes Cheese Co Coburn Farms Snackers, Sharp Yellow Cheddar Cheese, Cherry recall — FDA F-0800-2020
Coburn Farms 4.5oz Snackers is being recalled due to a labeling error leading to undeclared peanut.
Class IIFDA: TerminatedGreat Lakes Cheese Co Inc.
FoodMar 4, 2020
Lanvin French Bakery Deep-fried Donut recall — FDA F-0738-2020
Undeclared wheat and soybean oil.
Class IIFDA: TerminatedLanvin French Bakery, LLC
DrugMar 4, 2020
Breckenridge Pharmaceutical Zoledronic Acid Injection 5 mg/100 mL (0.05 mg/mL), Solution for recall — FDA D-1063-2020
Failed Impurities/Degradation Specifications: Out-of-specification results obtained for impurities during stability testing.
Class IIIFDA: TerminatedBreckenridge Pharmaceutical, Inc.
DrugMar 4, 2020
Akorn Sodium Chloride Ophthalmic Ointment USP, 5%, 3.5 g tubes recall — FDA D-0859-2020
Presence of Particulate Matter: Brown spots observed on the inside of the tube of product, identified as tin with trace copper, which are the base of the materials of construction for the…
Class IIIFDA: TerminatedAkorn, Inc.
DrugMar 4, 2020
Golden State Medical Supply TRAMADOL HYDROCHLORIDE Tablets, USP, 50 mg recall — FDA D-0856-2020
Labeling: Incorrect package insert - Patient leaflets for the specified lots of unscored tablets contain language relative to a 25 mg dosing titration that necessitates the use of a scored…
Class IIIFDA: TerminatedGolden State Medical Supply Inc.
DrugMar 4, 2020
Akorn CVS Health Sodium Chloride Ophthalmic Ointment USP, 5%, 3.5 g tubes recall — FDA D-0861-2020
Presence of Particulate Matter: Brown spots observed on the inside of the tube of product, identified as tin with trace copper, which are the base of the materials of construction for the…
Class IIIFDA: TerminatedAkorn, Inc.
DrugMar 4, 2020
Akorn Well at Walgreens Sodium Chloride Ophthalmic Ointment USP, 5%, 3.5 g tubes recall — FDA D-0860-2020
Presence of Particulate Matter: Brown spots observed on the inside of the tube of product, identified as tin with trace copper, which are the base of the materials of construction for the…
Class IIIFDA: TerminatedAkorn, Inc.
DrugMar 4, 2020
Phenytoin Oral Suspension USP, 125 mg/5 mL potency, 8 fl oz (237 mL) recall — FDA D-0863-2020
Resuspension Problems: Two lots of Phenytoin Oral Suspension USP 125mg/5mL may coagulate and may not resuspend as per the label copy instructions.
Class IFDA: TerminatedTaro Pharmaceuticals U.S.A., Inc.
VehicleMar 3, 2020
Chrysler clutch recall — NHTSA campaign 20V124000
Chrysler (FCA US LLC) is recalling certain 2018-2020 Jeep Wrangler and 2020 Gladiator vehicles equipped with manual transmissions. The clutch pressure plate may overheat and fracture.
clutchChrysler (FCA US LLC)
VehicleFeb 28, 2020
Sonata labels recall — NHTSA campaign 20V122000
Hyundai Motor America (Hyundai) is recalling certain 2020 Sonata vehicles produced between October 22, 2019 and February 13, 2020. The tire pressure label inside the driver's door and the…
labelsHyundai Motor America
Medical DeviceFeb 26, 2020
Covidien Polysorb Braided Absorbable Suture 1 36 VIOLET GS-21, Item Code CL925 - Product recall — FDA Z-1284-2020
There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
Class IIFDA: TerminatedCovidien LLC
Medical DeviceFeb 26, 2020
Abbott Vascular NC TREK Coronary Dilatation Catheter, REF 1012453-15 Rx Only, NC TREK RX recall — FDA Z-1130-2020
Coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
Class IFDA: TerminatedAbbott Vascular
Medical DeviceFeb 26, 2020
Abbott Vascular NC TREK Coronary Dilatation Catheter, REF 1012455-15 Rx Only,NC TREK RX 5.00 recall — FDA Z-1138-2020
Coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
Class IFDA: TerminatedAbbott Vascular
Medical DeviceFeb 26, 2020
Nobel Biocare Usa Drill Tapered RP 4.3x13 mm Single-Pat - Product Usage: The Guided Drills recall — FDA Z-1310-2020
Due to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall remain…
Class IIFDA: TerminatedNobel Biocare Usa LLC
Medical DeviceFeb 26, 2020
Nobel Biocare Usa Implant Retrieval Instrument Tri Channel 6.0 22 mm - Product Usage: They recall — FDA Z-1321-2020
Due to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall remain…
Class IIFDA: TerminatedNobel Biocare Usa LLC
Medical DeviceFeb 26, 2020
Abbott Vascular NC TREK Coronary Dilatation Catheter, REF 1012455-12 Rx Only, NC TREK RX recall — FDA Z-1137-2020
Coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
Class IFDA: TerminatedAbbott Vascular
Medical DeviceFeb 26, 2020
Nobel Biocare Usa Abutment Screw Retrieval Instrument RP/WP/6.0 - Product Usage: The recall — FDA Z-1325-2020
Due to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall remain…
Class IIFDA: TerminatedNobel Biocare Usa LLC
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026180 records · 4 categoriesSeptember 2026363 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