FoodMar 4, 2020
Pro-Form Manufacturing Lifetime Fitness D recall — FDA F-0784-2020
Notified by supplier that flax seed used in products is under recall due to detection of unapproved herbicide.
Class IIIFDA: TerminatedPro-Form Manufacturing LLC
Monthly breakdown
2020 recalls by month
Select a month to review the recall records reported during that period.
December 2020315 records · 4 categoriesNovember 2020241 records · 4 categoriesOctober 2020416 records · 4 categoriesSeptember 2020371 records · 4 categoriesAugust 2020245 records · 4 categoriesJuly 2020442 records · 4 categoriesJune 2020342 records · 4 categoriesMay 2020315 records · 4 categoriesApril 2020422 records · 4 categoriesMarch 2020368 records · 4 categoriesFebruary 2020551 records · 4 categoriesJanuary 2020224 records · 4 categories
2020 recalls — page 145
Records are ordered by the best available source date.
FoodMar 4, 2020
Pro-Form Manufacturing Nature's Sunshine NutriSmart Mezcla en polvo a base de recall — FDA F-0781-2020
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
Salud Natural Entrepreneur Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 recall — FDA F-0756-2020
FDA sampling of senna leaves powder, an ingredient used to manufacture the Nopalina Flax Seed Fiber (powder) and Nopalina Flax Seed Fiber (capsules), tested positive for three types of…
Class IFDA: TerminatedSalud Natural Entrepreneur, Inc.
FoodMar 4, 2020
Salud Natural Entrepreneur Nopalina Flax Seed Fiber in 1 and 2 lb bags, UPC 8 90523 00072 recall — FDA F-0755-2020
FDA sampling of senna leaves powder, an ingredient used to manufacture the Nopalina Flax Seed Fiber (powder) and Nopalina Flax Seed Fiber (capsules), tested positive for three types of…
Class IFDA: TerminatedSalud Natural Entrepreneur, Inc.
FoodMar 4, 2020
Lanvin French Bakery Deep-fried Bread recall — FDA F-0739-2020
Undeclared wheat and soybean oil.
Class IIFDA: TerminatedLanvin French Bakery, LLC
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
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
About the 2020 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.