FoodOct 16, 2019
Lion Foods Greenland All Natural Gourmet Crispy Fried Onions NET WT 400g recall — FDA F-0024-2020
Potential metal contamination
Class IIFDA: TerminatedLion Foods
Monthly breakdown
2019 recalls by month
Select a month to review the recall records reported during that period.
December 2019321 records · 4 categoriesNovember 2019597 records · 4 categoriesOctober 2019525 records · 4 categoriesSeptember 2019268 records · 4 categoriesAugust 2019505 records · 4 categoriesJuly 2019680 records · 4 categoriesJune 2019445 records · 4 categoriesMay 2019396 records · 4 categoriesApril 2019242 records · 4 categoriesMarch 2019250 records · 4 categoriesFebruary 2019381 records · 4 categoriesJanuary 2019142 records · 4 categories
2019 recalls — page 47
Records are ordered by the best available source date.
FoodOct 16, 2019
SONORA MILLS FOODS INC DBA POPCH Popchips Sea Salt Potato Popped Chips recall — FDA F-0026-2020
Some batches of PopChips may contain gluten levels that exceed the firms specification.
Class IIFDA: TerminatedSONORA MILLS FOODS INC DBA POPCH
FoodOct 16, 2019
STARK Ritter Sport KAFFEESPLITTER Chocolate with caramelized coffee recall — FDA F-0021-2020
Product contains undeclared milk.
Class IIFDA: TerminatedSTARK Inc.
FoodOct 16, 2019
Diamond Crystal Brands Madrona Market Delicatessen Hot Cocoa Mix, Net Wt recall — FDA F-0030-2020
Products were made with a cocoa powder that contained soy lecithin but soy was not declared on the label.
Class IIFDA: TerminatedDiamond Crystal Brands Inc.
FoodOct 16, 2019
Vinh Sanh Trading Tep Say Crispy Tiny Shrimp Snack, Net Wt recall — FDA F-0033-2020
Undeclared sulfites.
Class IIFDA: TerminatedVinh Sanh Trading Corp
FoodOct 16, 2019
Sara Lee Frozen Bakery Chef Pierre ¿ SMALL WHOLE GRAIN BANANA MUFFINS NET WT 12 LB recall — FDA F-0040-2020
The firm was notified from a consumer of foreign material in the product. After examination they discovered that the foreign material was "tree nut".
Class IFDA: CompletedSara Lee Frozen Bakery
FoodOct 16, 2019
Diamond Crystal Brands Chef's Companion Instant Chocolate Mousse Mix Net Wt recall — FDA F-0031-2020
Products were made with a cocoa powder that contained soy lecithin but soy was not declared on the label.
Class IIFDA: TerminatedDiamond Crystal Brands Inc.
FoodOct 16, 2019
Consider Bardwell Farm brand Experience Handmade Cow Cheese recall — FDA F-0039-2020
Products may be contaminated with Listeria monocytogenes
Class IFDA: TerminatedConsider Bardwell Farm, LLC
FoodOct 16, 2019
SONORA MILLS FOODS INC DBA POPCH Popchips Sour Cream & Onion Potato Popped Chips recall — FDA F-0027-2020
Some batches of PopChips may contain gluten levels that exceed the firms specification.
Class IIFDA: TerminatedSONORA MILLS FOODS INC DBA POPCH
DrugOct 16, 2019
Unipharma, LLC DrKids Children's Natural Cough Syrup English Ivy Leaf recall — FDA D-0132-2020
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Class IIFDA: TerminatedUnipharma, LLC.
DrugOct 16, 2019
Optiray 320 (ioversol) Injection 68%, 320 mg/mL Organically Bound Iodine recall — FDA D-0137-2020
Labeling: Not Elsewhere Classified: RFID formatting error which reads product in Ultraject syringe as expired and will not allow injection of product by the Optivantage injector.
Class IIFDA: TerminatedGUERBET LLC
DrugOct 16, 2019
Benazepril HCl Tablets, USP 40 mg, 100 count bottles recall — FDA D-0134-2020
Presence of Foreign Tablet/Capsule; Promethazine HCl tablet found in the Benazepril HCl bottle
Class IIIFDA: TerminatedAmneal Pharmaceuticals, Inc.
DrugOct 16, 2019
Morton Grove Pharmaceuticals Prednisolone Sodium Phosphate Oral Solution, 15 mg/5 mL recall — FDA D-0130-2020
Failed Impurities/Degradation Specifications - failed specs for Prednisolone Impurity 14
Class IIFDA: TerminatedMorton Grove Pharmaceuticals, Inc.
DrugOct 16, 2019
Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 240 mg, 30 count bottle recall — FDA D-0131-2020
GMP Deviation: lot not intended for commercial distribution.
Class IIIFDA: TerminatedTeva Pharmaceuticals USA
DrugOct 16, 2019
Estradiol tablets, 0.5 mg, 100-count bottles recall — FDA D-0135-2020
Presence of Foreign Tablets/Capsules: Estradiol 1 mg was found in a 100 count bottle of Estradiol 0.5 mg Tablets.
Class IIFDA: TerminatedEpic Pharma, LLC
DrugOct 16, 2019
Sodium Chloride Injection USP 0.9% recall — FDA D-0138-2020
Labeling: Not Elsewhere Classified: RFID formatting error which reads product in Ultraject syringe as expired and will not allow injection of product by the Optivantage injector.
Class IIIFDA: TerminatedGUERBET LLC
DrugOct 16, 2019
GCP Laboratories Major Infants' Gas Relief Drops, Simethicone Oral Suspension USP, 1 FL OZ recall — FDA D-0126-2020
Microbial Contamination of Non-Sterile Product.
Class IIFDA: TerminatedGCP Laboratories Inc.
DrugOct 16, 2019
Unipharma, LLC DrKids Himasal Natural Nasal Saline Solution recall — FDA D-0133-2020
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Class IIFDA: TerminatedUnipharma, LLC.
DrugOct 16, 2019
LMD IN DEXTROSE 10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection, USP, 500 recall — FDA D-0136-2020
Lack of Assurance of Sterility: Bag has the potential to leak.
Class IIFDA: TerminatedPfizer Inc.
VehicleOct 16, 2019
Volkswagen Group of body recall — NHTSA campaign 19V737000
Volkswagen Group of America, Inc. (Audi) is recalling certain 2018-2019 Audi SQ5 and 2018-2020 Audi Q5 vehicles. The rear wheel arch cover trim may loosen and detach from the vehicle.
bodyVolkswagen Group of America, Inc.
VehicleOct 16, 2019
BMW pinion shaft recall — NHTSA campaign 19V738000
BMW of North America, LLC (BMW) is recalling certain 2020 BMW X3 M40i and X4 M40i vehicles. The steering rack pinion teeth may break under load, resulting in a loss of steering control.
pinion shaftBMW of North America, LLC
VehicleOct 10, 2019
Tesla Model 3 labels recall — NHTSA campaign 19V719000
Tesla Motors, Inc. (Tesla) is recalling certain 2019 Tesla Model 3 vehicles. The driver-side sun visor may not have the required air bag warning information. As such, these vehicles fail to…
labelsTesla, Inc.
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F, AR2.0, 100CM.070", REF SA6AR20. recall — FDA Z-2571-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
Medical DeviceOct 9, 2019
Medtronic Vascular SHERPA NX ACTIVE GUIDING CATHETER, 6F, RCB SH, 90CM, 070", REF SA6RCBSHD. recall — FDA Z-2605-2019
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Class IFDA: CompletedMedtronic Vascular
About the 2019 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.