FoodFeb 19, 2020
Ready Pac Bistro - Spinach Dijon Salad with Sweet Onion Dijon recall — FDA F-0740-2020
Incorrect ingredient label was put on salad product and does not declare eggs and wheat.
Class IIFDA: TerminatedReady Pac Foods, Inc.
Latest records
Latest recalls — page 1080
The newest recall records with useful source details are listed here.
FoodFeb 19, 2020
WORLDWIDE SEAFOOD PRODUCTS 103200 - TIDAL SEAFOOD YELLOWFIN TUNA 10 lb, 2x10 lb cases and recall — FDA F-0679-2020
Product is being recalled due to potentially elevated levels of histamines.
Class IIFDA: TerminatedWORLDWIDE SEAFOOD PRODUCTS LLC
FoodFeb 19, 2020
MORTON SALT;THIS SALT DOES NOT SUPPLY IODIDE recall — FDA F-0682-2020
Canisters containing Iodized Salt are labeled with Plain Salt labels, causing dextrose and potassium iodide to be undeclared ingredients.
Class IIIFDA: TerminatedMorton Salt Inc.
FoodFeb 19, 2020
Meijer Fresh From Meijer diced hard boiled eggs sold by weight from recall — FDA F-0683-2020
Possible L. mono contamination in hard boiled eggs
Class IFDA: TerminatedMeijer
DrugFeb 19, 2020
GSK Consumer Health Theraflu Cough Relief, Dextromethorphan HBr and Guaifensin, 6 packets recall — FDA D-0996-2020
Labeling: Label Lacks Warning: Product recalled due to absence of a warning statement on the product label, Ask a doctor before use if you have a sodium-restricted diet.
Class IIFDA: TerminatedGSK Consumer Health, Inc.
DrugFeb 19, 2020
RemedyRepack Ketorolac Trom, 30 mg/1mL Inj. for I.V./I.M recall — FDA D-0867-2020
Presence of Particulate Matter: Medication relabeled at facility was recalled by the manufacturer due to small black particles noticed during routine visual inspection. of retain samples.
Class IFDA: TerminatedRemedyRepack Inc.
DrugFeb 19, 2020
Raloxifene Hydrochloride Tablets, USP, 60 mg, 30 Tablets (3 x 10 blister cards) recall — FDA D-0854-2020
Failed Dissolution Specifications: Low out of specification results obtained during stability testing.
Class IIFDA: TerminatedAmerican Health Packaging
DrugFeb 19, 2020
Caduet recall — FDA D-0842-2020
Defective Container: products potentially could have been packaged in defective bottles, with a notched rim, that could cause inadequate foil sealing resulting in lack of moisture…
Class IIFDA: TerminatedPfizer Inc.
DrugFeb 19, 2020
Caduet recall — FDA D-0841-2020
Defective Container: products potentially could have been packaged in defective bottles, with a notched rim, that could cause inadequate foil sealing resulting in lack of moisture…
Class IIFDA: TerminatedPfizer Inc.
DrugFeb 19, 2020
Pfizer Fentanyl Citrate Inj., USP 100 mcg Fentanyl/2 mL (50 mcg/mL), 2 mL Single-dose Vial recall — FDA D-0835-2020
Defective Container: confirmed customer reports for vials with loose metal overseal crimp defects, which may result in lack of assurance of sterility.
Class IIFDA: TerminatedPfizer Inc.
DrugFeb 19, 2020
Akorn Hydrocortisone and Acetic Acid Otic Solution, USP, 10 mL dropper bottle recall — FDA D-0839-2020
Subpotent Drug: Low Out of specification (OOS) assay results for the hydrocortisone portion of this product.
Class IIFDA: TerminatedAkorn Inc.
DrugFeb 19, 2020
Par Pharmaceutical Frovatriptan Succinate Tablets, 2.5mg recall — FDA D-0843-2020
Labeling: Incorrect or Missing Lot and/or Exp Date: Product incorrectly labeled with an expiration date of August 2022 rather than the correct expiration date of April 2022.
Class IIIFDA: TerminatedPar Pharmaceutical Inc.
DrugFeb 19, 2020
Contract Pharmacal Leader Extra Strength Acetaminophen Tablets, 500 mg Pain Reliever/Fever recall — FDA D-0857-2020
Presence of Foreign Tablets/Capsules: Complaint involving one Women's Prenatal dietary supplement tablet commingled in a bottle of Extra Strength Acetaminophen 500 mg contents 1000 count…
Class IIFDA: TerminatedContract Pharmacal Corporation
DrugFeb 19, 2020
Amoxicillin and Clavulanate Potassium Tablets, USP, 875 mg/125 mg, 20-count bottles recall — FDA D-0852-2020
Presence of Foreign Substance: Customer complaint of a foreign substance identified as nylon cable tie
Class IIFDA: TerminatedAuroMedics Pharma LLC
DrugFeb 19, 2020
Memantine Hydrochloride Extended Release Capsules, 21 mg, 30-count bottles recall — FDA D-0855-2020
Failed Dissolution Specifications: Low out of specification results observed in dissolution test at six-month long-term stability study.
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugFeb 19, 2020
Lamotrigine Tablets, USP, 100 mg recall — FDA D-0833-2020
Cross Contamination; Lamotrigine Tablets 100 mg USP was contaminated with enalapril maleate.
Class IFDA: TerminatedTaro Pharmaceuticals U.S.A., Inc.
DrugFeb 19, 2020
ACETAMINOPHEN Major Extra Strength Acetaminophen Tablets, 500 mg Pain Reliever/Fever Reducer recall — FDA D-0858-2020
Presence of Foreign Tablets/Capsules: Complaint involving one Women's Prenatal dietary supplement tablet commingled in a bottle of Extra Strength Acetaminophen 500 mg contents 1000 count…
Class IIFDA: TerminatedContract Pharmacal Corporation
VehicleFeb 19, 2020
Audi Q7 side/window recall — NHTSA campaign 20V093000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2019 Audi Q7 vehicles. In the event of a crash, the side curtain air bags may not properly inflate.
side/windowVolkswagen Group of America, Inc.
VehicleFeb 13, 2020
Chrysler transfer case (4-wheel drive) recall — NHTSA campaign 20V080000
Chrysler (FCA US LLC) is recalling certain 2019 Ram 1500 pickup trucks equipped with four-wheel drive. A gear within the transfer case may not have been installed correctly, possibly…
transfer case (4-wheel drive)Chrysler (FCA US LLC)
Medical DeviceFeb 12, 2020
Datascope Reinforced Introducer Sets Maquet 7.5 Fr., Part Number: 068400040305 recall — FDA Z-0933-2020
Potential for compromised sterility in breached pouches of specific lots of Reinforced Introducer Sets Maquet 7 Fr., 7.5 Fr. and 8 Fr. IABs.
Class IIFDA: TerminatedDatascope Corporation
Medical DeviceFeb 12, 2020
Cardinal Health AAMI 3 FABREINF SURG GOWN LARGE, Item Code 9511 recall — FDA Z-1040-2020
The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
Class IIFDA: TerminatedCardinal Health
Medical DeviceFeb 12, 2020
Cardinal Health AAMI 3 FABRNF SCRUB SURG GWN XL NS, Gown recall — FDA Z-1006-2020
The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
Class IIFDA: TerminatedCardinal Health
Medical DeviceFeb 12, 2020
Cook Fixed Core Straight Safety Wire Guide, Guidewire, Global Product Number G14285 recall — FDA Z-0960-2020
The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip.
Class IIFDA: TerminatedCook Inc.
Medical DeviceFeb 12, 2020
Cardinal Health AAMI 3 ROYALSILK SURGGOWN BNS 2XL, Item Code 9578NB recall — FDA Z-1013-2020
The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
Class IIFDA: TerminatedCardinal Health
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
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