FoodAug 17, 2022
Big Olaf Creamery LLC dba Big Olaf Frozen Ice Cream to include all flavors, sold in sizes recall — FDA F-1542-2022
Products may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedBig Olaf Creamery LLC dba Big Olaf
Monthly breakdown
2022 recalls by month
Select a month to review the recall records reported during that period.
December 2022318 records · 4 categoriesNovember 2022270 records · 4 categoriesOctober 2022288 records · 4 categoriesSeptember 2022318 records · 4 categoriesAugust 2022293 records · 4 categoriesJuly 2022334 records · 4 categoriesJune 2022348 records · 4 categoriesMay 2022227 records · 4 categoriesApril 2022205 records · 4 categoriesMarch 2022449 records · 4 categoriesFebruary 2022237 records · 4 categoriesJanuary 2022296 records · 4 categories
2022 recalls — page 59
Records are ordered by the best available source date.
FoodAug 17, 2022
NATURE'S SUNSHINE PRODUCTS Aivia Whey Protein+ Power Herbs Vanilla Bean, NET WT recall — FDA F-1541-2022
Label declares Whey but does not declare Milk.
Class IIFDA: TerminatedNATURE'S SUNSHINE PRODUCTS
FoodAug 17, 2022
BrandStorm Natierra Nature & Earth Organic Blueberries Ingredients recall — FDA F-1539-2022
Elevated levels of lead detected as a result of testing conducted by Maryland Department of Health.
Class IIFDA: TerminatedBrandStorm Inc.
DrugAug 17, 2022
Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/12.5 mg, 30 Tablets recall — FDA D-1306-2022
Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .
Class IIFDA: TerminatedGlenmark Pharmaceuticals Inc., USA
DrugAug 17, 2022
SYSTANE LUBRICANT Systane, Lubricant Eye Drops, Polyethylene Glycol 400 0.4% Lubricant recall — FDA D-1314-2022
CGMP Deviations: products were stored outside the drug label specifications.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
DrugAug 17, 2022
Lorazepam Injection, USP, 2mg/mL, 1 mL vial, 25 vials per carton recall — FDA D-1307-2022
Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.
Class IIFDA: TerminatedHikma Pharmaceuticals USA Inc.
DrugAug 17, 2022
Naphcon A eye drops, Naphazoline HCl 0.025% and Pheniramine Maleate 0.3%, Redness Reliever recall — FDA D-1313-2022
CGMP Deviations: products were stored outside the drug label specifications.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
DrugAug 17, 2022
Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/25 mg, 30 Tablets recall — FDA D-1305-2022
Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .
Class IIFDA: TerminatedGlenmark Pharmaceuticals Inc., USA
DrugAug 17, 2022
Prednisone Tablets USP, 20 mg, 100-count bottle recall — FDA D-1330-2022
Presence of foreign tablet: 2.5 mg tablet in a 20 mg bottle of Prednisone Tablets
Class IIFDA: TerminatedStrides Pharma Inc.
DrugAug 17, 2022
Lorazepam Injection, USP, 4mg/mL, 1 mL vial, 25 vial per carton recall — FDA D-1310-2022
Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.
Class IIFDA: TerminatedHikma Pharmaceuticals USA Inc.
DrugAug 17, 2022
Mckesson Medical-Surgical Inc. Corporate Office Triple Antibiotic Ointment, Bacitracin zinc recall — FDA D-1311-2022
CGMP Deviations: products were stored outside the drug label specifications.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
DrugAug 17, 2022
DAKINS QUARTER Dakin's Solution, a) sodium hypochlorite 0.125%, quarter strength, NDC recall — FDA D-1323-2022
CGMP Deviations: products were stored outside the drug label specifications.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
DrugAug 17, 2022
Lorazepam Injection, USP, 2mg/mL, 1 mL vial, 25 vial per carton recall — FDA D-1309-2022
Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.
Class IIFDA: TerminatedHikma Pharmaceuticals USA Inc.
DrugAug 17, 2022
Mckesson Medical-Surgical Inc. Corporate Office Asthmanefrin Racephinephrine Inhalation recall — FDA D-1324-2022
CGMP Deviations: products were stored outside the drug label specifications.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
DrugAug 17, 2022
S2 Racepinephrine Inhalation Solution, USP 2.25%, Bronchodilator, For Oral Inhalation Only recall — FDA D-1325-2022
CGMP Deviations: products were stored outside the drug label specifications.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
DrugAug 17, 2022
Ativan Injection (lorazepam injection, USP), 2mg/mL, 1 mL vial, 25 vials per carton recall — FDA D-1308-2022
Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.
Class IIFDA: TerminatedHikma Pharmaceuticals USA Inc.
DrugAug 17, 2022
PATADAY ONCE DAILY RELIEF Pataday, Once Daily Relief, Olopatadine hydrochloride ophthalmic recall — FDA D-1321-2022
CGMP Deviations: products were stored outside the drug label specifications.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
DrugAug 17, 2022
ZADITOR Systane Zaditor, ketotifen fumarate ophthalmic solution 0.035%, Antihistamine eye recall — FDA D-1317-2022
CGMP Deviations: products were stored outside the drug label specifications.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
VehicleAug 15, 2022
Telluride trailer hitch recall — NHTSA campaign 22V626000
Kia America, Inc. (Kia) is recalling certain 2020-2022 Telluride vehicles potentially equipped with a Genuine Kia 4-pin tow hitch harness installed as original equipment, or purchased as an…
trailer hitchKia America, Inc.
VehicleAug 15, 2022
Palisade motor recall — NHTSA campaign 22V627000
Hyundai Motor America (Hyundai) is recalling certain 2020-2021 Palisade vehicles. The windshield wiper motor may become inoperative, causing the wipers to fail.
motorHyundai Motor America
VehicleAug 12, 2022
F-150 driveshaft recall — NHTSA campaign 22V623000
Ford Motor Company (Ford) is recalling certain 2021-2022 F-150 vehicles. Underbody heat and noise insulators may loosen and contact the aluminum driveshaft, which could damage the…
driveshaftFord Motor Company
VehicleAug 12, 2022
Impreza headlights recall — NHTSA campaign 22V624000
Subaru of America, Inc. (Subaru) is recalling certain 2017-2019 Impreza vehicles. The left and right side reflex reflector and left side low beam reflector may inadequately reflect light.…
headlightsSubaru of America, Inc.
VehicleAug 11, 2022
General Motors critical fasteners recall — NHTSA campaign 22V617000
General Motors, LLC (M) is recalling certain 2021-2022 Cadillac Escalade, Escalade ESV, Chevrolet Suburban, Tahoe, GMC Yukon, and Yukon XL vehicles equipped with third-row seats. The rivet…
critical fastenersGeneral Motors, LLC
Medical DeviceAug 10, 2022
Medtronic Medline Sprinter OTW, Model/Catalog Number SPR2512W recall — FDA Z-1483-2022
Luer has balloon diameter printed as "2.25mmx12mm" instead of the correct diameter, "2.5mmx12mm" as reflected on the product outer packaging.
Class IIFDA: OngoingMedtronic Inc.
About the 2022 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.