FoodAug 10, 2022
The Procter & Gamble Company Vicks ZzzQuil Liquid Melatonin Syrup Adult 8oz plastic bottle recall — FDA F-1537-2022
Acidified/Low Acid dietary supplement with no approved process.
Class IIFDA: TerminatedThe Procter & Gamble Company
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 61
Records are ordered by the best available source date.
FoodAug 10, 2022
United Natural Foods MEAT AND POULTRY PRODUCTS 1 recall — FDA F-1527-2022
Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.
Class IIFDA: TerminatedUnited Natural Foods, Inc.
FoodAug 10, 2022
United Natural Foods REFRIDGERATED VEGETABLE PRODUCTS 1 recall — FDA F-1523-2022
Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.
Class IIFDA: TerminatedUnited Natural Foods, Inc.
FoodAug 10, 2022
United Natural Foods refrigerated BEVERAGE 1 recall — FDA F-1517-2022
Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.
Class IIFDA: TerminatedUnited Natural Foods, Inc.
FoodAug 10, 2022
Vitamin Cottage Natural Food Markets Amaranth Grain Organic, brand Natural Grocers, packaged recall — FDA F-1511-2022
Potential to be contaminated with Salmonella
Class IIFDA: TerminatedVitamin Cottage Natural Food Markets, Inc.
FoodAug 10, 2022
United Natural Foods REFRIDGERATED DIPS 1 recall — FDA F-1519-2022
Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.
Class IIFDA: TerminatedUnited Natural Foods, Inc.
FoodAug 10, 2022
United Natural Foods FROZEN PREPARED FOODS 1 recall — FDA F-1524-2022
Two food trailers holding various types and brands of frozen foods were temperature abused during deliver to two retail stores.
Class IIFDA: TerminatedUnited Natural Foods, Inc.
FoodAug 10, 2022
The Procter & Gamble Company Vicks Children's Botanicals Liquid Nighttime 4oz plastic recall — FDA F-1535-2022
Acidified/Low Acid dietary supplement with no approved process.
Class IIFDA: TerminatedThe Procter & Gamble Company
DrugAug 10, 2022
Ultra Supplement SUSTANGO recall — FDA D-1350-2022
Marketed Without an Approved NDA/ANDA: Analytical testing showed the presence of tadalafil.
Class IFDA: TerminatedUltra Supplement LLC
DrugAug 10, 2022
Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 180 mg, 30-count bottle recall — FDA D-1302-2022
Failed Dissolution Specifications: below specification limits for dissolution.
Class IIFDA: TerminatedTeva Pharmaceuticals USA Inc.
DrugAug 10, 2022
Distributor RFR, LLC SANGTER Energy Supplement Capsules, 3000mg x 7 grain, 7-count blister recall — FDA D-1333-2022
Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil.
Class IFDA: TerminatedDistributor RFR, LLC.
DrugAug 10, 2022
Teva Pharmaceuticals USA Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 240 recall — FDA D-1303-2022
Failed Dissolution Specifications: below specification limits for dissolution.
Class IIFDA: TerminatedTeva Pharmaceuticals USA Inc.
DrugAug 10, 2022
Tacrolimus Ointment, 0.1%, For Dermatological Use Only, Not for Ophthalmic Use recall — FDA D-1304-2022
Defective Container: Tube split from side seam
Class IIIFDA: OngoingGlenmark Pharmaceuticals Inc., USA
DrugAug 10, 2022
Tolmar Naftifine Hydrochloride Gel, USP 1% recall — FDA D-1300-2022
Failed Impurities/ degradation specifications: Out-of-Specification test results obtained for Unspecified Impurity Relative Retention Time
Class IIFDA: TerminatedTolmar, Inc.
VehicleAug 8, 2022
Maverick curtain recall — NHTSA campaign 22V594000
Ford Motor Company (Ford) is recalling certain 2022 Maverick vehicles. The side-curtain air bags may not deploy properly. As such, these vehicles fail to comply with the requirements of…
curtainFord Motor Company
Medical DeviceAug 3, 2022
Integra LifeSciences CereLink ICP Monitor recall — FDA Z-1395-2022
Integra has received complaints associated with ICP readings drifting to -50 mmHg (out-of-range) and may manifest an error message "sensor or extension cable failure!" The firm has found…
Class IFDA: OngoingIntegra LifeSciences Corp.
Medical DeviceAug 3, 2022
Meridian Bioscience Revogene, Catalog no. 610210 recall — FDA Z-1479-2022
When a run is aborted, the cooling period protection does not occur and the user is able to open the lid prior to the completion of the cooling period, exposing the user to heated…
Class IIFDA: OngoingMeridian Bioscience Inc.
Medical DeviceAug 3, 2022
Covidien TruClear Hysteroscopic Tissue Removal System Control Unit- designed to meet the recall — FDA Z-1467-2022
Electrical component failure within the control unit. The observed failure mode is a loss of function of the device when used with handpiece and foot switch.
Class IIFDA: OngoingCovidien LLC
Medical DeviceAug 3, 2022
Bard Access Systems Intraosseous needle and driver recall — FDA Z-1397-2022
BD Intraosseous Needle Kits may exhibit: 1) Increased force required to remove the stylet from intraosseous needle during placement may cause removal of the entire needle assembly and loss…
Class IFDA: OngoingBard Access Systems, Inc.
Medical DeviceAug 3, 2022
Intuitive Surgical Da Vinci X/Xi Large Clip Applier, Model 470230 Da Vinci X/Xi Medium-Large recall — FDA Z-1460-2022
Due to the potential for unexpected motion caused by the partial disengagement of the instrument from the system.
Class IIFDA: OngoingIntuitive Surgical, Inc.
Medical DeviceAug 3, 2022
NuVasive Description/Part: Simplify Disc Size 1, Ht 5/SM-5 recall — FDA Z-1453-2022
Cervical artificial disc Unique Device Identifier (UDI) barcodes contain the incorrect Global Trade Item Number (GTIN) on the Patient Label when scanned and may also contain the incorrect…
Class IIFDA: OngoingNuVasive Inc.
Medical DeviceAug 3, 2022
Medline Convenience kits labeled as: a recall — FDA Z-1474-2022
Kits contain leaking bottles of isopropyl alcohol
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - SPT
Medical DeviceAug 3, 2022
Baxter Healthcare ABACUS TPN recall — FDA Z-1376-2022
There is a potential risk of medication error when using specific Abacus Order Entry & Calculation software.
Class IFDA: TerminatedBaxter Healthcare Corporation
Medical DeviceAug 3, 2022
Stryker 2.3mm Tapered Router, Catalog no. 5820-071-023 instrument used in craniotomy recall — FDA Z-1478-2022
There is a potential for the core diameter to be undersized, which may lead to the router breaking. A break can lead to unintended metal fragments in the surgical site, resulting in the…
Class IIFDA: OngoingStryker Instruments
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.