The Recall Desk

Archive

December 2021 recalls

446 recalls were announced in December 2021.

What the numbers show

Critical
7
Severe
90
High
262
Moderate
74
Low
13

Of the 446 recalls this month scored against our rubric, 2% are Critical, 20% are Severe.

201–300 of 446

  • HighNHTSA·21V985000·2021-12-16

    Chevrolet and GMC Trucks: Spare Tire Incompatibility Disables Braking System

    General Motors is recalling certain 2019-2021 Chevrolet Silverado 1500 and GMC Sierra 1500 trucks. The supplied 17-inch spare tire is incompatible with aftermarket wheels, disabling the anti-lock braking system and increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V982000·2021-12-16

    2021 Ford Bronco Radar Misalignment Affects Cruise Control and Emergency Braking

    Ford is recalling certain 2021 Bronco and Ranger vehicles due to a misaligned cruise control radar module that may prevent the adaptive cruise control and emergency braking systems from functioning properly, increasing crash risk.

    Product
    FORD — FORD RANGER, BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V983000·2021-12-16

    Ford Recalls 2018 F-150 Trucks for Tailgate Latch Defect

    Ford is recalling 2018 F-150 trucks because tailgate latches may open unexpectedly while driving, creating a road hazard.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22713·2021-12-16

    Karmas Far Infant Bath Seats Recalled for Drowning Hazard

    Karmas Far infant bath seats fail federal safety standards and can tip over during use, posing a drowning hazard to babies. About 900 units sold online between August 2017 and October 2021 are affected. No injuries have been reported.

    Product
    Infant Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0344-2022·2021-12-15

    Puritan Bennett 980 Series Ventilators Recalled for Incorrect Capacitor Assembly

    Covidien is recalling 278 Puritan Bennett 980 Series Ventilators worldwide due to incorrect capacitor assembly that may cause devices to become inoperable during patient use.

    Product
    Puritan Bennett 980 Series Ventilator, 980U3ESDIUU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0335-2022·2021-12-15

    OsteoMed Surgical Consoles Recalled for Electrical Safety Violations

    OsteoMed OsteoPower Power Consoles and footswitches are being recalled due to non-compliance with electrical safety standard IEC 60601. The product has shocked a patient, creating a significant electrical hazard.

    Product
    OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 REF 450-0021-00 -OsteoMed D-Power Control Console 2 REF 450-0021-01 -Power Control Console 2 REF ECOS-450-0021-00 -OsteoMed OsteoPower Power Console 2i REF 450-0005-00 -OsteoMed D-Power Control Conso
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V971000·2021-12-15

    MCI Recalls Diesel Buses Due to Fuel Tube Fire Risk

    Motor Coach Industries is recalling 1,125 diesel buses because fuel tubes may crack and leak, increasing the risk of fire.

    Product
    MCI — MCI D45CRTLE, D4520, D4500, D4505
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0352-2022·2021-12-15

    Puritan Bennett 980 Series Ventilator Recall - Capacitor Assembly Error

    Covidien is recalling 278 Puritan Bennett 980 Series ventilators (model 980X3ENDIUU) due to a capacitor assembly error that may cause the device to become inoperable during patient use.

    Product
    Puritan Bennett 980 Series Ventilator, 980X3ENDIUU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0348-2022·2021-12-15

    Puritan Bennett 980 Ventilator recalled for capacitor assembly defect

    The Puritan Bennett 980 Series Ventilator may become inoperable due to a manufacturing defect in the internal capacitor assembly. A total of 278 units worldwide have been affected.

    Product
    Puritan Bennett 980 Series Ventilator, 980X1ENNISB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0339-2022·2021-12-15

    Puritan Bennett 980 Series Ventilator Recalled for Assembly Defect

    Covidien is recalling Puritan Bennett 980 Series Ventilators due to an assembly error in a capacitor. The defect may cause the ventilator to become inoperable during use.

    Product
    Puritan Bennett 980 Series Ventilator, 980A3ENNISB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0347-2022·2021-12-15

    Puritan Bennett 980 Series Ventilator Recalled for Manufacturing Assembly Defect

    Covidien LLC is recalling 278 units of the Puritan Bennett 980 Series Ventilator due to a manufacturing defect that may cause the device to become inoperable during clinical use.

    Product
    Puritan Bennett 980 Series Ventilator, 980X1ENDIUU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0266-2022·2021-12-15

    AmericanScreening Hand Sanitizer Recalled for Misleading Bottle Resemblance

    AmericanScreening Hand Sanitizer (ethyl alcohol 70%), 8 FL OZ bottles, is being recalled nationwide because the containers resemble drinking water bottles, posing a risk of accidental ingestion.

    Product
    AmericanScreening HAND SANITIZER (ethyl alcohol 70%) ANTIMICROBIAL FORMULA Vitamin E & Moisturizer, 8 FL OZ (237 mL) bottle with either a black or clear top, Distributed by American Screening LLC Shreveport, LA, 71106 UPC 8 40050 51579 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0341-2022·2021-12-15

    Puritan Bennett 980 Series Ventilator Recall Due to Manufacturing Defect

    Covidien is recalling 278 Puritan Bennett 980 Series Ventilators due to a manufacturing error where a capacitor was assembled incorrectly, which may cause the device to become inoperable during use.

    Product
    Puritan Bennett 980 Series Ventilator, 980S3ENDICU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0268-2022·2021-12-15

    TaDah! Falafel Street Wrap recalled for undeclared milk allergen

    The Fillo Factory Inc. is recalling TaDah! Falafel Street Wrap with Spicy Brown Sugar Harissa Hummus (7.5 oz) due to undeclared milk allergen. The product was distributed to retailers across multiple states.

    Product
    TaDah! FALAFEL STREET WRAP WITH SPICY BROWN SUGAR HARISSA HUMMUS NET WT. 7.5 OZ. UPC Code:8-5019800307-5
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Devices)·Z-0342-2022·2021-12-15

    Puritan Bennett 980 Ventilator Recalled for Capacitor Assembly Error

    Puritan Bennett 980 Series Ventilators are recalled due to an assembly error in a capacitor that may cause the device to become inoperable during use. The recall affects 278 units.

    Product
    Puritan Bennett 980 Series Ventilator, 980U1ENASAA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0269-2022·2021-12-15

    ELLENOS Mango Real Greek Yogurt Recall for Undeclared Egg Allergen

    ELLENOS Real Greek Yogurt in Mango flavor is recalled because the product contains egg but the label does not declare it. The recall affects 3,912 units distributed in Oregon and Washington.

    Product
    Mango Real Greek Yogurt, 16 oz., refrigerated item and packaged in a clear plastic container with a blue foil seal and can be identified by the blue lettering on front panel display. UPC on 16 oz. CUP is 8 57290 00612 6. The Mango Real Greek Yogurt label is read in parts: "*
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0346-2022·2021-12-15

    Puritan Bennett 980 Series Ventilator Recalled for Capacitor Assembly Defect

    Covidien is recalling 278 Puritan Bennett 980 Series Ventilators (Model 980X1ENDIPC) due to incorrect capacitor assembly that may cause the device to malfunction during use.

    Product
    Puritan Bennett 980 Series Ventilator, 980X1ENDIPC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0343-2022·2021-12-15

    Puritan Bennett 980 Ventilator Recalled for Capacitor Assembly Error

    Covidien is recalling the Puritan Bennett 980 Series Ventilator due to incorrect capacitor assembly that may cause the device to become inoperable during patient use.

    Product
    Puritan Bennett 980 Series Ventilator, 980U1ESDIUC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0245-2022·2021-12-15

    North Coast Smoked Salmon Trim Recalled for Listeria Contamination

    Oregon Lox Company is recalling North Coast Smoked Salmon Trim (3 lb packages, UPC 008603002551) due to potential Listeria monocytogenes contamination. The product was distributed in Alaska, California, Oregon, and Washington.

    Product
    North Coast Smoked Salmon Trim - Partial Slices of Cold Smoked Salmon, net wt. 3 lb. UPC 008603002551. The Ingredients statement on the label are read in parts: "***INGREDIENTS: Salmon, salt, brown sugar, sodium nitrite, FD&C Yellow 6/Red 40, natural hardwood smoke ***CONTAINS:
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0244-2022·2021-12-15

    North Coast Traditional Nova Lox Recall for Listeria monocytogenes

    Oregon Lox Company is recalling North Coast Traditional Nova Lox (cold smoked salmon) due to potential Listeria monocytogenes contamination. The product was distributed in Alaska, California, Oregon, and Washington.

    Product
    North Coast Traditional Nova Lox, cold smoked salmon, various net wt. 2-3lb average per side. UPC 008603005200. The Ingredients statement on the label are read in parts: "***INGREDIENTS: Wild Pacific salmon, corn oil, salt, brown sugar, sodium nitrite, FD&C Yellow 6/Red 40, natu
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0243-2022·2021-12-15

    Aqua Nova and Tony's Smoke House Smoked Salmon Recalled for Listeria

    Oregon Lox Company is recalling Aqua Nova and Tony's Smoke House smoked salmon products due to potential Listeria monocytogenes contamination. The recall affects products distributed in Alaska, California, Oregon, and Washington.

    Product
    Aqua Nova - Sliced Nova Lox, Oregon Cold Smoked Salmon, net wt. 3 oz. UPC 008603001608. Aqua Nova -Sliced Nova Lox, Oregon Cold Smoked Salmon, net wt. 1 lb. UPC 008603001400. Aqua Nova - Premium Oregon Nova Lox (Sliced), cold smoked salmon, various net wt 2-3 lbs per side. UPC
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0351-2022·2021-12-15

    Puritan Bennett 980 Series Ventilator Recalled for Assembly Error Risk

    Covidien is recalling 278 Puritan Bennett 980 Series Ventilators due to an assembly error in a capacitor that may cause the device to become inoperable during use. This recall affects units worldwide and in the US.

    Product
    Puritan Bennett 980 Series Ventilator, 980X2ESDIEC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0340-2022·2021-12-15

    Puritan Bennett 980 Series Ventilator Recalled for Manufacturing Defect

    Covidien Llc is recalling 278 Puritan Bennett 980 Series Ventilators due to a manufacturing assembly error where a capacitor may have been installed incorrectly, potentially causing device inoperability during use.

    Product
    Puritan Bennett 980 Series Ventilator, 980S1ENDICU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0338-2022·2021-12-15

    Puritan Bennett 980 Series Ventilator recalled for capacitor assembly error

    The Puritan Bennett 980 Series Ventilator is being recalled because a capacitor may be assembled incorrectly, which could cause the ventilator to stop working during use.

    Product
    Puritan Bennett 980 Series Ventilator, 980A1ENNISB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0349-2022·2021-12-15

    Puritan Bennett 980 Series Ventilator recalled for assembly defect

    Puritan Bennett 980 Series Ventilators are recalled due to a capacitor assembly error that may cause the device to become inoperable during use. The recall affects 278 units distributed worldwide.

    Product
    Puritan Bennett 980 Series Ventilator, 980X1JADIJJ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0353-2022·2021-12-15

    Puritan Bennett 980 Series Ventilator Recall Due to Assembly Error

    Covidien LLC is recalling 278 Puritan Bennett 980 Series Ventilators due to a capacitor assembly error that may cause the device to become inoperable during use. Affected devices were distributed worldwide with specific serial numbers targeted.

    Product
    Puritan Bennett 980 Series Ventilator, 980X3JADIJJ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0350-2022·2021-12-15

    Puritan Bennett 980 Series Ventilator Recall Due to Assembly Defect

    Covidien is recalling 278 Puritan Bennett 980 Series Ventilators worldwide due to an assembly error where a capacitor was incorrectly installed, potentially causing the device to become inoperable during use.

    Product
    Puritan Bennett 980 Series Ventilator, 980X1PLDIPC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V975000·2021-12-15

    Bentley vehicles recalled for incorrect airbag deployment information in owner manuals

    Bentley is recalling certain 2021-2022 vehicles because the owner's manual incorrectly states the airbag will not deploy when the Passenger Airbag On symbol is illuminated. This could cause unsafe positioning during a crash.

    Product
    BENTLEY — BENTLEY CONTINENTAL GT, FLYING SPUR, BENTAYGA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0274-2022·2021-12-15

    Wilbur Dark Chocolate Malted Milk Balls Recalled for Undeclared Peanuts

    Cargill Cocoa & Chocolate is recalling Wilbur Dark Chocolate Triple Covered Malted Milk Balls due to undeclared peanuts in the product. Consumers with peanut allergies face a serious health risk.

    Product
    Wilbur Dark Chocolate Triple Covered Malted Milk Balls, 1-pound (lb.) bags, clear plastic bags lot #211007 MB and 210917 MB , Item Code 200171-16
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0279-2022·2021-12-15

    Renata Plant-Based Suprema Pizza recalled for undeclared soy allergen

    Mi Piace LLC is recalling Renata Plant-Based Suprema Pizza because it contains undeclared soy allergen, which is not listed on the product label.

    Product
    Renata Plant-Based Suprema Pizza, frozen & vacuum packaged in plastic bags. Net wt: 420 gr (14.8 oz); UPC: 6 53467 38864 0; Manufactured by Renata Restaurant, 626 SE Main St, Portland, OR 97214; Product label, "Contains Wheat, Milk, Nuts, Coconut"
    Category
    Food
    Distribution
    2 states
  • HighCPSC·22032·2021-12-15

    Hisun 250cc Utility Vehicles Recalled for Fire Hazard

    Hisun Motors is recalling about 2,500 Sector 250cc and RK Performance 250cc utility vehicles sold at Rural King stores nationwide from November 2014 through June 2021 because grass can accumulate near the exhaust pipe and pose a fire hazard. The company has received five reports of vehicle fires but no injuries.

    Product
    Hisun 250cc Utility Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0354-2022·2021-12-15

    SuperCore Biopsy Instruments Recalled for Component Detachment Risk

    Argon Medical Devices is recalling 79,910 SuperCore Biopsy Instruments due to housing and plunger components detaching from the semi-automatic devices. The devices were distributed worldwide and throughout the United States.

    Product
    SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE BIOPSY INSTR 14GA X 9CM; 701114150/SUPERCORE BIOPSY INSTR 14GA X 15CM; 701116090/SUPERCORE BIOPSY INSTR 16GA X 9CM; 701118060/SUPERCORE BIOPSY INSTR 18GA X 6CM; 701118090/SUPERCORE BIOPSY INSTR 18GA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0281-2022·2021-12-15

    Spice House Sichuan Chile BBQ Rub Recall for Undeclared Sesame

    Spice House is recalling 737 units of its Sichuan Chile BBQ Rub because the product contains undeclared sesame, which is a major food allergen not listed on the label.

    Product
    The Spice House Sichuan Chile BBQ Rub 2.7oz glass jar UPC 816328028240
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0345-2022·2021-12-15

    Puritan Bennett 980 Ventilators Recalled Due to Manufacturing Assembly Error

    Covidien is recalling Puritan Bennett 980 Series Ventilators (model 980X1ENAIQC) due to an incorrectly assembled capacitor that may cause the device to become inoperable. The recall involves 278 units distributed worldwide, including the US.

    Product
    Puritan Bennett 980 Series Ventilator,980X1ENAIQC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0277-2022·2021-12-15

    Minute Maid Strawberry Lemonade Recalled for Possible Metal Contamination

    The Coca Cola Company is recalling Minute Maid Strawberry Lemonade (59 fl oz bottles) because they may contain a metal bolt or washer. The affected product has date code Jan0322 NP and Batch 0010259346.

    Product
    Minute Maid Strawberry Lemonade, 59 Fl. oz.(1.8 Qt) 1.75L, Unit UPC: 025000019708, Case UPC: 025000019760
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-0270-2022·2021-12-15

    Birds Eye Broccoli Tots Recalled for Small Rocks and Metal Fragments

    Conagra Brands is recalling Birds Eye Broccoli Tots (12 oz bags) due to the presence of small rocks and metal fragments in the product. Consumers should not eat the product and should dispose of it or return it.

    Product
    Birds Eye Broccoli Tots, frozen, 12OZ bag UPC 00-0-14500-00125-2
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0272-2022·2021-12-15

    Mountain Meadow Herbs Candida Flush capsules recalled for pressurization hazard

    Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3 capsules are being recalled because bottles may become pressurized over time, causing the cap, capsules, and product to be forcefully expelled when opened, risking hand and eye injury.

    Product
    Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, 240 capsules per bottle. UPC 8 13086 01593 2. This product is sold as part of our Total Yeast Detox Package or it can be purchased separately.
    Category
    Consumer Product
    Distribution
    12 states
  • HighFDA (Food)·F-0273-2022·2021-12-15

    H-E-B Creamy Tomato Basil Soup Recalled for Glass Contamination

    Fischer & Wieser Specialty Foods is recalling H-E-B Creamy Tomato Basil Soup due to potential glass contamination. The product was distributed in Texas.

    Product
    H-E-B Creamy Tomato Basil Soup NET WT 32 oz. packaged in a clear glass jar UPC 4122070619
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0278-2022·2021-12-15

    Minute Maid Fruit Punch recalled for potential metal foreign objects

    The Coca Cola Company is recalling Minute Maid Fruit Punch 59 fl. oz. bottles because they may contain metal foreign objects, including bolts or washers.

    Product
    Minute Maid Fruit Punch, 59 fl. oz.(1.8 QT)1.75 L, Unit UPC: 025000047725, Case UPC: 025000047732
    Category
    Food
    Distribution
    8 states
  • HighCPSC·22030·2021-12-15

    Schwinn Tone Electric Scooters recalled for fall and injury hazards

    Pacific Cycle is recalling about 11,340 Schwinn Tone electric scooters because the handlebar grips can loosen or crack, causing falls and injuries. One consumer fell and sustained bruising and abrasions when the handlebar broke during use.

    Product
    Schwinn Tone Electric Scooters (e-scooters)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0276-2022·2021-12-15

    Minute Maid Berry Punch recalled for possible metal object contamination

    The Coca Cola Company is recalling Minute Maid Berry Punch 59 fl. oz. bottles because they may contain a metal bolt or washer. Affected products were distributed in eight states.

    Product
    Minute Maid Berry Punch, 59 Fl. oz. (1.8 QT) 1.75 L, Unit UPC: 025000047664; Case UPC: 025000047671
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-0247-2022·2021-12-15

    Trader Joe's Organic Blue Corn Tortilla Chips recalled for undeclared milk

    Trader Joe's Organic Blue Corn Tortilla Chips (16 oz. bags) are being recalled due to undeclared milk allergen from co-mingling with butter popcorn during production.

    Product
    Trader Joe's Organic Blue Corn Tortilla Chips: 16 oz. bag, 15 bags per case
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·F-0246-2022·2021-12-15

    Whole Foods Cookies and Cream Cake Recalled for Undeclared Milk and Egg

    Whole Foods Market is recalling Cookies and Cream Single Layer Cake due to undeclared milk and egg allergens. The product was distributed in Colorado and may pose a risk to consumers with allergies.

    Product
    Whole Foods Market Cookies and Cream Single Layer Cake 8 inch NET WT 3lb 0 oz. (1361g) PLU: 39544 packaged in a clear plastic dome
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0355-2022·2021-12-15

    Philips BV Endura diagnostic X-ray system missing temperature specifications

    Philips BV Endura diagnostic X-ray systems lack specifications for maximum surface temperatures in their instructions, creating potential for burn injuries.

    Product
    BV Endura with Software Release 2.3- A mobile, diagnostic X-ray image acquisition and viewing system. Model Number: 718075
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0356-2022·2021-12-15

    Philips BV Pulsera X-ray Systems Missing Required Temperature Documentation

    Philips has recalled BV Pulsera mobile X-ray systems due to missing temperature specifications in the instructions for use. The X-ray tank and image intensifier lack maximum surface temperature documentation, creating a burn hazard.

    Product
    BV Pulsera with Software Release 2.3-A mobile, diagnostic X-ray image acquisition and viewing system. Model Number: 718095
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0332-2022·2021-12-15

    Covidien Sonicision Battery Charger Recalled Due to Electric Shock Risk

    Covidien is recalling Sonicision Battery Chargers (serial numbers MCSB006939 and MCSB006947) due to a risk of electric shock if used with a faulty or bypassed grounding circuit.

    Product
    Covidien Sonicision Battery Charger-intended to charge the Sonicision Reusable Battery Pack and to provide information on the battery charging progress and battery pack status Item Code: CBCA
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0357-2022·2021-12-15

    Diagnostic X-ray imaging system recalled for incomplete temperature specifications

    Philips Veradius Unity diagnostic X-ray systems lack required temperature specifications in instructions, creating burn risk. Affected systems should not be used until updated documentation is received.

    Product
    Veradius Unity with Software Release 2.1- Amobile, diagnostic X-ray imaging and viewing system. . Model Number: 718132
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0333-2022·2021-12-15

    Boston Scientific AUTOLITH TOUCH lithotripter power controls reversed in four languages

    Boston Scientific AUTOLITH TOUCH Bipolar Electrohydraulic Lithotripter devices distributed to Massachusetts have reversed high and low power settings in Russian, Romanian, Slovak, and Czech language versions. Users selecting a power level may receive the opposite setting.

    Product
    Boston Scientific AUTOLITH TOUCH Bipolar Electrohydraulic Lithotripter, REF M005466800. The device is designed to be used with Northgate Technologies Inc. bipolar disposable EHL probes for the fragmentation of calculi.
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·21V972000·2021-12-15

    Daimler Recalls 2019-2020 Sprinter Vehicles Due to Park Lock Software Error

    Daimler Vans USA is recalling 2019-2020 Mercedes-Benz and Freightliner Sprinter vans because a software error may allow the vehicle to move while in Park.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500, SPRINTER 1500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0267-2022·2021-12-15

    Allergy and Congestion tablets recalled due to failed dissolution specifications

    Dr. Reddy's Laboratories is recalling Allergy and Congestion (Fexofenadine HCl 60 mg & Pseudoephedrine HCl 120 mg) Extended-Release Tablets because they failed to meet dissolution specifications. Approximately 4,896 cartons distributed nationwide are affected.

    Product
    ALLERGY AND CONGESTION — ALLERGY AND CONGESTION (FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0271-2022·2021-12-15

    Gerber Macaroni and Cheese Recalled for Beetles in Peas

    Gerber is recalling Macaroni and Cheese with peas and carrots due to beetles found in the pea ingredient in the side compartment. The affected product has a best-by date of 04 Oct 2022.

    Product
    GERBER Macaroni and Cheese with a side of peas and carrots, 6.6 oz. (187 g) drained weight 5.3 oz. (150 g), 8 units per case.
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Drugs)·D-0271-2022·2021-12-15

    Antihistamine and Decongestant Tablets Recalled for Failed Dissolution

    Dr. Reddy's Laboratories is recalling Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg extended-release tablets distributed by Rugby Laboratories due to failed dissolution specifications. Affected lot AC2103329D (Exp 1/2023) was distributed nationwide in 2,184 cartons.

    Product
    Antihistamine & Nasal Decongestant, Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg, Extended Release Tablets USP, Allergy & Congestion, 12 Hour, 30 Tablets, Distributed by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152, www.rugbylaboratories.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0269-2022·2021-12-15

    OTC Allergy and Congestion Tablets Recalled for Failed Dissolution

    Dr. Reddy's Laboratories is recalling 5,016 cartons of Fexofenadine HCl 60 mg / Pseudoephedrine HCl 120 mg Extended Release Tablets nationwide due to failed dissolution specifications. Affected lot is AC2103329F with expiration 1/2023.

    Product
    FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI — FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI (FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0270-2022·2021-12-15

    Fexofenadine and Pseudoephedrine Tablets Recalled for Failed Dissolution

    Dr. Reddy's Laboratories is recalling Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg Extended Release Tablets because they failed dissolution specifications, which may affect how the medication works in the body.

    Product
    Antihistamine & Nasal Decongestant, Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg, Extended Release Tablets USP, Allergy & Congestion, 12 Hour, 20 Tablets, Distributed by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152, www.rugbylaboratories.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0274-2022·2021-12-15

    Walmart Allergy Relief D Extended-Release Tablets Recalled for Failed Dissolution

    Dr. Reddy's Laboratories is recalling Walmart brand Allergy Relief D extended-release tablets (Lot #AC2103329B) nationwide because the tablets failed to meet dissolution specifications, which may affect medication effectiveness.

    Product
    Allergy Relief D Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg, Extended Release Tablets, USP, 30 Extended-Release Tablets USP, Distributed By Walmart Inc., Bentonville, AR 72716, Product of India, NDC 49035-273-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0277-2022·2021-12-15

    Apollo Care VANComycin Injection Recalled for Crystallization

    Apollo Care is recalling VANComycin 1g in 0.9% Sodium Chloride injection due to crystallization that makes the product appear turbid. The affected lot was distributed in Missouri.

    Product
    VANComycin 1g added to 250mL of 0.9% Sodium Chloride (Injection for Intravenous Use Only), 260 mL per bag, Rx Only, This is a Compounded Drug, Hospital/Office Use Only, Apollo Care 3801 Mojave Ct, Suite 101, Columbia, MO 65202, NDC 71170-254-25
    Category
    Drug
    Distribution
    1 state
  • ModerateCPSC·22033·2021-12-15

    Ceiling Fans Recalled Due to Detaching Blades Impact Injury Risk

    About 77,900 Harbor Breeze Belleisle Bay and Honeywell Rio ceiling fans are recalled because the blades can detach during use and strike consumers or cause property damage.

    Product
    Harbor Breeze Belleisle Bay and Honeywell Rio Ceiling Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0334-2022·2021-12-15

    Orthodontic Software Documentation Recalled for Unapproved Labeling Changes

    Orchestrate Orthodontic Technologies recalls O3D ORCHESTRATE user documentation because the labeling was altered from its FDA-approved version. Approximately 127 copies were distributed to practitioners worldwide.

    Product
    O3D ORCHESTRATE Orthodontic Technologies User Manual and Data Processing Instructions (model preparation for tooth movement) MKT-LB-002 Rev 1 for Orchestrate3d Software v.3.1 - v5.0.4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0276-2022·2021-12-15

    Hydrocodone Bitartrate and Acetaminophen tablets recalled for product mix-up

    Ascent Pharmaceuticals is recalling Hydrocodone Bitartrate and Acetaminophen 10 mg/325 mg tablets nationwide due to a product mix-up. The recall affects 9,744 bottles and was voluntarily initiated by the manufacturer.

    Product
    HYDROCODONE BITARTRATE AND ACETAMINOPHEN — HYDROCODONE BITARTRATE AND ACETAMINOPHEN (HYDROCODONE BITARTRATE AND ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0275-2022·2021-12-15

    Fexofenadine and Pseudoephedrine Tablets Recalled for Failed Dissolution

    Dr. Reddy's Laboratories is recalling Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg extended-release tablets because they failed to meet dissolution specifications, which may affect how the medication works in the body.

    Product
    FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI — FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI (FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0268-2022·2021-12-15

    CVS Allergy & Congestion Relief Tablets Recalled for Failed Dissolution

    Dr. Reddy's Laboratories is recalling CVS Allergy & Congestion Relief tablets (fexofenadine HCl 60 mg/pseudoephedrine HCl 120 mg extended-release) nationwide due to failed dissolution specifications.

    Product
    Allergy & Congestion Relief Allergy Relief D, Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Extended Release Tablets, 20 extended-release tablets, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, Made in India, NDC 69842-249-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0272-2022·2021-12-15

    Fexofenadine and Pseudoephedrine allergy relief tablets recalled for failed dissolution

    Dr. Reddy's Laboratories is recalling a 12 HR Allergy & Congestion Relief product distributed nationwide because the tablets failed to meet dissolution specifications, which may affect drug effectiveness.

    Product
    12 HR Allergy & Congestion Relief Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg Antihistamine I Nasal Decongestant, 20 Extended-Release Tablets USP, Distributed By Cardinal Health, Dublin, Ohio 43107, Made in India, NDC 70000-0518-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0273-2022·2021-12-15

    CVS Allergy Relief D Extended-Release Tablets Recall

    CVS Allergy Relief D extended-release tablets (Fexofenadine HCl 60 mg / Pseudoephedrine HCl 120 mg) are being recalled because they failed dissolution specifications, meaning the tablets may not release the medication properly.

    Product
    Allergy Relief D Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg, Extended Release Tablets, 30 Extended-Release Tablets USP, Distributed By CVS Pharmacy Inc., One CVS Drive, Woonsocket, RI 02985, Made in India, NDC 69842-249-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·047-2021·2021-12-14

    Margherita Pepperoni Recalled for Possible Bacillus Cereus Contamination

    Smithfield Packaged Meats is recalling approximately 10,990 pounds of Margherita pepperoni due to possible Bacillus cereus contamination. No illnesses have been reported.

    Product
    Smithfield Packaged Meats Corp. Dba Margherita Meats Inc. Recalls Pepperoni Products Due to Possible Bacillus Cereus Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V969000·2021-12-14

    Spartan K3 RV Chassis Models Recalled for Fuel System Defect

    Shyft Group is recalling 2020-2023 Spartan K3 RV chassis vehicles because fuel tubes may fatigue and crack, creating a potential fuel leak and fire risk. Dealers will install vibration isolators or replace fuel tubes at no cost.

    Product
    SPARTAN — SPARTAN K3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V961000·2021-12-13

    Mercedes-Benz Recalls Vehicles Due to Fuel Leak Fire Risk

    Mercedes-Benz is recalling specific gasoline-engine vehicles because trapped particles may cause a fuel leak, increasing the risk of a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 300, GLA 250, AMG GT63, SL 550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V962000·2021-12-13

    Sutphen Recalls 2016-2020 Fire Trucks Due to Fuel Leak Risk

    Sutphen is recalling 2016-2020 fire trucks because fuel tubes may crack, causing high-pressure leaks that increase fire risk.

    Product
    SUTPHEN — SUTPHEN FIRE TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V966000·2021-12-13

    Autocar Xpeditor GPS Module Mounting Defect May Interfere With Brakes

    Autocar is recalling certain 2021-2022 Xpeditor vehicles because the GPS module may be improperly mounted and could come loose, potentially interfering with brake and throttle pedals.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V965000·2021-12-13

    Western Star and Freightliner Trucks Fuel Tubes May Crack, Fire Risk

    Fuel tubes in certain 2019–2022 Western Star, Freightliner, and FCCC trucks may crack, causing high-pressure fuel leaks that could ignite. DTNA is offering free replacement of fuel tubes and installation of vibration isolators.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER, FCCC 4700, 114SD, 49X, 47X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V963000·2021-12-13

    2022 Toyota 4Runner recalled for inoperable high beam after fog light installation

    Southeast Toyota Distributors is recalling certain 2022 Toyota 4Runner vehicles because the driver's side high beam may become inoperable after installation of accessory fog lights. This reduces visibility and increases crash risk.

    Product
    TOYOTA — TOYOTA 4RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V964000·2021-12-13

    Seagrave Fire Trucks Recalled for Fuel Tube Cracking and Fire Risk

    Seagrave is recalling 2019-2021 fire trucks with Cummins X12 engines because fuel tubes may crack, causing high-pressure leaks and fire risks.

    Product
    SEAGRAVE — SEAGRAVE CAPITAL, ATTACKER, MARAUDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V960000·2021-12-10

    KME Predator Fire Risk Recall Due to Fuel Tube Cracking

    KME is recalling 2020-2022 Predator and Severe Service vehicles because fuel tubes may crack, causing high-pressure leaks that increase fire risk.

    Product
    KME — KME PREDATOR SS, PREDATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22029·2021-12-10

    Target Recalls Decorative Mailbox Due to Laceration Hazard

    Target is recalling approximately 174,300 Letters to Santa Mailboxes because the mail slot can be sharp, posing a laceration hazard. Target has received seven reports of lacerations, three of which required medical attention.

    Product
    Letters to Santa Mailbox
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V953000·2021-12-09

    Mack Trucks Recalls TerraPro Models Due to Parking Brake Release Risk

    Mack Trucks is recalling certain TerraPro vehicles because a brake control valve air leak can cause the parking brake to release unexpectedly, increasing the risk of a crash.

    Product
    MACK — MACK TERRAPRO (MRU), TE, MRU, TERRAPRO (TE)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V952000·2021-12-09

    E-One Recalls Fire Trucks Due to Fuel Tube Cracking Risk

    E-One is recalling specific 2019-2021 Quest II, Typhoon, and Cyclone models because fuel tubes may crack, causing high-pressure leaks and fire risks.

    Product
    E-ONE — E-ONE QUEST II, TYPHOON, CYCLONE II, CYCLONE N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V954000·2021-12-09

    Subaru Recalls 2020 Ascent Vehicles for Steering Tie Rod Defect

    Subaru is recalling 2020 Ascent vehicles because front tie rod ends may not fit properly, potentially causing loss of steering control and increasing crash risk.

    Product
    SUBARU — SUBARU ASCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V949000·2021-12-09

    2021 Jeep Wrangler 4XE Recalled for Odometer Display Failure

    Chrysler is recalling 2021 Jeep Wrangler 4XE vehicles because the odometer stops displaying mileage after 13,342 miles, potentially delaying critical safety maintenance.

    Product
    JEEP — JEEP WRANGLER 4XE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V950000·2021-12-09

    2021 Jeep Grand Cherokee L Inoperable Headlight Software Defect Recall

    Certain 2021 Jeep Grand Cherokee L vehicles may have inoperable headlights due to a smart lighting module software defect. This reduces visibility and increases the risk of crashes.

    Product
    JEEP — JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V956000·2021-12-09

    Autocar Xpeditor and Legend fuel tubes may crack, risking fire

    Autocar is recalling 2019-2022 Xpeditor and 2020-2022 Legend vehicles. Fuel tubes may crack, causing a high-pressure leak that could ignite in the presence of a fire source.

    Product
    AUTOCAR — AUTOCAR XPEDITOR, LEGEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V951000·2021-12-09

    Prevost Recalls 2020-2022 X3 Buses Due to Loose Ceiling Panel

    Prevost is recalling 2020-2022 X3 Commuter and X3 Coach buses because the front ceiling panel may fall, posing a crash or injury risk.

    Product
    PREVOST — PREVOST X3 COM, X3 COACH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V957000·2021-12-09

    2021 Nissan Rogue recalled for fuel pump failure and engine stall risk

    Nissan is recalling approximately 24,793 2021 Rogue vehicles due to abnormal wear in the fuel pump that may cause overheating, failure, and engine stall, increasing crash risk.

    Product
    NISSAN — NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V958000·2021-12-09

    2022 Nissan Frontier left-rear seat belt bracket bolts loose

    Certain 2022 Nissan Frontier vehicles have seat belt bracket mounting bolts on the left-rear seat that may have been incorrectly tightened. In a crash, a loose bracket may break, causing loss of seat belt restraint and increased injury risk.

    Product
    NISSAN — NISSAN FRONTIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0226-2022·2021-12-08

    Alsum Farms Yellow Onions Recalled for Salmonella Risk

    Alsum Farms & Produce is recalling whole yellow onions in 3 lb. and 5 lb. bags due to potential Salmonella contamination. Consumers should not eat the affected product.

    Product
    Alsum Farms & Produce Whole Yellow Onions packaged in 3 lbs. (1.36kg) UPC 39186-60002 and 5 lbs. (2.27kg) UPC 39186-60003 bags. Produce of Mexico. Packed by Alsum Farms & Product, Inc., Friesland, WI 53935.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0261-2022·2021-12-08

    Biotin Solution for Injection recalled due to lack of sterility assurance

    ASP CARES is recalling Biotin Solution for Injection (10 mg/mL, 30 mL vials) because the manufacturer cannot assure the product's sterility. The affected lot was distributed in the United States.

    Product
    Biotin Solution for Injection, 10 mg/mL, 30 mL Multiple Dose Vial, Sterile, For IM or IV use only, Rx only ASP Cares, 2414 Babcock Rd Ste #106, San Antonio, TX 78229 NDC 72833-0589-30
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Food)·F-0227-2022·2021-12-08

    Alsum Farms Red Onions Recalled Due to Salmonella Risk

    Alsum Farms & Produce is recalling whole red onions in 2-pound bags due to potential Salmonella contamination. Affected bags have specific lot codes and were distributed in Illinois, Michigan, Pennsylvania, and Wisconsin.

    Product
    Alsum Farms & Produce Whole Red onions packaged in 2lb. (907g) bags, UPC 39186-60101 Produce of Mexico. Packed by Alsum Farms & Product, Inc., Friesland, WI 53935.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0286-2022·2021-12-08

    Sandoz Enoxaparin Sodium Injection Recalled Due to Temperature Excursion

    Sandoz Inc. is recalling 45,036 cartons of Enoxaparin Sodium Injection USP 40 mg/0.4 mL due to temperature abuse during shipping. The affected lot was distributed nationwide.

    Product
    Enoxaparin Sodium Injection, USP, 40 mg/0.4 mL, Single-Dose Syringes with Automatic Safety Device, For Subcutaneous Injection, Rx Only; 0.4 mL Syringes, Manufactured for Sandoz Inc., Princeton, NJ 08540, NDC 00781-3246-02; Carton (10 x 0.4 mL Syringes), Manufactured by Shenzhen T
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0220-2022·2021-12-08

    Natural Delight Collection Dried Apricots Recalled for Undeclared Sulfites

    ILG International Trading, Inc. is recalling Natural Delight Collection Natural Dried Apricots due to the presence of undeclared sulfites, which poses a health risk to sensitive consumers.

    Product
    Natural Delight Collection Natural Dried Apricots, product of Uzbekistan; in a 500 g (17 oz) cardboard box marked with a best before date of 03/30/2022. The product UPC code is 811579000533
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·21V945000·2021-12-08

    2022 Thomas Built SAF-T-LINER C2 School Buses: Gas Pedal Misalignment Risk

    Daimler Trucks North America is recalling 2022 Thomas Built SAF-T-LINER C2 school buses because the gas pedal assembly may be misaligned and wear through the floor mat, potentially trapping the pedal and causing unintended acceleration.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0225-2022·2021-12-08

    Alsum Farms Whole White Onions Recalled for Salmonella Risk

    Alsum Farms & Produce is recalling Whole White Onions, 2 lbs. bags (UPC 39186-60051, Lot 169008) due to potential Salmonella contamination. The onions were distributed in Illinois, Michigan, Pennsylvania, and Wisconsin.

    Product
    Alsum Farms & Produce Whole White Onions, 2 lbs. (907g) UPC 39186-60051. Produce of Mexico. Packed by Alsum Farms & Product, Inc., Friesland, WI 53935.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0231-2022·2021-12-08

    WEL-PAC Powdered Shrimp Stock Recall: Undeclared Fish Allergen

    WEL-PAC Brand Shrimp Dashi No Moto powdered shrimp stock is being recalled because the label fails to declare fish (hydrolyzed protein containing bonito, sardine, and tuna). The product contains undeclared fish allergen.

    Product
    WEL-PAC Brand Shrimp Dashi No Moto - Powdered Shrimp Stock; Net Wt. 1.75 oz. (0.35.oz x 5 bags) 49.6 g UPC: 0 11152 83660 7 Product of Japan; Imported by JFC International Inc., Los Angeles, CA 90040 INGREDIENTS: SALT, MONOSODIUM GLUTAMATE, SUGAR, GLUCOSE, SHRIMP EXT
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0262-2022·2021-12-08

    Ascorbic Acid Injection Recalled Due to Lack of Sterility Assurance

    ASP CARES is recalling Ascorbic Acid Solution for Injection (500 mg/mL, 50 mL vials) distributed in the United States because the manufacturer cannot assure the product meets sterility requirements.

    Product
    Ascorbic Acid Solution for Injection, 500 mg/mL, 50 mL Multiple Dose Vial, For IM, IV or SC Use Only, Rx only, ASP Cares, 2414 Babcock Rd Ste #106, San Antonio, TX 78229 NDC 72833-690-50
    Category
    Drug
    Distribution
    0 states
  • SevereNHTSA·21V946000·2021-12-08

    Western Star 4900 Recalled for Steering Shaft Pinch Bolt Issue

    Daimler Trucks North America is recalling 2021-2022 Western Star 4900 vehicles because the steering shaft pinch bolt may not be properly tightened, risking loss of steering control.

    Product
    WESTERN STAR — WESTERN STAR 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V947000·2021-12-08

    Audi SQ5 and Q5 recalled for water ingress into control module

    Volkswagen Group of America (Audi) is recalling certain 2018–2022 Audi Q5 and SQ5 vehicles. Water or liquid can seep into the gateway control module, causing sudden engine power loss and increasing crash risk.

    Product
    AUDI — AUDI Q5, SQ5, Q5 SPORTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide

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