The Recall Desk

Archive

June 2021 recalls

771 recalls were announced in June 2021.

What the numbers show

Critical
10
Severe
119
High
371
Moderate
260
Low
11

Of the 771 recalls this month scored against our rubric, 1% are Critical, 15% are Severe.

501–600 of 771

  • HighNHTSA·21V427000·2021-06-04

    Keystone Recalls 2019-2020 RVs Due to Propane Regulator Fire Risk

    Keystone is recalling 2019 Bullet and Sprinter and 2020 Hideout RVs because a propane regulator may fail, increasing fire risk.

    Product
    KEYSTONE — KEYSTONE HIDEOUT, BULLET, SPRINTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V428000·2021-06-04

    Recreational vehicles recalled for propane regulator failure and fire risk

    Heartland and Cruiser recreational vehicles with defective Winntec propane regulators may experience increased pressure, enlarging gas-appliance flames and increasing fire risk. Dealers will replace the regulator free of charge.

    Product
    HEARTLAND — HEARTLAND, CRUISER RV, CRUISER SUNDANCE, TRAIL RUNNER, LITHIUM, PROWLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·21147·2021-06-03

    Fisher-Price Recalls Rock 'n Glide Soothers After Four Infant Deaths

    Fisher-Price is recalling 4-in-1 Rock 'n Glide Soothers and 2-in-1 Soothe 'n Play Gliders due to reports of four infant deaths from suffocation.

    Product
    Fisher-Price 4-in-1 Rock 'n Glide Soothers and 2-in-1 Soothe 'n Play Gliders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V422000·2021-06-03

    2021 GMC Acadia Fuel Supply Line Recall Due to Fire Risk

    General Motors is recalling certain 2021 GMC Acadia vehicles due to improperly attached fuel supply lines. The lines may loosen or separate, causing fuel leaks and increasing the risk of fire.

    Product
    CADILLAC — CADILLAC, GMC XT5, XT6, ACADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V424000·2021-06-03

    Land Rover Defender Recall for Engine Stall Risk

    Land Rover is recalling 2020-2021 Defender vehicles with 6-cylinder engines because the powertrain control module may unexpectedly switch off, causing an engine stall.

    Product
    LAND ROVER — LAND ROVER DEFENDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V420000·2021-06-03

    Sea-Doo Move I Extended 1500 Trailer Recalled for Wheel Spindle Weld Defect

    Bombardier is recalling 2021 Sea-Doo Move I Extended 1500 trailers because improperly welded wheel spindles can break, causing the wheel to detach and increasing crash risk.

    Product
    SEA-DOO — SEA-DOO MOVE I EXTENDED 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V423000·2021-06-03

    GM Recalls 2019 Silverado and Sierra 1500 for Tire Sidewall Defect

    General Motors is recalling 2019 Chevrolet Silverado 1500 and GMC Sierra 1500 vehicles because over-cured tires may develop sidewall breaks, risking sudden air loss and loss of vehicle control.

    Product
    GMC — GMC, CHEVROLET SIERRA 1500, SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21752·2021-06-03

    Kalorik Recalls Electric Steakhouse Grills Due to Electric Shock Hazard

    Kalorik is recalling Pro 1500F Electric Steakhouse Grills because incorrectly electroplated knobs can cause electric shocks after the grill preheats.

    Product
    Kalorik Pro 1500F Electric Steakhouse Grills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0396-2021·2021-06-02

    Acella Recalls Subpotent NP Thyroid 15 Prescription Tablets

    Acella Pharmaceuticals is recalling NP Thyroid 15 tablets because they contain less active ingredient than labeled. The recall covers specific lots distributed nationwide.

    Product
    NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0397-2021·2021-06-02

    Acella Recalls Subpotent NP Thyroid 15 Tablets Nationwide

    Acella Pharmaceuticals is recalling 154,726 bottles of NP Thyroid 15 tablets because they contain less active ingredient than labeled.

    Product
    NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0395-2021·2021-06-02

    Acella Recalls Subpotent NP Thyroid 15 Tablets Nationwide

    Acella Pharmaceuticals is recalling NP Thyroid 15 tablets because they contain less active ingredient than labeled. The recall covers bottles distributed nationwide.

    Product
    NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0625-2021·2021-06-02

    Safeway Fresh Foods Recalls Robinson Fresh Turnip Greens Due to Listeria

    Safeway Fresh Foods is voluntarily recalling Robinson Fresh Turnip Greens because the product tested positive for Listeria monocytogenes.

    Product
    Robinson Fresh, Turnip Greens, 1lb. packages / Bags, 8 packages per case , Perishable/Keep Refrigerated . BEST IF USED BY 04/26/21 .
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1625-2021·2021-06-02

    Philips Respironics BiPAP V30 Auto Recall for Non-Conforming Plastic Material

    Philips Respironics is recalling 22 BiPAP V30 Auto ventilators because non-conforming plastic in motor assemblies may cause toxic off-gassing or sudden device failure.

    Product
    BiPAP V30 Auto, US market: Continuous ventilator, non-life-supporting. Material Number: 1111178
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1628-2021·2021-06-02

    Philips Respironics BiPAP A40 System Silver Recalled for Motor Assembly Defect

    Philips Respironics is recalling four BiPAP A40 System Silver units due to non-conforming plastic in motor assemblies that may off-gas or fail, posing asphyxia risks.

    Product
    BiPAP A40 System Silver, JP: Continuous ventilator, non-life-supporting. Material Number: 1111177
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0624-2021·2021-06-02

    American Pop Corn Recalls Buttered Microwave Popcorn for Undeclared Milk Allergen

    American Pop Corn Co. is recalling buttered microwave popcorn bags packaged in boxes that fail to declare the major food allergen milk.

    Product
    Xtra Butter Microwave Popcorn bags packaged in cardboard boxes labeled to be Jolly Time Healthy Pop 100's Kettle Corn 100 Calorie Singles, 3 1.2 oz (34 g) Net Wt 4.8 oz (136 g), American Pop Corn Co. Sioux City, Iowa
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Food)·F-0631-2021·2021-06-02

    Torn Ranch Organic Dark Chocolate Blueberries Recalled for Undeclared Almonds

    Torn Ranch LLC is recalling one lot of Organic Dark Chocolate Blueberries due to a potential undeclared allergen (tree nuts-almonds).

    Product
    Torn Ranch Organic Dark Chocolate Blueberries 18oz. resealable bags UPC: 036412020169 Item code: 2016-18-CW Produced by Torn Ranch Petaluma, CA 94954
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0567-2021·2021-06-02

    Indianapolis Fruit Company Recalls Organic Coleslaw Due to Plastic Foreign Material

    Indianapolis Fruit Company is recalling Garden Cut Coleslaw W/ Carrot Organic due to the presence of plastic foreign material. The product was distributed to retailers in six states.

    Product
    Garden Cut Coleslaw W/ Carrot Organic, 1lb plastic clamshell, UPC 053495081016, 4 1lb retail units per wholesale case. Item number: CACO41L / 17671
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1630-2021·2021-06-02

    Philips Respironics BiPAP A40 Ventilator Recall for Material Defects

    Philips Respironics is recalling four BiPAP A40 ventilators because non-conforming plastic in the motor assembly may cause toxic off-gassing or sudden device failure.

    Product
    BiPAP A40, Brazil: Continuous ventilator, non-life-supporting. Material Number: BR1111169
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1626-2021·2021-06-02

    Philips Respironics BiPAP A40 Ventilators Recalled for Motor Assembly Defects

    Philips Respironics is recalling 10 BiPAP A40 ventilators due to non-conforming plastic in motor assemblies that may cause toxic off-gassing or sudden device failure.

    Product
    BiPAP A40, China: Continuous ventilator, non-life-supporting. Material Number - CN1111169
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1627-2021·2021-06-02

    Philips BiPAP A40 System Silver Recalled for Motor Assembly Defects

    Philips Respironics is recalling specific BiPAP A40 System Silver units due to non-conforming plastic in motor assemblies that may cause off-gassing or sudden device failure.

    Product
    BiPAP A40 System Silver, JP: Continuous ventilator, non-life-supporting. Material Number: R1111177
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0632-2021·2021-06-02

    Sara Lee and Chef Pierre Pecan Pies Recalled for Undeclared Peanut

    Sara Lee Frozen Foods is recalling specific pecan pie products due to potentially undeclared peanut. Consumers should check labels and stop using the affected items.

    Product
    Sara Lee Pecan Pie 4oz. retail packaged UPC 032100051118, 24 and 48 count wholesale case; Chef Pierre Southern Pecan Pie, 10 slices, 36oz. retail packaged UPC 032100092739, 6 pies per wholesale case; Chef Pierre Pecan Pie, 10 slices, 36oz. retail packaged UPC 032100093750, 6…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0459-2021·2021-06-02

    Cardinal Health Recalls Synjardy Tablets Due to Temperature Excursions

    Cardinal Health is recalling 751 bottles of Synjardy XR tablets distributed in Florida, Georgia, and South Carolina due to intermittent temperature exposure during storage.

    Product
    SYNJARDY — SYNJARDY (EMPAGLIFLOZIN, METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1629-2021·2021-06-02

    Philips Respironics BiPAP A30 Ventilator Recall for Motor Assembly Defect

    Philips Respironics is recalling two BiPAP A30 ventilators due to non-conforming plastic in motor assemblies that may cause toxic off-gassing or sudden device failure.

    Product
    BiPAP A30, Brazil: Continuous ventilator, non-life-supporting. Material Number: BR1111143
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V414000·2021-06-02

    Volvo Recalls 2019-2020 Models for Fuel Pump Fuse Failure Risk

    Volvo is recalling 2019-2020 models because a fuel pump fuse can fail, causing the vehicle to stall and increasing crash risk.

    Product
    VOLVO — VOLVO V60CC, V90CC, V60, XC90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0399-2021·2021-06-02

    Acella Recalls Subpotent NP Thyroid 15 Tablets Nationwide

    Acella Pharmaceuticals is recalling NP Thyroid 15 tablets because they contain less active ingredient than labeled. The recall covers bottles distributed nationwide.

    Product
    NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V418000·2021-06-02

    Stonebrooke RAM 5500 Recalled for Rear Brake Fluid Leak Risk

    Stonebrooke is recalling one 2019 RAM 5500 because the rear brake line can wear and leak, increasing crash risk.

    Product
    STONEBROOKE EQUIPMENT — STONEBROOKE EQUIPMENT RAM 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0561-2021·2021-06-02

    Wild Rice Split Pea Soup Recalled for Undeclared Wheat and Soy

    The Secret Garden of Park Rapids is recalling Wild Rice Split Pea Soup because it contains undeclared wheat and soy allergens.

    Product
    Wild Rice Split Pea Soup, UPC 91675-71000, The Secret Garden, Park Rapids, MN 56470
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0626-2021·2021-06-02

    Brill Inc Recalls Chocolate Chip Cookies for Potential Foreign Objects

    Brill Inc is recalling specific batches of 12-inch chocolate chip message cookies due to a potential risk of containing small foreign objects.

    Product
    10194739 TranSmart" 12 INCH CHOCOLATE CHIP MESSAGE COOKIE 24/24 OUNCE CHOCOLATE CHIP COOKIES IN BAKEABLE PLASTIC PANS WITH DOMES KEEP FROZEN AT 0¿F OR BELOW Net weight: 36 lb (16.33 kg) (24 x 24 oz (680g))
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V415000·2021-06-02

    Genesis Supreme Wanderer and Vortex RV Trailers Recalled for Cooking Stove Gas Leak

    Genesis Supreme RV is recalling certain 2020-2021 Wanderer and Vortex trailers with Dometic cooking stoves. An overtightened saddle valve securing bolt can damage the seal and cause a gas leak, increasing fire risk.

    Product
    GENESIS SUPREME — GENESIS SUPREME VORTEX, WANDERER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E049000·2021-06-02

    Adventurer Truck Campers Recalled for Potential Gas Leak from Dometic Stoves

    Adventurer LP is recalling specific truck campers equipped with Dometic stoves because a saddle valve bolt may be overtightened, causing a gas leak that increases fire risk.

    Product
    EQUIPMENT:APPLIANCE:OVEN/STOVE/COOKTOP recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1683-2021·2021-06-02

    Radiometer Recalls PICO70 Arterial Blood Samplers Due to Sterile Barrier Breach

    Radiometer is recalling PICO70 Arterial Blood Samplers because a sterile barrier breach was found during testing, posing a risk of bacterial infection.

    Product
    PIC070 Arterial Blood Sampler PICO70 - Product Usage: Preheparinized, electrolyte-balanced, arterial blood sampler product line for collection of arterial samples for pH, blood gas, oximetry, electrolyte and metabolite analysis. Model Number/Product Description: 956-518…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1672-2021·2021-06-02

    Welch Allyn GS777 Wall Transformer Recalled for Electrical Shock Risk

    Welch Allyn is recalling GS777 Wall Transformers due to a potential risk of fluid ingress causing electrical shorts and shock.

    Product
    GS777 Wall Transformer Model: 77710 Intended Use: The GS777 Wall Transformer is intended for use in ambulatory and acute care settings.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V413000·2021-06-02

    2021 Volkswagen ID.4 recalled for incorrect headlight aiming caps

    Volkswagen is recalling certain 2021 ID.4 vehicles because headlight aiming caps were installed on the vertical adjustment instead of the horizontal adjustment. This defect can increase glare and reduce visibility, increasing the risk of a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0627-2021·2021-06-02

    Brill Inc Recalls Jumbo Chocolate Chip Cookies Due to Foreign Objects

    Brill Inc is recalling Jumbo Chocolate Chip Cookies nationwide because they may contain small foreign objects.

    Product
    10233579 JUMBO CHOCOLATE CHIP COOKIE 12 / 12 INCH BAKED CHOCOLATE CHIP COOKIES KEEP FROZEN Net weight: 17.04 lb (7.73 kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1670-2021·2021-06-02

    Beckman Coulter Access SARS-CoV-2 Antigen Recalled for False Negative Risk

    Beckman Coulter is recalling Access SARS-CoV-2 Antigen test kits because specimens stored in certain conditions may yield false negative results.

    Product
    Access SARS-CoV-2 Antigen, REF C68668, UDI: (01)15099590742713, 3.30 mL/R1a, 4.70 mL/R1b, 4.20 mL/R1c, 3.10 mL, R1d, 3.10 mL, R1e
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V416000·2021-06-02

    Mack 2021-2022 trucks recalled for hubcap separation hazard

    Mack Trucks is recalling 307 certain 2021-2022 Granite, Pinnacle, and Anthem commercial trucks due to a defective hubcap compression spring that can cause the hubcap to separate, creating a road hazard and increasing crash risk.

    Product
    MACK — MACK PINNACLE (CHU), GRANITE (GR), ANTHEM (AN), GRANITE (GU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V410000·2021-06-02

    Mercedes-Benz Sprinter Recall for Swivel Seat Wiring Harness Defect

    Daimler Vans USA is recalling 2019-2021 Mercedes-Benz and Freightliner Sprinter vans with swivel seats because incorrect wiring harness routing may damage the seat air bag system.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 4500, SPRINTER 3500, SPRINTER 1500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1682-2021·2021-06-02

    Pentax Medical Video Duodenoscope Recalled for Distal End Cap Detachment Risk

    Pentax of America Inc. is recalling 108 Pentax Medical Video Duodenoscopes because the distal end cap may detach during procedures, posing risks of injury or aspiration.

    Product
    Pentax Medical Video Duodenoscope - Product Usage: intended to be used with endoscopic devices and other ancillary equipment to provide optical visualization of (via a video monitor), and therapeutic access to, Biliary Tract via the Upper Gastrointestinal Tract, Model Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1673-2021·2021-06-02

    Welch Allyn ProBP 3400 Digital Blood Pressure Device Recall

    Welch Allyn is recalling ProBP 3400 Digital Blood Pressure Devices due to a risk of fluid ingress causing electrical shorts and potential shock.

    Product
    ProBP 3400 Digital Blood Pressure Device ((handheld, desk mount, wall mount models) Model: 34XFHT-B Intended: ProBP 3400 automatically measures systolic and diastolic pressure (excluding neonates) and pulse rate, as well as calculates Mean Arterial Pressure (MAP).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1684-2021·2021-06-02

    Baxter Gambro Cartridge Blood Set Recalled for Potential Leak Risk

    Baxter Healthcare is recalling Gambro Cartridge Blood Sets due to a potential leak between the venous patient connector and the patient's hemodialysis access.

    Product
    Gambro Cartridge Blood Set, Product Code 101025 - Product Usage: intended for single use in a hemodialysis treatment using the Phoenix Dialysis Delivery Systems.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1687-2021·2021-06-02

    James Leckey MyWay Walker Chassis Recalled Due to Weld Failure

    James Leckey Design Ltd is recalling 2,719 MyWay Walker Chassis units because weld failures caused casters to detach from the rear legs.

    Product
    MyWay Walker Chassis - Product Usage: is intended for use by children already using a supportive walking device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1676-2021·2021-06-02

    Dentech Corp. Recalls Rubber Dam Clamps Due to Possible Breakage

    Dentech Corp. is recalling 87,842 units of KSK Rubber Dam Clamps because they may break during use. The recall covers units distributed in the US and worldwide.

    Product
    Rubber Dam Clamp, KSK - Product Usage: used for prevention of contamination by saliva and moisture prevention during dental treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0629-2021·2021-06-02

    Croissant Etc. Recalls Frozen Croissant Crusts for Undeclared Soy Lecithin

    Croissant Etc. Corp. is recalling 20 cases of frozen 6-inch round croissant crusts because they contain undeclared soy lecithin.

    Product
    6" Round Croissant Crust 100 Count Bulk, frozen, Net Weight: 6.25 lbs. Croissant Etc. Corp., Greendale, WI 53129
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·21V411000·2021-06-02

    Mercedes-Benz and Freightliner Sprinter Recalled for Rearview Camera Software Defect

    Daimler Vans USA is recalling 2019-2021 Mercedes-Benz and Freightliner Sprinter vans because a software defect may cause the rearview camera image to fail to display.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 4500, SPRINTER 1500, SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1671-2021·2021-06-02

    Philips IntelliVue MX40 Patient Monitor Recalled for Manufacturing Defects

    Philips is recalling three IntelliVue MX40 patient monitors because manufacturing process failures may have resulted in defective devices.

    Product
    IntelliVue MX40 Patient Monitor, Model Number: 865350 (US) 865352 (OUS) Software version number B.06.59 - Product Usage: Intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults and pediatrics in hospital environments and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0560-2021·2021-06-02

    Wild Rice Tomato Soup Recalled for Undeclared Wheat and Soy Allergens

    The Secret Garden of Park Rapids is recalling Wild Rice Tomato Soup because it contains undeclared wheat and soy allergens.

    Product
    Wild Rice Tomato Soup, UPC 91675-31004, The Secret Garden, Park Rapids, MN 56470
    Category
    Food
    Distribution
    4 states
  • HighUSDA FSIS·PHA-06022021·2021-06-02

    USDA Issues Public Health Alert for Raw Breaded Stuffed Chicken Products

    USDA FSIS issued a public health alert for frozen raw breaded stuffed chicken products due to a Salmonella Enteritidis illness cluster. Consumers are advised to cook products to 165 F.

    Product
    FSIS Issues Public Health Alert for Frozen Raw Breaded Stuffed Chicken Products Due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V417000·2021-06-02

    Volvo Trucks recalls 2021-2022 vehicles for hubcap separation hazard

    Volvo Trucks is recalling certain 2021-2022 VAH, VDH, VNL, and VNR vehicles due to a defective hubcap compression spring that can cause the hubcap to separate, creating a road hazard. Dealers will remove the hubcap free of charge.

    Product
    VOLVO — VOLVO VNL, VAH, VHD, VNR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0522-2021·2021-06-02

    Cardinal Health Recalls Belsomra Tablets Due to Temperature Excursions

    Cardinal Health is recalling 119 cartons of Belsomra (suvorexant) 10 mg tablets due to intermittent temperature excursions during storage.

    Product
    Belsomra (suvorexant) tablets 10 mg Each tablet contains 10 mg suvorexant. This package contains 30 Tablets in 3 Blister Cards. Each Blister Card contains 10 Tablets Rx only NDC 00006-0033-30 Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. Whitehouse Station, NJ…
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0585-2021·2021-06-02

    Cardinal Health Recalls Folivane-Plus Capsules Due to Temperature Excursions

    Cardinal Health is recalling 80 bottles of Folivane-Plus capsules because they were intermittently exposed to temperature excursions during storage.

    Product
    Folivane-Plus with Ascorbic Acid Precursors Iron/Folic Acid/Vitamin Supplement Capsules 90 Capsules Rx Only NDC 13811-539-90 Manufactured for: Trigen Laboratories, Inc., Sayreville, NJ 08872
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0587-2021·2021-06-02

    Cardinal Health Recalls Restora Omega-3 Supplement Due to Temperature Excursions

    Cardinal Health Inc. is recalling 31 cartons of Restora Omega-3 enhanced Lactobacillus Casei KE-99 30 Capsules due to intermittent exposure to temperature excursions during storage.

    Product
    Restora Omega-3 enhanced Lactobacillus Casei KE-99 30 Capsules 1 A Day Nutritional Supplement NDC 52747-200-30 Marketed by US Pharmaceutical Corporation, P.O. Box 360465, Decatur, GA 30036
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1679-2021·2021-06-02

    Nobel Biocare Implant Crown Recalled for Manufacturing Specification Defects

    Nobel Biocare Procera LLC is recalling specific implant crown units because they were not manufactured to specification. The recall affects units distributed in the US and several international countries.

    Product
    NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s4 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw creating a prosthetic device (full contour crown), and to restore the patient s chewing function and esthetics. Material Number: 77363
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1675-2021·2021-06-02

    Roche Recalls Iron Gen 2 Reagent Cassettes Due to Discrepant Results

    Roche Diagnostics is recalling 20,468 Iron Gen 2 reagent cassettes because they may produce discrepant elevated results on specific analyzers.

    Product
    IRON GEN 2: ROCHE COBAS INTEGRA ANALYZER, REAGENT CASSETTES, Catalog#: 03183696122 - Product Usage: In vitro test for the quantitative determination of iron in human serum and plasma on Roche/Hitachi cobas c and cobas Integra systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0432-2021·2021-06-02

    Cardinal Health Recalls Gemcitabine Injection Due to Temperature Excursions

    Cardinal Health is recalling Gemcitabine Injection 200mg/5.26ml vials due to intermittent temperature excursions during storage. The product was distributed in Florida, Georgia, and South Carolina.

    Product
    GEMCITABINE INJECTION 200MG/5.26ML; NDC/UPC 72485-221-02; RX; SINGLEDOSE VIAL
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1681-2021·2021-06-02

    Nobel Biocare Procera LLC Recalls Implant Crowns Not Manufactured to Specification

    Nobel Biocare Procera LLC is recalling specific implant crowns because they were not manufactured to specification. The recall affects units distributed in the US and several international countries.

    Product
    NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s6 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw creating a prosthetic device (full contour crown), and to restore the patient s chewing function and esthetics. Material Number: 77387
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1674-2021·2021-06-02

    Siemens Centaur Syphilis Assay Recalled for Potential Carryover Interference

    Siemens Healthcare Diagnostics is recalling the Centaur Syphilis Assay-SYP Kit due to potential carryover into other assays on specific systems.

    Product
    Centaur Syphilis Assay-SYP Kit, 200 Test - Product Usage: For in vitro diagnostic use in the qualitative determination of antibodies to Treponema pallidum in human serum or plasma using the ADVIA Centaur XP/XPT System and ADVIA Centaur CP Systems, SMN:10492493
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0478-2021·2021-06-02

    Cardinal Health Recalls Advair HFA Inhalers Due to Temperature Excursions

    Cardinal Health is recalling 297 units of Advair HFA inhalers due to intermittent temperature exposure during storage. The product was distributed in Florida, Georgia, and South Carolina.

    Product
    ADVAIR HFA 45-21MCG 12GM; NDC/UPC 173071520; RX; INHALER MEDICAL INTERNAL - MAY OR MAY NOT BE AEROSOL
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0573-2021·2021-06-02

    Cardinal Health Recalls Proair HFA Inhalers Due to Temperature Excursions

    Cardinal Health Inc. is recalling 26,895 Proair HFA inhalers due to intermittent exposure to temperature excursions during storage.

    Product
    Proair HFA (albuterol sulfate) Inhalation Aerosol 90 mcg per actuation With Dose Counter 200 Metered Inhalation 8,5 g Net Contents Rx only NDC 59310-579-22 Mktd by: Teva Respiratory, LLC Horsham, PA 19044 Mfd by: IVAX Pharmaceuticals Ireland Waterford, Ireland
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0516-2021·2021-06-02

    Cardinal Health Recalls Vitamin D3 Tablets Due to Temperature Excursions

    Cardinal Health Inc. is recalling 19 bottles of Vitamin D3 25mcg tablets because they were intermittently exposed to temperature excursions during storage.

    Product
    VITAMIN D3 25MCG 180 TABLETS; NDC/UPC 880681168011; OTC; TABLETS
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0539-2021·2021-06-02

    Cardinal Health Recalls Zolpidem Tablets Due to Temperature Excursions

    Cardinal Health is recalling 55 boxes of Zolpidem Tartrate Sublingual Tablets 3.5 mg due to intermittent exposure to temperature excursions during storage.

    Product
    ZOLPIDEM TARTRATE SUBLINGUAL TABLET 3.5 MG 30 UNIT DOSE POUCHES; NDC/UPC 49884089911; RX; EACH POUCH CONTAINS ONE SUBLINGUAL TABLET
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0543-2021·2021-06-02

    Cardinal Health Recalls Benzoyl Peroxide Acne Wash Due to Temperature Excursions

    Cardinal Health is recalling 31 bottles of Benzoyl Peroxide 10% Acne Medication Wash due to intermittent temperature exposure during storage. The product was distributed in Florida, Georgia, and South Carolina.

    Product
    Benzoyl Peroxide 10% Acne Medication Wash Net Wt 5 oz (142 g) Distributed By Perrigo Allegan, MI 49010, NDC 45802-318-01
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0497-2021·2021-06-02

    Cardinal Health Recalls Tylenol Acetaminophen Liquid Gels Due to Temperature Excursions

    Cardinal Health Inc. is recalling 37 bottles of Tylenol Acetaminophen Liquid Gels because of intermittent temperature exposure during storage.

    Product
    Tylenol Acetaminophen Pain Regular Strength Liquid Gels Pain Reliever Fever Reducer 20 Liquid Gels 325 mg each NDC 50580-487-20
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0487-2021·2021-06-02

    Cardinal Health Recalls Hydrocortisone Ointment Due to Temperature Excursions

    Cardinal Health Inc. is recalling 23 tubes of Hydrocortisone Ointment USP 1% due to intermittent exposure to temperature excursions during storage.

    Product
    Hydrocortisone Ointment USP 1% Maximum Strength Net Wt. 1 oz (28 g) NDC 0472-0345-56 Manufactured by: Actavis Mid Atlantic LLC 1877 Kawai Road, Lincolnton, NC 28902
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0544-2021·2021-06-02

    Cardinal Health Recalls Polyethylene Glycol 3350 Powder for Temperature Excursions

    Cardinal Health Inc. is recalling 163 bottles of Polyethylene Glycol 3350 Powder for Solution due to intermittent exposure to temperature excursions during storage.

    Product
    POLYETHYLENE GLYCOL 3350 — POLYETHYLENE GLYCOL 3350 (POLYETHYLENE GLYCOL 3350)
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0416-2021·2021-06-02

    Cardinal Health Recalls Restasis Eye Drops Due to Temperature Excursions

    Cardinal Health Inc. is recalling 3,688 bottles of Restasis 0.05% eye drops due to intermittent exposure to temperature excursions during storage.

    Product
    RESTASIS 0.05%30X 0.4ML OPTH PF; NDC/UPC 23916330; RX; DROPS/Restasis 0.05% 60x0.4 mL OPTH PF; NDC/UPC 23916330; RX
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0563-2021·2021-06-02

    Cardinal Health Recalls Medroxyprogesterone Acetate Injectable Due to Temperature Excursions

    Cardinal Health Inc. is recalling 148 syringes of medroxyprogesterone acetate injectable suspension due to intermittent exposure to temperature excursions during storage.

    Product
    medroxyprogesterone acetate injectable suspension, USP, 150MG/ML 1ML, Rx Only, Distributed by: Greenstone LLC, Peapack, NJ 07977, NDC 59762-4538-02
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0467-2021·2021-06-02

    Cardinal Health Recalls Iron 100 Tablets Due to Temperature Excursions

    Cardinal Health Inc. is recalling Iron 100 with Vitamin C Tablets due to intermittent temperature excursions during storage. The product was distributed in Florida, Georgia, and South Carolina.

    Product
    Iron 100 with Vitamin C Tablets Dietary Supplement 100 Tablets NDC 60258-099-01 Distributed By: Cypress Pharmaceutical, Inc. 135 Industrial Blvd. Madison, MS 39110
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0405-2021·2021-06-02

    Cardinal Health Recalls Synthroid Tablets Due to Temperature Excursions

    Cardinal Health Inc. is recalling 123 bottles of Synthroid (levothyroxine sodium) tablets distributed in Florida, Georgia, and South Carolina due to intermittent temperature excursions during storage.

    Product
    Synthroid (levothyroxine sodium tablets, USP) in all pack sizes, styles and concentrations Rx only Abbott Laboratories North Chicago, IL
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0409-2021·2021-06-02

    Cardinal Health Recalls Lidocaine HCL Visc 2% Due to Temperature Excursions

    Cardinal Health Inc. is recalling 240 bottles of Lidocaine HCL Visc 2% 100ml due to intermittent temperature excursions during storage.

    Product
    LIDOCAINE HCL VISC 2% 100ML; NDC/UPC 50383077504; RX; SOLUTION (USUALLY NOT OTIC, OPTH, NASAL DROPS)
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0394-2021·2021-06-02

    Noven Recalls Daytrana Methylphenidate Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because customer complaints regarding ripped patches and adhesive transfer exceeded action limits.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0447-2021·2021-06-02

    Cardinal Health Recalls Dexamethasone Sodium Phosphate Eye Drops

    Cardinal Health Inc. is recalling 318 droptainers of Dexamethasone Sodium Phosphate 0.1% eye drops due to temperature excursions during storage.

    Product
    DEXAMETH SOD PHOS 0.1% 5ML; NDC/UPC 24208072002; RX; DROPS
    Category
    Drug
    Distribution
    3 states

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