The Recall Desk

Archive

August 2020 recalls

436 recalls were announced in August 2020.

What the numbers show

Critical
25
Severe
99
High
182
Moderate
122
Low
8

Of the 436 recalls this month scored against our rubric, 6% are Critical, 23% are Severe.

Which agencies issued them

201–300 of 436

  • ModerateFDA (Devices)·Z-2797-2020·2020-08-19

    Wright Medical Screw Removal Case Assembly Recalled for Missing Drivers

    Wright Medical Technology is recalling 9 units of the Screw Removal Case Assembly because the kits do not include drivers required to remove specific headless screws.

    Product
    Screw Removal Case Assembly, Part Number 1985BASE - Product Usage: The Wright Medical hardware removal kit is designed to facilitate removal of both plates and screws used in foot and ankle procedures. Along with a complete range of drivers, the kit also features driver handles a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2796-2020·2020-08-19

    Wright Medical Hardware Removal Kit Recalled for Missing Drivers

    Wright Medical Technology is recalling 66 hardware removal kits because they lack the specific drivers needed to remove Dart-Fire 2.5 and 3.0mm Headless screws.

    Product
    Hardware removal kit, Part Number 1985KIT1 - Product Usage: The Wright Medical hardware removal kit is designed to facilitate removal of both plates and screws used in foot and ankle procedures. Along with a complete range of drivers, the kit also features driver handles and a ra
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2802-2020·2020-08-19

    Arrow International Recalls Cannon II Plus Replacement Hub Sets for Labeling Error

    Arrow International Inc is recalling Cannon II Plus Replacement Hub Sets because the lidstock displays an incorrect expiration date, which could lead to the use of expired devices.

    Product
    Cannon II Plus Replacement Hub Set - Product Usage: is indicated for use in the replacement of a Cannon II Plus hub connection assembly that has been damaged.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-1152-2020·2020-08-19

    Indianapolis Fruit Company Recalls Garden Cut Organic Coleslaw Due to Plastic

    Indianapolis Fruit Company is recalling Garden Cut Organic Coleslaw w/ Carrots because pieces of plastic were found in the finished product.

    Product
    Garden Cut Organic Coleslaw w/ Carrots, retail unit packaged in 1lb clam-shell, 4 retail units per wholesale case, retail unit UPC: 053495081016
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2783-2020·2020-08-19

    Flower Orthopedics Recalls Calcaneus Plates Due to Incorrect Material

    Flower Orthopedics is recalling 25 calcaneus plates because they were manufactured with a titanium alloy instead of pure titanium.

    Product
    Calcaneus Plate, Extensile, Medium, Left, Catalog Number CPF 102 - Product Usage: intended to be used for internal fixation of fractures and reconstruction of bones of the rearfoot, including the calcaneus.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2772-2020·2020-08-19

    NeuroLogica OmniTom CT Systems Recalled for Operational Shutdown Issues

    NeuroLogica is recalling 35 OmniTom CT systems due to potential operational issues that could cause inadvertent shutdowns and delays in patient treatment.

    Product
    OmniTom Computed tomography x-ray system, Model NL5000, all NL5000 systems with software version before 05.01.01 - Product Usage: is intended to be used for x-ray computed tomography applications for anatomy that can be imaged in the 40 cm aperture, primarily head and neck.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2791-2020·2020-08-19

    HF Acquisition Recalls STAT KIT Emergency Medical Kits with Missing Narcan Dose

    HF Acquisition Co., LLC is recalling STAT KIT Model 550AI Emergency Medical Kits because they contain one dose of Narcan Nasal spray instead of two.

    Product
    STAT KIT Model 550AI Emergency Medical Kit. P/N: 1010830 containing various products to include Narcan Nasal spray, item number 1010300
    Category
    Medical Device
    Distribution
    39 states
  • ModerateFDA (Devices)·Z-2804-2020·2020-08-19

    Arrow International Recalls NextStep Retrograde Replacement Hub Set Due to Labeling Error

    Arrow International is recalling NextStep Retrograde Replacement Hub Sets because the lidstock displays an incorrect expiration date, which could lead to the use of expired devices.

    Product
    NextStep Retrograde Replacement Hub Set - Product Usage: is indicated for use in the replacement of a NextStep Retrograde hub connection assembly that has been damaged.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1492-2020·2020-08-19

    Teva Recalls Lidocaine Patches Due to Missing Lot and Expiration Dates

    Teva Pharmaceuticals is recalling Lidocaine 5% Patches because individual pouches are missing lot and expiration dates. The recall covers 28,596 cartons distributed nationwide.

    Product
    LIDOCAINE — LIDOCAINE (LIDOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2781-2020·2020-08-19

    Linet AVE 2 Birthing Bed Recalled for Incorrect Manufacturer Labeling

    Linet Americas is recalling 202 AVE 2 Birthing Beds because the Unique Device Identifier (UDI) on the label indicates the incorrect manufacturer.

    Product
    AVE 2 Birthing Bed - Product Usage: is designated to be used by mothers ready for spontaneous vaginal delivery and also as aid to search for individual positions providing relief in all delivery stages including postpartum period. Birthing bed is not intended for use as a general
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1497-2020·2020-08-19

    Golden State Medical Supply Recalls Clobetasol Propionate Cream Due to Content Uniformity Failure

    Golden State Medical Supply Inc. is recalling specific lots of Clobetasol Propionate Cream, USP, 0.05% because the bulk material failed content uniformity testing.

    Product
    Clobetasol Propionate Cream, USP, 0.05%, packaged in a)15g Tubes (NDC 60429-902-15) and b) 45g Tubes (NDC 60429-902-45), Rx Only, Mfd. by: Taro Pharmaceuticals Inc. Brampton, Ontario, Canada, Marketed by: Golden State Medical Supply Inc. Camarillo, CA 93012.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·020-2020 ·2020-08-18

    Faribault Foods Recalls Canned Soup for Misbranding and Undeclared Allergens

    Faribault Foods is recalling 14-oz. cans of Progresso Organic Chicken Noodle Soup because the product contains undeclared milk, soy, beef, and pork.

    Product
    Faribault Foods, Inc. — Faribault Foods Inc. Recalls Canned Soup Product Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V490000·2020-08-18

    BMW X3 and Related Models: Hybrid Battery Short-Circuit Fire Risk

    BMW is recalling hybrid X3, 330e, X5, and 2020 MINI Countryman SE models with loose battery welds that may cause short-circuits and fire. All vehicles have already been remedied.

    Product
    MINI — MINI, BMW COUNTRYMAN, X3, X5, 330E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V487000·2020-08-18

    KME Fire Trucks Recalled for Excessively Bright LED Lights

    KME is recalling 38 fire trucks because certain LED lights are too bright, potentially blinding other drivers and increasing crash risk.

    Product
    KME — KME PREDATOR SS RESCUE, PREDATOR PANTHER AERIAL, COMMERCIAL PUMPER, PREDATOR SS AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V489000·2020-08-18

    GM Recalls 2020 Chevrolet Corvette for Unlatched Front Trunk Lid Risk

    General Motors is recalling 2020 Chevrolet Corvette vehicles because the front trunk lid can be driven while unlatched, potentially opening at speed and obstructing the driver's view.

    Product
    CHEVROLET — CHEVROLET CORVETTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V488000·2020-08-18

    Forest River Recalls Motorhomes With Potential Rear Light Malfunctions

    Forest River is recalling specific 2017-2020 motorhomes because a damaged Power Distribution Module may cause rear marker, brake, or turn signal lights to stop working.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN BERKSHIRE, CROSS COUNTRY, SPORTSCOACH, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E055000·2020-08-18

    Watson & Chalin Recalls SL2065 Lift Axle Suspension Systems

    Watson & Chalin is recalling SL2065 steerable lift axle suspension systems because short pivot cap screws may separate, creating road hazards and increasing crash risk.

    Product
    SUSPENSION:MULTIPLE AXLE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V480000·2020-08-14

    Mercedes-Benz Recalls 2020 GLB 250 for Rear Spoiler Welding Defect

    Mercedes-Benz is recalling 2020 GLB 250 vehicles because the rear spoiler may not be welded correctly, posing a road hazard if it detaches.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V483000·2020-08-14

    2021 BMW X5 and X6 Vehicles Recalled for Defective Tires

    BMW is recalling 2021 X5 and X6 models equipped with certain Pirelli tires. The tires may have damaged inner layers that can cause rapid pressure loss while driving, affecting vehicle control.

    Product
    BMW — BMW X5, X6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V485000·2020-08-14

    Freightliner Custom Chassis Trucks Recalled for Instrument Panel Glare

    Daimler Trucks North America is recalling certain 2015-2019 Freightliner Custom Chassis trucks because the instrument panel brightness cannot be adjusted, potentially causing glare at night.

    Product
    FCCC — FCCC XCM, XCS, XCL, XCR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V477000·2020-08-14

    Motorhome Recall: Defective Wiring Harness May Affect Side Air Bag Deployment

    Forest River is recalling certain 2020-2021 motorhomes with swivel seats due to incorrectly routed wiring harnesses that could damage the side air bag system, risking inadvertent or failed deployment in a crash.

    Product
    COACHMEN — COACHMEN, FOREST RIVER, DYNAMAX GALLERIA, PRISM, FORESTER, SUNSEEKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V476000·2020-08-13

    BMW Recalls Motorcycles Due to Front Brake Caliper Fluid Leaks

    BMW is recalling specific 2019-2020 motorcycles because front brake calipers may leak fluid, potentially reducing brake performance and increasing crash risk.

    Product
    BMW — BMW R 1250 RT, R 1250 GS ADVENTURE, R 1250 GS, S 1000 RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V475000·2020-08-13

    Chrysler Recalls Ram 1500 and Jeep Grand Cherokee for Engine Stall Risk

    Chrysler is recalling 2014-2018 Ram 1500 and 2014-2016 Jeep Grand Cherokee diesel vehicles because a sensor defect may cause the engine to stall, increasing crash risk.

    Product
    RAM — RAM, JEEP 1500, GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1464-2020·2020-08-12

    Pathway To Wellness CBD Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling 100 bottles of Pathway To Wellness CBD Oil due to elevated levels of undeclared lead. The product was sold nationwide via internet and retail channels.

    Product
    Pathway To Wellness, CBD Oil, Premium Hemp Oil Drops, Natural, 1000MG CBD, 1 FL OZ (30 ML) bottles, Distributed by: Pathway to Wellness
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1474-2020·2020-08-12

    Tasty Drops CBD Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Tasty Drops CBD oil bottles due to elevated levels of undeclared lead. The product was sold nationwide via internet and retail channels.

    Product
    Tasty Drops, Hemp Oil Extract, Spearmint, 1000MG CBD, 1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 8 02991 76539 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1477-2020·2020-08-12

    Tasty Drops Hemp Oil Extract Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract due to elevated levels of undeclared lead. Consumers should stop using the product.

    Product
    Tasty Drops, Hemp Oil Extract, Vanilla, 1500MG CBD,1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29086 6
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2734-2020·2020-08-12

    Smiths Medical Medfusion Syringe Pump Recall for Inaccurate Dose Delivery

    Smiths Medical is recalling Medfusion Syringe Pump Model 4000 units due to a risk of inaccurate drug delivery following interrupted bolus or loading doses.

    Product
    Medfusion Syringe Pump Model 4000; Software Versions V1.5.0, V1.5.1, V1.6.0, and V1.6.1
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Drugs)·D-1455-2020·2020-08-12

    A Clean Choice CBD Tincture Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling A Clean Choice CBD tinctures due to elevated levels of undeclared lead. Consumers should stop using the product.

    Product
    A Clean Choice CBD, Hemp Oil Extract Tincture, Strawberry Creme, 1000mg, 1 fl oz (30 ml) bottles, Made in Michigan for A Clean Choice, A Division of A Clean Cigarette, Inc., 3055 Bay Rd Suite 1, Saginaw, MI 48603
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1450-2020·2020-08-12

    Tasty Drops Hemp Oil Extract Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract because it contains elevated levels of undeclared lead.

    Product
    Tasty Drops Hemp Oil Extract, Vanilla, 1 FL. OZ (30ML) bottles, 300MG CBD, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 8 02991 76471 4
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1453-2020·2020-08-12

    Hemp Extract Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling 496 bottles of Made by Hemp 1000MG Hemp Extract due to elevated levels of undeclared lead.

    Product
    Made by Hemp 1000MG Hemp Extract, Strawberry Creme, 1 OZ (30 ML) bottles, Dist by: MHR Brands, Jenison, MI, UPC 8 02991 76554 4
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1473-2020·2020-08-12

    Tasty Drops CBD Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Tasty Drops CBD oil due to elevated levels of undeclared lead. Consumers should stop using the product.

    Product
    Tasty Drops, Hemp Oil Extract, Spearmint, 500MG CBD, 1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29081 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1459-2020·2020-08-12

    BC Hemp Co. CBD Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling BC Hemp Co. CBD Oil bottles due to elevated levels of undeclared lead.

    Product
    BC Hemp Co., Full Spectrum Hemp Extract, CBD Oil, Spearmint, 500mg CBD, 1 FL. OZ (30 ML) bottles, Distributed by: B.C. Hemp Co., LLC, P.O. Box 156, Eau Claire, MI 49111
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1470-2020·2020-08-12

    Tasty Drops CBD Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Tasty Drops CBD oil bottles due to elevated levels of undeclared lead.

    Product
    Tasty Drops, Hemp Oil Extract, Berry, 500MG CBD, 1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29083 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2716-2020·2020-08-12

    CareFusion Alaris System PC Unit Model 8000 Recall for Cleaning Agent Damage

    CareFusion 303, Inc. is recalling Alaris System PC Unit Model 8000 infusion pumps because cleaning agents may damage connectors, causing therapy interruptions.

    Product
    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1472-2020·2020-08-12

    Tasty Drops Hemp Oil Extract Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract because the product contains elevated levels of undeclared lead.

    Product
    Tasty Drops, Hemp Oil Extract, Natural, 1500MG CBD, 1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29088 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2768-2020·2020-08-12

    Beacon EUS Access System Needle Recalled Due to Cannula Detachment

    Covidien is voluntarily recalling 375 units of the Beacon EUS Access System Preloaded Access 90-degree Needle because the cannula may detach during procedures.

    Product
    Beacon EUS Access System Preloaded Access 90degree Needle sterile, single-use, endoscopic ultrasound device consisting of a sharp stylet and an 18.5-gauge, echo-enhanced, tip-shaped, nitinol cannula intended to pierce tissue and then act as an access channel to facilitate guidew
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-1486-2020·2020-08-12

    Yusef Tropical Lip Moisturizer Recalled for Superpotent Meradimate Ingredient

    Yusef Manufacturing Laboratories is recalling Tropical Lip Moisturizer, SPF 30, because the beginning of the batch is approximately 25% superpotent for the active ingredient Meradimate.

    Product
    Tropical Lip Moisturizer, SPF 30, UVA/UVB Lip Protection, Active Ingredients: Oxybenzone 5%, Octisalate 5%, Octinoxate 7.5%, Meradimate 5%, Made in USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2769-2020·2020-08-12

    Beacon EUS Access System Needle Recalled Due to Cannula Detachment

    Covidien is voluntarily recalling 269 Beacon EUS Access System needles because the cannula detached during procedures in three reported cases.

    Product
    Beacon EUS Access System Preloaded Access 135degree Needle sterile, single-use, endoscopic ultrasound device consisting of a sharp stylet and an 18.5-gauge, echo-enhanced, tip-shaped, nitinol cannula intended to pierce tissue and then act as an access channel to facilitate guide
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2750-2020·2020-08-12

    GE Healthcare Recalls CARESCAPE ONE Monitors Due to Alarm Failure Risk

    GE Healthcare is recalling 8,414 CARESCAPE ONE patient monitors because they may fail to provide visual and audible alarms for Ventricular Fibrillation when docked to specific host monitors.

    Product
    CARESCAPE ONE, Physiological Patient Monitor - Product Usage: is both a multi-parameter physiological patient monitor and an accessory to a multi-parameter patient monitor intended for use in multiple areas and intra-hospital transport within a professional healthcare facility.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1465-2020·2020-08-12

    Michigan Herbal Remedies Recalls CBD Hemp Oil Due to Lead Contamination

    Michigan Herbal Remedies is recalling 25 bottles of SP Berry CBD hemp oil because the product contains elevated levels of undeclared lead.

    Product
    SP, hemp oil, Berry, 300MG CBD,1 FL. OZ (30 ML) bottles, Distributed by: The Spiffy Piff
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1471-2020·2020-08-12

    Tasty Drops Hemp Oil Extract Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract because the product contains elevated levels of undeclared lead.

    Product
    Tasty Drops, Hemp Oil Extract, Berry, 1500MG CBD, 1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29087 3
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1452-2020·2020-08-12

    Hemp Extract Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling 486 bottles of Made by Hemp 1000MG Hemp Extract due to elevated levels of undeclared lead.

    Product
    Made by Hemp 1000MG Hemp Extract, Mojito Lime, 1 OZ (30 ML) bottles, Dist by: MHR Brandsl, Jenison, M,I UPC 8 02991 76552 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1476-2020·2020-08-12

    Tasty Drops CBD Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Tasty Drops CBD oil bottles due to elevated levels of undeclared lead.

    Product
    Tasty Drops, Hemp Oil Extract, Vanilla, 500MG CBD, 1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29082 8
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1478-2020·2020-08-12

    BC Hemp Co. CBD Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling 50 bottles of BC Hemp Co. CBD Oil due to elevated levels of undeclared lead.

    Product
    BC Hemp Co., Full Spectrum Hemp Extract, CBD Oil , Berry Blast, 1000MG CBD, 1 FL. OZ (30ML) bottles, Distributed by: B.C. Hemp Co., LLC, P.O. Box 156, Eau Claire, MI 49111
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1489-2020·2020-08-12

    Summitt Labs Recalls KORE Organic CBD Oil Due to Lead Contamination

    Summitt Labs is recalling 236 bottles of KORE Organic CBD Oil Watermelon 15mg due to elevated lead levels. The product was distributed nationwide in the USA.

    Product
    KORE ORGANIC CBD Oil Watermelon 15mg*, 30 mL dropper bottles, Handcrafted By Summitt Labs, UPC 8 5765000812 8, www.KOREORGANIC.com 833.810.KORE.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1475-2020·2020-08-12

    Tasty Drops CBD Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Tasty Drops CBD oil bottles due to elevated levels of undeclared lead. Consumers should stop using the product.

    Product
    Tasty Drops, Hemp Oil Extract, Spearmint, 1500MG CBD,1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29085 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1479-2020·2020-08-12

    BC Hemp Co. CBD Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling 25 bottles of BC Hemp Co. CBD Oil due to elevated levels of undeclared lead.

    Product
    BC Hemp Co., Full Spectrum Hemp Extract, CBD Oil, Natural, 1000MG CBD, 1 FL. OZ (30 ML) bottles, Distributed by: B.C. Hemp Co., LLC, P.O. Box 156, Eau Claire, MI 49111
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1460-2020·2020-08-12

    Michigan Herbal Remedies Recalls Healthy Hemp Drops Due to Lead Contamination

    Michigan Herbal Remedies is recalling Goodness Gurus Healthy Hemp Drops because the product contains elevated levels of undeclared lead.

    Product
    Goodness Gurus, Healthy Hemp Drops, 500MG/Berry, 1 FL. OZ bottles, Distributed by: Goodness Gurus, Inc., Carlisle, PA, UPC 6 53341 99271 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1466-2020·2020-08-12

    Michigan Herbal Remedies Recalls CBD Hemp Oil Due to Lead Contamination

    Michigan Herbal Remedies is recalling 25 bottles of 300mg CBD hemp oil because the product contains elevated levels of undeclared lead.

    Product
    SP, hemp oil, Spearmint, 300MG CBD, 1 FL. OZ (30 ML) bottles, Distributed by: The Spiffy Piff
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1484-2020·2020-08-12

    Mylan Recalls Daptomycin Injection Due to Particulate Matter

    Mylan Institutional LLC is recalling 18,480 vials of Daptomycin for Injection due to the presence of particulate matter. The product is distributed nationwide.

    Product
    DAPTOMYCIN — DAPTOMYCIN (DAPTOMYCIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1449-2020·2020-08-12

    Tasty Drops Hemp Oil Extract Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract due to elevated levels of undeclared lead. Consumers should stop using the product.

    Product
    Tasty Drops Hemp Oil Extract, Spearmint, 1 FL. OZ (30ML) bottles, 300MG CBD, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 8 02991 76472 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2758-2020·2020-08-12

    Siemens Ysio Max X-Ray System Recalled for Software Defects

    Siemens Medical Solutions is recalling 512 Ysio Max X-ray systems due to software issues that may cause collisions or incorrect diagnostic images.

    Product
    SIEMENS Healthineers Ysio Max - Interventional Fluoroscopic X-Ray System, Model: 10762470 - Product Usage: is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1503-2020·2020-08-12

    Spartan Chemical Recalls Lemon Blossom Hand Sanitizer Due to Microbial Contamination

    Spartan Chemical Co Inc is recalling Lemon Blossom Hand Sanitizer because testing found positive microbial contamination in the product.

    Product
    Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1% - antimicrobial), For Institutional and Industrial Use Only, a) foamyiQ 42.27 oz/1250 mL cartridge, UPC code: 7 53727 26454 4; b) Lite 'n Foamy 1 gallon/3.79 L container UPC code: 7 53727 26113 0, Spartan Chemical Company,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1482-2020·2020-08-12

    Herbzeedy Hemp Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling 33 bottles of Herbzeedy Hemp Oil due to elevated levels of undeclared lead. The product was sold nationwide via internet and retail channels.

    Product
    Herbzeedy, Hemp Oil Full Spectrum, Natural, 1500 MG CBD, 1 FL OZ (30 ML) bottles, Distributed by: Herbzeedy, Statesboro, GA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1469-2020·2020-08-12

    Acadia Farms Serenity Hemp Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Acadia Farms Serenity Hemp Oil bottles due to elevated levels of undeclared lead.

    Product
    Acadia Farms, Serenity, soothing mint, 300 MG Hemp Oil, 1 Fl OZ (30 ML) bottles, Distributed by: Acadia Farms, Rehobeth, Massachusetts
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1454-2020·2020-08-12

    A Clean Choice CBD Tincture Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling A Clean Choice CBD Tincture bottles due to elevated levels of undeclared lead.

    Product
    A Clean Choice CBD, Hemp Oil Extract Tincture, French Vanilla, 1000 mg, 1 fl oz (30 ml) bottles, Made in Michigan for A Clean Choice, A Division of A Clean Cigarette, Inc., 3055 Bay Road Suite 1, Saginaw, MI 48603
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1457-2020·2020-08-12

    BC Hemp Co. CBD Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling 25 bottles of BC Hemp Co. CBD Oil due to elevated levels of undeclared lead.

    Product
    BC Hemp Co., Full Spectrum Hemp Extract, CBD Oil, Berry Blast, 500mg CBD, 1 FL. OZ (30 ML) bottles, Distributed by: B.C. Hemp Co., LLC, P.O. Box 146, Eau Claire, MI 49111
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1463-2020·2020-08-12

    Javan CBD Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Javan CBD Oil bottles due to elevated levels of undeclared lead. The product was sold nationwide via internet and retail.

    Product
    Javan Anti Aging and Wellness Institute, CBD Oil, Full Spectrum Hemp Oil, Spearmint, 300MG CBD, 1 FL. OZ (30 ML) bottles, Dist by: Javan Wellness LLC, 1445 Church St NW Unit 24, Washington, DC 20005
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1462-2020·2020-08-12

    Herbzeedy Hemp Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Herbzeedy Hemp Oil Full Spectrum bottles due to elevated levels of undeclared lead.

    Product
    Herbzeedy, Hemp Oil Full Spectrum, Natural, 500 MG CBD, 1 FL OZ (30 ML) bottles, Distributed by: Herbzeedy, Statesboro, GA
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1480-2020·2020-08-12

    Michigan Herbal Remedies Recalls Goodness Gurus Hemp Drops for Lead Contamination

    Michigan Herbal Remedies is recalling 50 bottles of Goodness Gurus Healthy Hemp Drops due to elevated levels of undeclared lead.

    Product
    Goodness Gurus, Healthy Hemp Drops Full Strength, 1000 MG/Spearmint, 1 FL. OZ bottles, Distributed by: Goodness Gurus, Inc., Carlisle, PA, UPC 53341 99311 3
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1456-2020·2020-08-12

    A Clean Choice CBD Tincture Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling A Clean Choice CBD tinctures because they contain elevated levels of undeclared lead.

    Product
    A Clean Choice CBD, Hemp Oil Extract Tincture, Sweet Mint, 500mg, 1 fl oz (30 ml) bottles, Made in Michigan for A Clean Choice, A Division of A Clean Cigarette, Inc., 3055 Bay Rd Suite 1, Saginaw, MI 48603
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1447-2020·2020-08-12

    Tasty Drops Hemp Oil Extract Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract due to elevated levels of undeclared lead. Consumers should stop using the product.

    Product
    Tasty Drops Hemp Oil Extract, Natural, 1 FL. OZ (30ML) bottles, 500mg CBD, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29084 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1451-2020·2020-08-12

    Michigan Herbal Remedies Recalls Hemp Extract Due to Lead Contamination

    Michigan Herbal Remedies is recalling 495 bottles of Made by Hemp 1000MG Hemp Extract because the product contains elevated levels of undeclared lead.

    Product
    Made by Hemp 1000MG Hemp Extract, French Vanilla, 1 OZ (30 ML) bottles, Dist by: MHR Brands, Jenison, MI, UPC 8 02991 76553 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1458-2020·2020-08-12

    BC Hemp Co. CBD Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling 72 bottles of BC Hemp Co. CBD Oil due to elevated levels of undeclared lead.

    Product
    BC Hemp Co., Full Spectrum Hemp Extract, CBD Oil, Natural 500MG CBD, 1 FL. OZ (30 ML) bottles, Distributed by: B.C. Hemp Co., LLC, P.O. Box 156, Eau Claire, MI 49111
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1467-2020·2020-08-12

    Recovery Releaf CBD Oil Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Recovery Releaf Pure CBD Oil due to elevated levels of undeclared lead. Consumers should stop using the product.

    Product
    Recovery Releaf, Pure CBD Oil, Vanilla, 1000MG, 25MG per serving, 1 fl. oz (30 ml) bottles,Distributed by: Recovery Releaf, West Palm Beach, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1468-2020·2020-08-12

    Acadia Farms Equilibrium Vermont Maple Hemp Oil Recalled for Lead Contamination

    Michigan Herbal Remedies is recalling Acadia Farms Equilibrium Vermont Maple Hemp Oil bottles due to elevated levels of undeclared lead.

    Product
    Acadia Farms, Equilibrium, vermont maple, 300 MG Hemp Oil, 1 Fl OZ (30 ML) bottles, Distributed by: Acadia Farms, Rehobeth, Massachusetts
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1461-2020·2020-08-12

    Hemp Drops Recalled for Undeclared Lead Contamination

    Michigan Herbal Remedies is recalling Goodness Gurus Healthy Hemp Drops because the product contains elevated levels of undeclared lead.

    Product
    Goodness Gurus, Healthy Hemp Drops, 500MG/Spearmint, 1 FL. OZ bottles, Distributed by: Goodness Gurus, Inc., Carlisle, PA, UPC 6 53341 99261 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1448-2020·2020-08-12

    Tasty Drops Hemp Oil Extract Recalled for Undeclared Lead

    Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract due to elevated levels of undeclared lead.

    Product
    Tasty Drops Hemp Oil Extract, Berry, 1 FL. OZ (30ML) bottles, 300MG CBD, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 8 02991 76469 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1481-2020·2020-08-12

    Michigan Herbal Remedies Recalls Goodness Gurus Hemp Drops for Lead Contamination

    Michigan Herbal Remedies is recalling Goodness Gurus Healthy Hemp Drops due to elevated levels of undeclared lead. The product was sold nationwide via internet and retail channels.

    Product
    Goodness Gurus, Healthy Hemp Drops, 1500 MG/Spearmint, 1 FL. OZ bottles, Distributed by: Goodness Gurus, Inc., Carlisle, PA, UPC 6 53341 99411 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2766-2020·2020-08-12

    Medline Recalls Endoscopic Cleaning Brushes Due to Detachment Risk

    Medline Industries Inc is recalling 1,400 endoscopic cleaning brushes because the brush may detach during use. The recall covers specific models and lots distributed nationwide.

    Product
    Endoscopic Cleaning Brush - Product Usage: Endoscopic cleaning brushes are single use devices intended to clean the interior of endoscopes after endoscopy procedures. The brush is threaded through the biopsy valve and pulled through the interior of the endoscope to remove debris.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2736-2020·2020-08-12

    CareFusion Alaris Pump Module Model 8100 Recalled for Broken Platen Elements

    CareFusion 303, Inc. is recalling Alaris Pump Module Model 8100 units because broken platen elements can cause inaccurate fluid delivery, leading to over-infusion, free-flow, or under-infusion.

    Product
    Alaris Pump Module Model 8100
    Category
    Medical Device
    Distribution
    54 states
  • HighFDA (Devices)·Z-2721-2020·2020-08-12

    CareFusion Alaris EtCO2 Module Recall Due to Cleaning Agent Damage

    CareFusion 303, Inc. is recalling Alaris EtCO2 Module Model 8300 units because cleaning agents may damage connectors, potentially interrupting infusion therapy or monitoring.

    Product
    Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2741-2020·2020-08-12

    CareFusion Alaris System PC Unit Model 8015 Infusion Pump Recall

    CareFusion is recalling Alaris System PC Unit Model 8015 infusion pumps because loose or missing screws may cause power loss and therapy interruption.

    Product
    Alaris System PC Unit Model 8015. modular infusion pump and monitoring system
    Category
    Medical Device
    Distribution
    55 states
  • HighFDA (Devices)·Z-2735-2020·2020-08-12

    Smiths Medical Medfusion Syringe Pump Recall for Inaccurate Delivery

    Smiths Medical is recalling Medfusion Syringe Pump Model 3500 units because inaccurate delivery can occur after an interrupted Bolus or Loading dose.

    Product
    Medfusion Syringe Pump Model 3500, Software Version V6.0. Infusion pump.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2723-2020·2020-08-12

    CareFusion Alaris Auto ID Module Recall Due to Cleaning Agent Damage

    CareFusion is recalling Alaris Auto ID Modules because cleaning agents may damage connectors, causing infusion interruptions and therapy stops.

    Product
    Alaris Auto ID Module Model 8600, a modular infusion pump and monitoring system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2764-2020·2020-08-12

    Boston Scientific Recalls Captiflex Snares Due to Potential Cutting Failure

    Boston Scientific is recalling specific lots of Captiflex Snares because they may fail to cut polyps, potentially causing tissue damage or bleeding.

    Product
    Captiflex Snares, Single-Use Polypectomy Snare consists of a flexible wire cable and loop which can be extended and retracted from the snares flexible outer sheath using a three-ring handle. The inner diameter of the sheath is PolyGlide" Lubricant coated to provide minimal frict
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2743-2020·2020-08-12

    Normand-Info Remisol Advance Software Recall for Erroneous Lab Results

    Normand-Info is recalling Remisol Advance software version 1.12 because it deletes specific white blood cell and platelet results, potentially leading to erroneous data.

    Product
    Remisol Advance running Software Version 1.12 The Normand Info Remisol Advance Data Manager collects and manages data and workflow for 128 connections (Beckman Coulter Instruments, automations, LIS &). It can also be connected to a host system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2761-2020·2020-08-12

    Boston Scientific Recalls Captivator Polypectomy Snares Due to Cutting Defect

    Boston Scientific is recalling Captivator Polypectomy Snares because they may fail to cut and remove polyps, potentially causing tissue damage or bleeding.

    Product
    Captivator Polypectomy Snare, Single-Use Polypectomy Snare consists of a flexible wire cable and loop which can be extended and retracted from the snare s flexible outer sheath using a three-ring handle. The inner diameter of the sheath is PolyGlide" Lubricant coated to provide
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2756-2020·2020-08-12

    Siemens Luminos Agile Max Recalled for Software Collision and Image Errors

    Siemens Medical Solutions is recalling 477 Luminos Agile Max units due to software defects that may cause system collisions or incorrect diagnostic images.

    Product
    SIEMENS Healthineers Luminos Agile Max Model: 10762472 - Product Usage: is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2765-2020·2020-08-12

    Boston Scientific Recalls Captivator Polypectomy Snares Due to Cutting Defect

    Boston Scientific is recalling Captivator Polypectomy Snares because they may fail to cut and remove polyps, potentially causing tissue damage or bleeding.

    Product
    Captivator Polypectomy Snare, Single-Use Polypectomy Snare consists of a flexible wire cable and loop which can be extended and retracted from the snare s flexible outer sheath using a three-ring handle. The inner diameter of the sheath is PolyGlide" Lubricant coated to provide
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2762-2020·2020-08-12

    Boston Scientific Recalls Captivator Polypectomy Snares Due to Cutting Failure

    Boston Scientific is recalling Captivator Polypectomy Snares because they may fail to cut and remove polyps, potentially causing prolonged procedures or tissue damage.

    Product
    Captivator Polypectomy Snare, Single-Use Polypectomy Snare consists of a flexible wire cable and loop which can be extended and retracted from the snare s flexible outer sheath using a three-ring handle. The inner diameter of the sheath is PolyGlide" Lubricant coated to provide
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·20165·2020-08-12

    Active Brands Recalls Sweet Protection Bicycle Helmets Due to Head Injury Risk

    Active Brands is recalling about 300 Sweet Protection bicycle helmets because they do not meet U.S. safety standards, posing a risk of head injury.

    Product
    Sweet Protection brand Ripper Jr., Ripper MIPS Jr., and Ripper MIPS bicycle helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2745-2020·2020-08-12

    Mako Hip End Effector Recalled for Potential Bone Preparation Discrepancy

    Mako Surgical Corporation is recalling 12 units of Mako Hip End Effectors due to a characterization issue that may cause discrepancies during bone preparation in certain Mako Total Hip procedures.

    Product
    Mako Hip End Effector, Variable Angle Catalog Number: 206967 GTIN:00848486022167
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-2757-2020·2020-08-12

    Siemens Uroskop Omnia Max Recalled for Software Collision and Image Errors

    Siemens is recalling 194 Uroskop Omnia Max units due to software issues that may cause system collisions or incorrect diagnostic images.

    Product
    SIEMENS Healthineers Uroskop Omnia max Model: 10762473 - Product Usage: is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1049-2020·2020-08-12

    Dietary Supplements Recalled for Undeclared Soy Allergen

    Provident Nutraceutical is recalling 95 bottles of various branded dietary supplements because they may contain undeclared soy.

    Product
    Dietary supplements, 60 capsules, UPC 15033-61832, Product # 832060, labeled under the following brands and product names, packaged in white plastic bottle with black plastic lid: 1. Aspire Rejuvenation Nutraceuticals, Tranquility PM, Mfg for: Aspire Rejuvenation Nutraceut
    Category
    Food
    Distribution
    5 states
  • HighNHTSA·20V474000·2020-08-12

    2021 Winnebago Revel motorhomes recalled for detaching alternator belt

    Winnebago is recalling certain 2021 Revel motorhomes. The auxiliary alternator belt may wear and detach, which could cause loss of power steering control and increase the risk of crashes.

    Product
    WINNEBAGO — WINNEBAGO REVEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1163-2020·2020-08-12

    Topway Enterprises Recalls Salmon Cut and Packaged in Styrofoam Cases

    Topway Enterprises is recalling approximately 16,700 lbs of cut salmon packaged in Styrofoam cases due to potential contamination with Listeria monocytogenes.

    Product
    Salmon cut and packaged in Styrofoam case approximately 19 kg per case
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1164-2020·2020-08-12

    Topway Enterprises Recalls Tuna for Potential Listeria Contamination

    Topway Enterprises is recalling approximately 1,300 lbs of cut tuna due to potential Listeria monocytogenes contamination. The product was distributed in five southern states.

    Product
    Tuna cut and packaged in Styrofoam case approximately 19 kg per case
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1048-2020·2020-08-12

    Whole Foods Recalls Chantilly Key Lime Tartlets for Undeclared Almonds

    Whole Foods Market is recalling Chantilly Key Lime Tartlets in New England states due to potential undeclared almonds.

    Product
    Chantilly Key Lime Tartlets Net Wt 1 oz. individually packaged in plastic clamshell containers with Whole Foods Market scale labels, a PLU code of 268564
    Category
    Food
    Distribution
    5 states
  • HighCPSC·20162·2020-08-12

    Intertex Recalls B-Air, BlueDri, and Soleaire Blowers Due to Fire Hazard

    Intertex is recalling approximately 189,000 B-Air, BlueDri, BlueDri Pro, and Soleaire blowers because unprotected side outlets pose a fire hazard.

    Product
    B-Air, BlueDri, BlueDri Pro and Soleaire Blowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide

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