The Recall Desk

Archive

December 2020 recalls

500 recalls were announced in December 2020.

What the numbers show

Critical
15
Severe
129
High
252
Moderate
97
Low
7

Of the 500 recalls this month scored against our rubric, 3% are Critical, 26% are Severe.

201–300 of 500

  • HighCPSC·21057·2020-12-23

    GSK Recalls Five Excedrin Brands Due to Child-Resistant Packaging Defects

    GSK Consumer Healthcare is recalling five Excedrin brands because some bottles have holes in the bottom, posing a risk of poisoning to children.

    Product
    Excedrin Migraine Caplets, Excedrin Migraine Geltabs, Excedrin Extra Strength Caplets, Excedrin PM Headache Caplets, and Excedrin Tension Headache Caplets
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0171-2021·2020-12-23

    Market of Choice Recalls Sour Cherry Baked Brie for Almond Mislabeling

    Market of Choice Inc. is recalling Sour Cherry Baked Brie because the scale label failed to list almond as an ingredient.

    Product
    Market of Choice brand Sour Cherry Baked Brie is wrapped in a plastic shrink wrap and has a white adhesive store label. UPC 0 217241 414996. The label is read in parts: "***SOUR CHERRY BAKED BRIE*** Puff Pastry (wheat flour, niacin, reduced iron, thiamine mononitrate, riboflav
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·20V811000·2020-12-23

    GM Recalls Bolt EV and Other Vehicles for Seat Belt Attachment Defect

    General Motors is recalling multiple 2020-2021 vehicles due to incorrect bolts used to secure seat belts. Improperly fastened seat belts may fail to properly restrain occupants in a crash.

    Product
    CHEVROLET — CHEVROLET, CADILLAC, GMC SUBURBAN, ESCALADE NA, COLORADO, SILVERADO 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0633-2021·2020-12-23

    Maquet Cardiovascular Recalls HLS Set Advanced Due to Sterility Breach

    Maquet Cardiovascular is recalling the HLS Set Advanced because of breaches in the product's sterility barrier. The device is used with the CARDIOHELP system for cardiac and pulmonary support.

    Product
    HLS Set Advanced, Model: BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Product Code/Part Number: 70105.2794 - Product Usage: These devices are used with the CARDIOHELP system in order to provide extracorporeal circulation for cardiac support and/or pulmonary support.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0623-2021·2020-12-23

    Biomet OSS Polyethylene Tibial Bushing Recalled for Sterile Seal Breach

    Biomet is recalling specific lots of OSS Polyethylene Tibial Bushings because a breach in the sterile seal could lead to loss of sterility.

    Product
    OSS Polyethylene Tibial Bushing, Item number 150476 - Product Usage: intended for use in limb salvage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0588-2021·2020-12-23

    BD PrecisionGlide Needles Recalled Due to Blood Contamination

    Becton Dickinson is recalling BD PrecisionGlide needles because blood was found on the cannulas, posing a potential infection risk if not noticed by clinicians.

    Product
    BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) REF 305106 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampoules and parts of the body below the surface of the skin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0622-2021·2020-12-23

    Biomet M/H Modular Stem Recalled for Potential Sterile Seal Breach

    Biomet, Inc. is recalling 7,428 units of the M/H Modular Stem (Item 13-104756) because a breach in the sterile seal could lead to loss of sterility.

    Product
    M/H MODULAR STEM, Item number 13-104756 - Product Usage: intended for use in limb salvage procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0570-2021·2020-12-23

    Zimmer Biomet Recalls Polaris Spinal System Screws for Labeling Update

    Zimmer Biomet is updating instructions for Polaris and Cypher spinal screws to warn against using them with direct current stimulation due to construct failure risks.

    Product
    Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System, Thoracolumbosacral pedicle screw system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0634-2021·2020-12-23

    Roche Recalls Tina-quant C-Reactive Protein Gen.3 Reagents Due to Cross-Contamination

    Roche is recalling Tina-quant C-Reactive Protein Gen.3 reagents due to cross-contamination causing invalid calibrations and low quality control recovery.

    Product
    Tina-quant C-Reactive Protein Gen.3, Catalog number 05172373190 - Product Usage: the in vitro quantitative determination of CRP in human serum and plasma on Roche automated clinical chemistry analyzers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0154-2021·2020-12-23

    Taro Recalls Kroger Clotrimazole Cream Due to Impurity

    Taro Pharmaceuticals is recalling Kroger Athlete's Foot Cream because an unknown degradation impurity was detected slightly above the specification limit.

    Product
    KROGER — KROGER (CLOTRIMAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0637-2021·2020-12-23

    Boston Scientific Recalls EKOS Control System Units Due to RF Board Failure

    Boston Scientific is replacing 90 EKOS Control System 4.0 units in Latin America and the EU to prevent internal RF board failures at lower temperatures.

    Product
    EKOS Control System (CU) 4.0. UPN 600-40500 The EkoSonic MACH4 Endovascular (EKOS) System consists of a single use Infusion Catheter and Ultrasonic Core, and a reusable Control Unit 4.0. The device delivers the physician-specified fluids and ultrasound to the intravascular t
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0146-2021·2020-12-23

    Zydus Recalls Lansoprazole Tablets for Failed Dissolution Specifications

    Zydus Pharmaceuticals is recalling 22,848 cartons of Lansoprazole 30 mg tablets nationwide because they failed to meet dissolution specifications.

    Product
    LANSOPRAZOLE — LANSOPRAZOLE (LANSOPRAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0176-2021·2020-12-23

    Chef Mitch Maier's Black Garlic Sauce Recalled for Potential Mold Growth

    Out of the Kitchen, LLC is recalling specific bottles of Chef Mitch Maier's Black Garlic Sauce because they may develop mold before the expiration date.

    Product
    Chef Mitch Maier's Black Garlic Sauce. Net Wt. 16 oz. (473g). UPC 8 60248-00253 8.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0169-2021·2020-12-23

    Hikma Recalls Sodium Chloride Injection Vials Due to pH Failures

    Hikma Pharmaceuticals is recalling 1.3 million vials of Sodium Chloride Injection USP 0.9% because pH test results were out of specification.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0159-2021·2020-12-23

    Taro Recalls Clotrimazole Cream Due to Unknown Degradation Impurity

    Taro Pharmaceuticals is recalling specific lots of Clotrimazole Cream USP 1% because an unknown degradation impurity was detected slightly above the specification limit.

    Product
    Athlete's Foot Cream, Clotrimazole Cream USP, 1%, Antifungal Cream, NET WT 1 oz (30 g), Distributed by: Taro Pharmaceuticals U.S.A. Inc. Hawthorne, NY 10531. Made in Canada. UPC 3 51672 20022 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0156-2021·2020-12-23

    Taro Recalls Rite Aid Clotrimazole Cream Due to Impurity

    Taro Pharmaceuticals is recalling Rite Aid Clotrimazole Cream because an unknown degradation impurity was detected slightly above the specification limit.

    Product
    RiteAid Pharmacy RIngworm Cream, Clotrimazole Cream USP, 1%, Antifungal NET W 0.5 oz. (14.2g), Distributed by: Rite Aid, 30 Hunter Lane, Camp Hill, PA 17011 Made in Canada. UPC 0 11822 53812 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0167-2021·2020-12-23

    AvKARE Recalls Sildenafil Tablets Due to Packaging Mix-Up with Trazodone

    AvKARE Inc. is recalling 38,715 bottles of Sildenafil 100 mg tablets because they were inadvertently packaged with trazodone at a third-party facility.

    Product
    Sildenafil Tablets USP 100 mg, Rx Only, 100-count Bottle, Manufactured for: AvKARE Pulaski, TN 38478, NDC 42291-748-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0151-2021·2020-12-23

    Taro Recalls Clotrimazole Cream Due to Unknown Impurity

    Taro Pharmaceuticals is recalling Equate Athlete's Foot cream because an unknown impurity was detected above specification limits.

    Product
    CLOTRIMAZOLE — CLOTRIMAZOLE (CLOTRIMAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0158-2021·2020-12-23

    Taro Recalls TopCare Clotrimazole Cream Due to Impurity

    Taro Pharmaceuticals is recalling TopCare Clotrimazole Cream because an unknown degradation impurity was detected slightly above the specification limit.

    Product
    TOPCARE — TOPCARE (CLOTRIMAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0615-2021·2020-12-23

    Medline Recalls RevMedX Trauma Dressings Due to Package Seal Integrity Issues

    Medline Industries is recalling RevMedX Trauma Dressings because of package seal integrity issues. The recall affects 15,780 units distributed in the US and several international countries.

    Product
    RevMedX Trauma Dressings are packaged in a Tyvek Peel pouch, 1 Trauma Dressing per Tyvec Peel Pouch, 30 Pouches per Case; Sterile - Product Usage: are intended to absorb exudates.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0164-2021·2020-12-23

    Simex Recalls Lavar 70 Gel Hand Sanitizer Due to Subpotent Drug

    Simex Logistics SA de CV is recalling Lavar 70 Gel Hand Sanitizer because it is a subpotent drug. The product was distributed in California, Georgia, Nevada, and Texas.

    Product
    Lavar 70 Gel Hand Sanitizer 70% Alcohol Content, 33.8 FL OZ (1L), Distributed By Blue Ridge Southern Supply, LLC. 1130 Aba St. Blue Ridge, GA 30513 Produced By: Simex Logistics S.A. de C.V Salvatierra No. 101 Fraccionamiento El Puente Celaya, Guanajuato, Mexico, Barcode: 7 05333
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Food)·F-0180-2021·2020-12-23

    Fusion Health Recalls Pharmorigins Core Supplement for Unapproved Additive

    Fusion Health and Vitality LLC is recalling Pharmorigins Core dietary supplements due to the unapproved use of a food additive and unapproved marketing statements.

    Product
    PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE HEALTH Dietary Supplement 30 Servings (45g) Supplement Facts***Hordenine HCL*** Manufactured by: Fusion Health Vitality, LLC 1360 Union Hill Road, Suite 11B Alpharetta, GA 30004 888.964.5327 UPC 7 28028 21054
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0157-2021·2020-12-23

    Taro Recalls Clotrimazole Cream Due to Unknown Degradation Impurity

    Taro Pharmaceuticals is recalling Best Choice Clotrimazole Cream USP 1% because an unknown degradation impurity was detected slightly above the specification limit.

    Product
    Best Choice, Clotrimazole Cream, USP 1%, Antifungal, NET WT 0.5 OZ (14.2g), Distributed by: Valu Merchandisers, CO . 5000 Kansas Ave. Kansas City, KS 66106 Made in Canada. UPC 0-70038-20355-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0177-2021·2020-12-23

    Out of the Kitchen Recalls Black Garlic Ketchup Due to Mold Risk

    Out of the Kitchen, LLC is recalling specific bottles of Chef Mitch Maier's Black Garlic Ketchup because they may develop mold before the expiration date.

    Product
    Chef Mitch Maier's Black Garlic Ketchup. Net Wt. 19 oz. (538g). UPC 8 60248-00254 5.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0155-2021·2020-12-23

    Taro Recalls Kroger Clotrimazole Cream Due to Impurity

    Taro Pharmaceuticals is recalling Kroger Clotrimazole Cream 1% because an unknown degradation impurity was detected slightly above the specification limit.

    Product
    KROGER — KROGER (CLOTRIMAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0175-2021·2020-12-23

    Black Garlic BBQ Sauce Recalled Due to Potential Mold Growth

    Out of the Kitchen, LLC is recalling specific bottles of Chef Mitch Maier's Black Garlic BBQ Sauce because they may develop mold before the expiration date.

    Product
    Chef Mitch Maier's Black Garlic BBQ Sauce. Net Wt. 19 oz. (538g). UPC 8 60248-00251 4.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0192-2021·2020-12-23

    Outshine Fruit & Cream Bars Recalled for Foreign Material Complaints

    Dreyers Grand Ice Cream is recalling Outshine Fruit & Cream Bars due to complaints of foreign material in the ice cream bars.

    Product
    Outshine Fruit & Cream Bars - Creamy Pineapple Coconut 6 fruit and dairy bars, 14.7 fl. oz. UPC: 41548 91817 4 Distributed by Nestle Dreyers Ice Cream, Oakland, CA
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0162-2021·2020-12-23

    Simex Logistics Recalls Subpotent Health & Hand Gel Hand Sanitizer

    Simex Logistics SA de CV is recalling 19,008 bottles of Health & Hand Gel Hand Sanitizer because the product is subpotent.

    Product
    Health & Hand Gel Hand Sanitizer 70% Alcohol Content, 33.8 FL OZ (1L), Distributed By Blue Ridge Southern Supply, LLC 1130 Ada St. Blue Ridge, GA 30513 Produced By: Simex Logistics S.A. de C.V. Salvatierra No. 101 Fracc. El Puente C.P. 38040 Celaya, Guanajuato, Mexico. smxcontact
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0568-2021·2020-12-23

    Galt Medical Recalls Centeze Centesis Catheters Due to Tip Geometry Defect

    Galt Medical Corporation is recalling 9,920 Centeze Centesis Catheters because a manufacturing issue resulted in incorrect tip geometry, specifically a thicker wall and more obtuse tip angle.

    Product
    Centeze Centesis Catheter, 6F, 10cm, 18Ga, 12cm, REF DRC-002-06 Centeze Centesis Catheter, 6F, 10cm, 18Ga, 12cm, REF DRC-006-16
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Drugs)·D-0160-2021·2020-12-23

    Simex Recalls Subpotent +Protec Hands Antibacterial Gel Topical Solution

    Simex Logistics SA de CV is recalling +Protec Hands Antibacterial Gel because it is subpotent. The product was distributed in California, Georgia, Nevada, and Texas.

    Product
    +Protec Hands Antibacterial Gel Topical Solution Instant Sanitizer Hands 70% Alcohol Antiseptic, packaged in bottles of a) 33.8 Oz (1000mL) Barcode: GOOD-GEL-04062020L; b) 127.8 oz (3780mL) Barcode 0723707893163, Distributed by: PS Promotional Services LLC Allen Street #406 Dalla
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-0163-2021·2020-12-23

    UVT World Gel Hand Sanitizer Recalled for Subpotent Drug Content

    Simex Logistics SA de CV is voluntarily recalling UVT World Gel Hand Sanitizer because it is a subpotent drug. The product was distributed in California, Georgia, Nevada, and Texas.

    Product
    UVT World Gel Hand Sanitizer 70% Alcohol Content, 33.9 FL OZ (1LT), Distributed By UVT World Newport Beach, CA 92660 www.uvt.world Produced By: Simex Logistics S.A. de C.V. Salvatierra No. 101 Fraccionamiento El Puente Celaya, Guanajuato, Mexico Barcode: 7 00306 88677 2
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0635-2021·2020-12-23

    Helena Laboratories Recalls K-ACT Actalyke Clotting Test Tubes

    Helena Laboratories is recalling K-ACT Actalyke Clotting Test Tubes due to complaints of cracked or split caps.

    Product
    K-ACT Actalyke Clotting Test Tubes that are used in the: ACTALYKE XL ACTIVATED CLOTTING TIME ANALYZER, and ACTALYKE MINI ACTIVATED CLOTTING TIME TEST SYSTEM.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0152-2021·2020-12-23

    Taro Recalls HEB Clotrimazole Cream Due to Impurity

    Taro Pharmaceuticals is recalling HEB Clotrimazole Cream 1% because an unknown degradation impurity was detected slightly above the specification limit.

    Product
    HEB — HEB (CLOTRIMAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0153-2021·2020-12-23

    Taro Recalls Kaiser Permanente Clotrimazole Cream Due to Impurity

    Taro Pharmaceuticals is recalling specific lots of Kaiser Permanente Clotrimazole Cream USP 1% because an unknown degradation impurity was detected slightly above the specification limit.

    Product
    Kaiser Permanente Clotrimazole Cream USP, 1% Antifungal Cream, NET WT 1 oz (28.4 g), Manufactured by Taro Pharmaceuticals Inc. Brampton, Ontario, Canada L6T1C1 Distributed by Kaiser Foundation Hospitals Livemore, CA 94551-9756. Made in Canada. NDC 0179-8014-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0612-2021·2020-12-23

    Medtronic Percept PC Neurostimulator Recall Due to Software Connection Failure

    Medtronic is recalling 12 Percept PC Implantable Neurostimulators because a software anomaly in the A620 Patient Programmer prevents connection to the device.

    Product
    Percept PC Implantable Neurostimulator (INS) - Product Usage: The Percept PC is a neurostimulation device for deep brain stimulation therapy. It is indicated for DBS treatment for Parkinson s disease, essential tremor, dystonia, obsessive-compulsive disorder, and epilepsy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0148-2021·2020-12-23

    Biogen Recalls Vumerity Capsules Due to Dissolution Test Failures

    Biogen is recalling 5,307 bottles of Vumerity capsules because they failed dissolution testing. The medication may not release the drug as intended.

    Product
    VUMERITY — VUMERITY (DIROXIMEL FUMARATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0147-2021·2020-12-23

    SCA Pharmaceuticals Recalls Fentanyl Injection Due to Low Potency

    SCA Pharmaceuticals is recalling specific lots of Fentanyl injection for IV or IM use because stability testing showed low potency.

    Product
    Fentanyl, 250 mcg/ 5mL, Injection for IV or IM use, Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct., Little Rock, AR 72205
    Category
    Drug
    Distribution
    2 states
  • SevereNHTSA·20V808000·2020-12-22

    GM Recalls 2020 Chevrolet Bolt EV for Brake Caliper Fracture Risk

    General Motors is recalling 2020 Chevrolet Bolt EV vehicles because a front left brake caliper may fracture, potentially reducing brake performance and increasing crash risk.

    Product
    CHEVROLET — CHEVROLET BOLT EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V809000·2020-12-22

    Escape Trailer Recalls 2020 RVs Due to Gas Leak Risk

    Escape Trailer is recalling 2020 RV trailers because a stove component may cause a gas leak, increasing the risk of fire.

    Product
    ESCAPE — ESCAPE ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21715·2020-12-22

    2021 Can-Am Outlander and Renegade ATVs Recalled for Rear Wheel Separation

    Bombardier Recreational Products is recalling 2021 Can-Am Outlander and Renegade ATVs because a rear wheel can separate, causing a crash hazard.

    Product
    2021 Can-Am Outlander and Renegade All-Terrain Vehicles (ATVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V802000·2020-12-21

    Mercedes-Benz and Freightliner Sprinter Vehicles Recalled for Brake Fluid Leak

    Daimler Vans USA is recalling 2019-2020 Mercedes-Benz and Freightliner Sprinter vans because rear brake calipers may leak fluid, allowing air into the hydraulic brake system.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 2500, SPRINTER 4500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V804000·2020-12-21

    Thor Motor Coach Recalls 2018-2019 Hurricane and Windsport Motorhomes

    Thor Motor Coach is recalling 2018-2019 Hurricane and Windsport motorhomes because overhead cabinets may detach and fall on occupants.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH HURRICANE, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V764000·2020-12-21

    GM Recalls 2010-2013 Buick and Chevrolet Models for Rear Suspension Defect

    General Motors is recalling specific Buick and Chevrolet vehicles because excessive corrosion protection on rear toe links may cause them to fracture, increasing crash risk.

    Product
    BUICK — BUICK, CHEVROLET LACROSSE, REGAL, MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V805000·2020-12-21

    SVI Trucks Recalls 2020 Fire Rescue Trucks Due to Display Lockup

    SVI Trucks is recalling 2020 Fire Rescue Trucks because the instrument cluster display may lock up, potentially delaying emergency efforts and increasing injury risk.

    Product
    SVI TRUCKS — SVI TRUCKS SVI TRUCKS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V807000·2020-12-21

    2021 FCCC Trucks Recalled: Brake Caliper Tie Bar Fasteners May Be Loose

    DTNA recalls certain 2021-2022 commercial trucks with potentially loose or missing brake caliper tie bar fasteners, which could affect brake function and increase crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, FCCC, THOMAS BUILT BUSES BUSINESS CLASS M2, MC, MBC, MT55
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E092000·2020-12-21

    Bendix Brake Light Switch Recall Due to Potential Jamming

    Bendix is recalling specific brake light pressure switches that may leak air, causing electrical contacts to jam and brake lights to malfunction.

    Product
    EXTERIOR LIGHTING:BRAKE LIGHTS:SWITCH recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V806000·2020-12-21

    2022 Thomas Built Buses Brake Tie Bar Installation Defect Recall

    Daimler Trucks recalls 278 model year 2022 Thomas Built SAF-T-Liner C2 school buses due to improper brake tie bar installation. The defect could increase crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V803000·2020-12-21

    Volvo Bus Recalls 2015-2020 9700 Models for Transmission Hub Failure

    Volvo Bus is recalling 2015-2020 9700 buses because a transmission hub may fail, potentially disabling the vehicle and forcing passengers to transfer on the roadside.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·029-2020·2020-12-19

    Perfect Pasta Recalls Frozen Meat and Poultry Products Lacking Federal Inspection

    Perfect Pasta Inc. is recalling frozen meat and poultry products produced without federal inspection. No adverse reactions have been reported.

    Product
    Perfect Pasta Inc. Recalls Frozen Meat and Poultry Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·030-2020·2020-12-19

    Nestlé Recalls Lean Cuisine Baked Chicken Meals Due to Plastic Contamination

    Nestlé Prepared Foods is recalling Lean Cuisine Baked Chicken meal products that may contain pieces of hard white plastic. No illnesses have been reported.

    Product
    Nestlé Prepared Foods Recalls Lean Cuisine Baked Chicken Meal Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·PHA-12192020-01·2020-12-19

    USDA Issues Public Health Alert for Ineligible Imported Frozen Chicken Wings

    USDA FSIS issued a public health alert for raw frozen chicken wings from China labeled with a false USDA mark. No recall was requested as the product is no longer in commerce.

    Product
    FSIS Issues Public Health Alert for Ineligible Imported Raw Frozen New Orleans - Roasted Chicken Wings from the Peoples Republic of China
    Category
    Food
    Distribution
    3 states
  • HighNHTSA·20V799000·2020-12-18

    2021 Forest River Puma Travel Trailers: Fire Risk from Propane Cooktop

    Forest River is recalling certain 2021 Puma travel trailers because the outdoor cooktop may be stowed with the propane hose still attached and burner on, increasing fire risk. Forest River will install a bracket to prevent the drawer from being closed while the propane line is attached.

    Product
    FOREST RIVER — FOREST RIVER PUMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V801000·2020-12-18

    2021 Keystone Cougar Recreational Trailers Recalled for Solar Wiring Defect

    Certain 2021 Keystone Cougar recreational trailers with Solar Prep wiring may have improper electrical connections that increase fire risk. Owners should contact Keystone for free inspection and remounting of the wiring.

    Product
    KEYSTONE — KEYSTONE COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V800000·2020-12-18

    Mercedes-Benz Recalls AMG GT53 and GT63 for Detaching Wheel Hub Caps

    Mercedes-Benz is recalling 2019-2020 AMG GT53 and GT63 vehicles because wheel-hub caps may detach while driving, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT63, AMG GT53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V793000·2020-12-17

    Land Rover Recalls 2020 Range Rover Evoque for Seat Belt Defect

    Jaguar Land Rover is recalling 2020 Range Rover Evoque vehicles because replacement second-row seat belts may not function properly in a crash.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V791000·2020-12-17

    Ford Recalls Transit Connect and EcoSport for Air Bag Defect

    Ford is recalling 2019-2020 Transit Connect and 2020 EcoSport vehicles because air bag modules may lack first-stage booster propellant, preventing proper deployment in a crash.

    Product
    FORD — FORD TRANSIT CONNECT, ECOSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V792000·2020-12-17

    Chevrolet Silverado 1500 Front Seat Belt Brackets May Not Secure

    General Motors is recalling certain 2020 Chevrolet Silverado 1500 and other vehicles because front-row center seat belt brackets may not be properly secured to the seat frame, potentially preventing proper restraint in a crash.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 2500, SILVERADO 3500, TAHOE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V798000·2020-12-17

    2020 Honda Insight Recalled for DC-DC Converter Power Loss Risk

    Honda is recalling certain 2020-2021 Insight, 2020 CR-V Hybrid, and 2020 Accord Hybrid vehicles due to a DC-DC converter fault that may prevent battery recharging, potentially causing loss of drive power and increasing crash risk. Owners can receive a free software update.

    Product
    HONDA — HONDA INSIGHT, ACCORD HYBRID, CR-V HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V790000·2020-12-17

    GM Recalls 2021 Cadillac Escalade for Seat Belt Light Visibility Issue

    General Motors is recalling 2021 Cadillac Escalade vehicles because the front passenger seat belt and airbag status lights may be invisible in daytime, increasing crash injury risk.

    Product
    CADILLAC — CADILLAC ESCALADE NA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V788000·2020-12-17

    2020-2021 Ford Explorer and Lincoln Aviator motor mount fastener recall

    Ford is recalling certain 2020-2021 Explorer and Lincoln Aviator vehicles because right-hand motor mount fasteners may have been incorrectly tightened and could loosen, potentially causing the axle to disconnect from the engine and loss of power.

    Product
    LINCOLN — LINCOLN, FORD AVIATOR, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V794000·2020-12-17

    Land Rover Recalls 2020 Range Rover Evoque for Seat Fire Hazard

    Land Rover is recalling 2020 Range Rover Evoque vehicles because the front seat material may burn too quickly in a fire, increasing injury risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-12172020-01·2020-12-17

    Country Meats Pork Snack Sticks Recalled for Undeclared Milk Allergen

    USDA FSIS issued a public health alert for Country Meats HOT BBQ Flavor Smoked Pork Snack Sticks due to misbranding and an undeclared milk allergen.

    Product
    Country Meats, LLC — FSIS Issues Public Health Alert for Ready-to-Eat Pork Snack Stick Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0173-2021·2020-12-16

    Hy-Vee Grill Ready Veggie Mix Recalled for Listeria

    Hy-Vee is recalling Short Cuts Grill Ready Veggie Mix because an ingredient tested positive for Listeria monocytogenes.

    Product
    Hy-Vee, Short Cuts, Grill Ready Veggie Mix sold by weight in approximate 1 lb containers, Distributed by Hy-Vee Inc, West Des Moines, IA UPC 272104 XXXXXX
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-0174-2021·2020-12-16

    Hy-Vee Pot Roast Mix Recalled for Listeria Contamination

    Hy-Vee is recalling Short Cuts Pot Roast Mix because an ingredient tested positive for Listeria monocytogenes. Consumers should discard the product.

    Product
    Hy-Vee, Short Cuts, Pot Roast Mix sold by weight in approximate 1 lb containers, Distributed by Hy-Vee Inc, West Des Moines, IA UPC 272083 XXXXXX
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0120-2021·2020-12-16

    Fresenius Kabi Recalls Dexmedetomidine Injection Due to Lidocaine Contamination

    Fresenius Kabi is recalling 13,525 bottles of Dexmedetomidine HCl Injection due to cross-contamination with trace amounts of lidocaine.

    Product
    Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg / 50 mL (4 mcg / mL), 50 mL Single Dose Bottle, Rx only, Fresenius Kabi, Lake Zurich, IL 60047, NDC 63323-671-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0179-2021·2020-12-16

    Fresh Attitude Baby Spinach Recalled for Potential Salmonella Contamination

    Veg Pro International Inc. is recalling Fresh Attitude Baby Spinach due to potential Salmonella contamination. The product was distributed across several Northeastern and Mid-Atlantic states.

    Product
    1. Fresh Attitude Baby Spinach, 11 oz. 2. Fresh Attitude Baby Spinach, 5 oz.
    Category
    Food
    Distribution
    10 states
  • SevereCPSC·21055·2020-12-16

    LG Energy Solution Recalls Home Batteries Due to Fire Hazard

    LG Energy Solution Michigan is recalling about 1,815 RESU 10H home batteries because they can overheat and cause fires. Consumers should contact the company for a free replacement.

    Product
    LG Chem "RESU 10H" Lithium-Ion Residential Energy Storage System
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V787000·2020-12-16

    2021 Thomas Built Saf-T-Liner C2 Electric School Bus Brake Recall

    Daimler Trucks North America is recalling 28 electric school buses where the parking brake may release unexpectedly, increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0121-2021·2020-12-16

    Shilpa Medicare Recalls Busulfan Injection Due to Manufacturing Deviations

    Shilpa Medicare Limited is voluntarily recalling 2,064 vials of Busulfan Injection due to CGMP deviations. The recall is nationwide and the lot expired in December 2020.

    Product
    Busulfan Injection 60 mg/10 mL (6 mg/mL), For Intravenous Infusion Only, Must be diluted before use, Single Dose Vial, Sterile, Cytotoxic Agent, Rx Only, 10 mL vial, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals, Inc., Manalapan, NJ 07726,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0126-2021·2020-12-16

    Shilpa Medicare Recalls Docetaxel Injection Due to Manufacturing Deviations

    Shilpa Medicare Limited is recalling 2,008 vials of Docetaxel Injection USP due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Docetaxel Injection USP 160 mg/8mL (20 mg/mL), For Intravenous Infusion Only, Rx Only, 8 mL Single Use Vial, Cytotoxic Agent, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals, Inc., Manalapan, NJ 07726, NDC 72485-216-08.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0117-2021·2020-12-16

    FDA Recalls Protz Antibacterial Hand Sanitizer for CGMP Violations

    Asiaticon, SA de CV is recalling 111,500 units of Protz Antibacterial Hand Sanitizer distributed in Texas due to a lack of Current Good Manufacturing Practices (CGMPs).

    Product
    Protz real protection Antibacterial Hand Sanitizer, Ethyl Alcohol 70%, 13.5 FL OZ (400 mL), Distributed by: Safety-Med Products, Inc. Burlington, WI 53105 Made in Mexico by Asiaticon S.A. de C.V. Conkal No. 62, Mexico, Ciudad de Mexico 14200, Mexico NDC: 75192-600-02 UPC 7 503019
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-0169-2021·2020-12-16

    Golden Boy Custard Muffins Recalled for Undeclared Milk and Dye

    Hong Thai Foods Corp is recalling Golden Boy Custard Muffins Original due to undeclared milk and Uranine-Acid Yellow 73.

    Product
    Golden Boy brand Custard muffin Original; 7.76 ounce, rigid clear plastic packages
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0125-2021·2020-12-16

    FDA Recalls Imatinib Mesylate Tablets Due to Manufacturing Deviations

    Shilpa Medicare Limited is recalling 4,166 bottles of Imatinib Mesylate 400 mg tablets nationwide due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    IMATINIB MESYLATE — IMATINIB MESYLATE (IMATINIB MESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V786000·2020-12-16

    Audi Recalls 2020 Q3 Vehicles Due to Brake Pedal Plate Defect

    Volkswagen Group of America is recalling 2020 Audi Q3 vehicles because the brake pedal plate can bend or detach, increasing crash risk.

    Product
    AUDI — AUDI Q3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V785000·2020-12-16

    Volkswagen Recalls 2012-2014 Beetles for Air Bag Inflator Defect

    Volkswagen is recalling 2012-2014 Beetle and Beetle Convertible vehicles because the driver's side air bag inflator may explode due to propellant degradation.

    Product
    VOLKSWAGEN — VOLKSWAGEN BEETLE CONVERTIBLE, BEETLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0168-2021·2020-12-16

    Whole Foods Market Recalls Popcorn Chicken Shaker with Sweet Chili

    Whole Foods Market is recalling Popcorn Chicken Shaker with Sweet Chili due to undeclared shrimp allergen.

    Product
    Whole Foods Market Popcorn Chicken Shaker with Sweet Chili Variable weight sold by lb. Packed For Whole Foods Market
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0161-2021·2020-12-16

    Prairie Farms Chocolate Milk Recalled for Undeclared Egg

    Prairie Farms is recalling 355 gallons of chocolate milk sold in the Chicago area due to undeclared egg.

    Product
    Prairie Farms Premium Flavored Chocolate Milk, 1 gallon, UPC 72730-26110
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0123-2021·2020-12-16

    Shilpa Medicare Recalls Azacitidine Injection Vials Due to Manufacturing Deviations

    Shilpa Medicare Limited is recalling 6,560 vials of Azacitidine for Injection due to Current Good Manufacturing Practice (CGMP) deviations. The recall is voluntary and nationwide.

    Product
    Azacitidine for Injection 100 mg/vial, For Subcutaneous and Intravenous Use Only, Rx Only, One Single Dose Vial, Cytotoxic Agent, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals, Inc., Manalapan, NJ 07726, NDC 72606-558-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0542-2021·2020-12-16

    K2M Everest MI XT Tab Removal Tool Recalled for Cracking and Leakage

    K2M, Inc. is recalling 197 units of the Everest MI XT Tab Removal Tool because the threaded interface may crack, causing Loctite to leak from the handle.

    Product
    Everest MI XT Tab Removal Tool (i.e. All-In-One Tab Removal Tool)-used to break the tab off the Everest XT screw by rocking the instrument back and forth until the entire tab is fully detached from the screw head. Catalog number: 5101-90195
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0160-2021·2020-12-16

    Prairie Farms Chocolate Milk Recalled for Undeclared Egg

    Prairie Farms is recalling 1% Lowfat Chocolate Milk due to undeclared egg. The product was sold in the Chicago area.

    Product
    Prairie Farms 1% Lowfat Chocolate Milk, 1 gallon, UPC 72730-26126
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0170-2021·2020-12-16

    Golden Boy Custard Muffin Pandan Recalled for Undeclared Milk

    Hong Thai Foods Corp is recalling Golden Boy brand Custard muffin Pandan 7.76 ounce packages because they contain undeclared milk.

    Product
    Golden Boy brand Custard muffin Pandan 7.76 ounce, rigid clear plastic packages
    Category
    Food
    Distribution
    4 states
  • HighCPSC·21054·2020-12-16

    BRP Recalls Can-Am Off-Road Screw Jacks Due to Crush Hazard

    BRP is recalling Can-Am Off-Road screw jacks because they can collapse, posing a crush hazard that could cause severe injury or death.

    Product
    Can-Am® Off-Road screw jacks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0560-2021·2020-12-16

    Medtronic Evolut PRO System Recalled for Potential Valve Leaflet Damage

    Medtronic is recalling 71,030 Evolut PRO System units worldwide due to a potential for transcatheter aortic valve leaflet damage during post-implant balloon dilatation.

    Product
    Evolut (TM) PRO System. With the following model numbers: a. EVOLUTPRO-23, Labeled as: VLV EVOLUTPRO-23 PRO COMM 29L OUS, VLV EVOLUTPRO-23 BLUE 29L COMM OUS, VLV EVOLUTPRO-23 BLUE COMM JPN, VLV EVOLUTPRO-23 BLUE 6L COMM OUS, VLV EVOLUTPRO-23 PRO COMM 29L CAN, VLV EVOLUTPRO-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0556-2021·2020-12-16

    Shimadzu MH-200S X-Ray System Recalled for Ceiling Arm Software Defect

    Shimadzu Medical Systems is recalling 22 MH-200S X-Ray systems because a software issue could cause the ceiling arm to move unexpectedly, posing a risk of collision or harm to patients and operators.

    Product
    MH-200S, system with Ceiling Suspended C-arm Support - Product Usage: intended to be used for cardiac angiography, neurovascular angiography, abdominal angiography, peripheral angiography, rotational angiography, multi-purpose angiography and whole body radiographic/fluoroscopic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0544-2021·2020-12-16

    Philips IntelliVue X2 Multi Measurement Server Speaker Failure Recall

    Philips is recalling 16 IntelliVue X2 Multi Measurement Servers because speaker failures may prevent audible alarms, potentially delaying patient treatment.

    Product
    Philips IntelliVue X2 Multi measurement Server: M3002A (865039) - Product Usage: intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates in a hospital environment and during patient transport insi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0545-2021·2020-12-16

    Philips IntelliVue MP2 Patient Monitors Recalled for Speaker Failure

    Philips is recalling two IntelliVue MP2 patient monitors because speaker failures may prevent audible alarms, potentially delaying patient treatment.

    Product
    Philips IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates in a hospital environment and during patient transport inside and outside
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0552-2021·2020-12-16

    TissueTech Recalls PROKERA Slim Corneal Bandages Due to Microbial Contamination

    TissueTech, Inc. is recalling 75 units of PROKERA Slim non-sterile biologic corneal bandages due to potential exposure to microbial contamination.

    Product
    PROKERA Slim, non-sterile - Product Usage: Biologic corneal bandage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0561-2021·2020-12-16

    Medtronic Evolut PRO+ System Recalled for Valve Leaflet Damage Risk

    Medtronic is recalling 19,961 Evolut PRO+ Transcatheter Aortic Valve systems due to a potential for leaflet damage during post-implant balloon dilatation.

    Product
    Evolut (TM) PRO+ System. With the following model numbers: a. EVPROPLUS-23US, Labeled as VLV EVPROPLUS-23US COMM JPN, VLV EVPROPLUS-23 COMM US; b. EVPROPLUS-26US, Labeled as VLV EVPROPLUS-26US COMM JPN, VLV EVPROPLUS-26 COMM US; c. EVPROPLUS-29US, Labeled as VLV E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0534-2021·2020-12-16

    Shimadzu Mobile X-Ray System Recalled for Improper Handle Bolts

    Shimadzu Medical Systems is recalling 115 Mobile X-Ray Systems because the adjustable handle may have improper bolts, posing a risk of harm to individuals around the device.

    Product
    Shimadzu Mobile X-Ray System, MobileDaRt Evolution (MX8 Version), with adjustable handle option, Made in Japan - Product Usage: The device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergen
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0167-2021·2020-12-16

    Kroger HomeChef Meal Kit Recalled Due to Suspect Listeria Ingredient

    The Kroger Co is recalling HomeChef meal kits because a pretzel breading ingredient was suspect for Listeria species, though the result was not confirmed.

    Product
    HomeChef meal kit:Steak and Walnut-Green Onion Sauce with roasted potatoes and creamed spinach.
    Category
    Food
    Distribution
    33 states
  • HighFDA (Food)·F-0162-2021·2020-12-16

    Victoria Taylor Sicilian Seasoning Recalled for Undeclared Sesame

    Victoria Gourmet is recalling 1,080 jars of Victoria Taylor Sicilian Seasoning sold in Canada because the product contains undeclared sesame.

    Product
    Victoria Taylor Seasonings Sicilian Seasoning/Assaisonement Sicilien; Italian style seasoning blend; 2.5oz; packaged in a glass jar. Canadian product only.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0540-2021·2020-12-16

    Avanos Medical Recalls Pediatric Feeding Tubes Due to Connector Detachment

    Avanos Medical is recalling 710 units of CORFLO NG/NI Pediatric Neonatal Feeding Tubes because the male AIV adaptor may detach from the Y-connector.

    Product
    CORFLO NG/NI Pediatric Neonatal Feeding Tube w/ Anti-IV Connector
    Category
    Medical Device
    Distribution
    6 states

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