The Recall Desk

Archive

September 2020 recalls

631 recalls were announced in September 2020.

What the numbers show

Critical
56
Severe
123
High
285
Moderate
154
Low
13

Of the 631 recalls this month scored against our rubric, 9% are Critical, 19% are Severe.

201–300 of 631

  • CriticalFDA (Food)·F-1430-2020·2020-09-16

    Whole Foods Market Vegan Vanilla Cake Recalled for Undeclared Soy Allergen

    Whole Foods Market is recalling 18 units of Vegan Vanilla Cake due to an undeclared soy allergen. The product was sold in parts of the Southeast.

    Product
    Whole Foods Market Vegan Vanilla Cake 6 Inch NET WT 2lb 11oz (1219g) Packed for Whole Foods Market PLU 41070 packaged in plastic dome containers with Whole Foods Market scale labels
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-1428-2020·2020-09-16

    HelloFresh and EveryPlate Meal Kits Recalled Due to Salmonella Risk

    HelloFresh US is recalling approximately 694,090 meal kits containing onions received between June 25 and July 31, 2020, due to potential Salmonella contamination.

    Product
    Various HelloFresh and EveryPlate meal kits containing onions received by consumers from June 25 through July 31, 2020.
    Category
    Food
    Distribution
    46 states
  • SevereFDA (Devices)·Z-2910-2020·2020-09-16

    CareFusion PC Unit Front Case with Keypad Replacement Kits Recalled

    CareFusion 303, Inc. is recalling PC Unit Front Case with Keypad Replacement Kits because fluid ingress may cause keys to become unresponsive or stuck, potentially delaying or interrupting life-sustaining infusions.

    Product
    PC Unit Front Case with Keypad Replacement Kits: TC10008389 ASSY CASE FRONT W/KEYPAD 8015LS, TC10010217 ASSY FRT CASE W/ KEYPAD 8015 M2, TC10012515 ASSY FR CASE W/ KEYPAD 8015 M2, TC10013702 ASSY, CASE, FRONT W/KEYPAD, 8015LS, TC10013664 ASSY FR CASE W/ KEYPAD 8015 M2
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Devices)·Z-2939-2020·2020-09-16

    CareFusion Recalls BD Alaris Infusion Pumps Due to Keypad Defects

    CareFusion is recalling BD Alaris infusion pumps because fluid ingress can cause unresponsive or stuck keys, potentially delaying or interrupting infusions.

    Product
    BD Alaris System PC Unit Model 8100 (Pump Module) and Pump Module Door Assembly Replacement Kits (P/N 49000239, 49000346, 49000438, 49000439) infusion pump.
    Category
    Medical Device
    Distribution
    54 states
  • SevereFDA (Drugs)·D-1564-2020·2020-09-16

    Just Hand Sanitizer Recalled for Methanol Labeling Error

    Open Book Extracts is recalling Just Hand Sanitizer because it was labeled to contain methanol.

    Product
    Just Hand Sanitizer (Ethyl Alcohol 73%) Single Use-Packs 100-count NDC 78065-2020-2 UPC 703123998598 (Single packs NDC 78065-2020-1 UPC 703123998659) Distributed by: Just Hand Sanitizer
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1565-2020·2020-09-16

    Shine & Clean Hand Sanitizer Recalled for Methanol and Low Ethanol

    Maquiladora Miniara S.A. de C.V. is recalling Shine & Clean Hand Sanitizer gel because FDA testing found undeclared methanol and ethanol levels below the label claim.

    Product
    Shine & Clean Hand Sanitizer gel, (Ethyl Alcohol 70%), 33.81 fl oz (1L) bottle, Made in Mexico By: Maquiladora Miniara S.A. de C.V. Carrerera Teoloyucan Huehuetoca km: 22 S/N La Planada Mexico C.P.: 54665 NDC 76753-001-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1563-2020·2020-09-16

    Open Book Extracts Recalls Hand Sanitizer Labeled With Methanol

    Open Book Extracts is recalling Always Be Clean Hand Sanitizer because it is labeled to contain methanol. The recall covers 340,000 packs distributed nationwide.

    Product
    Always Be Clean Hand Sanitizer (73% Alcohol) 0.04 FL OZ (1.2 mL) packaged in a) Single snaps (NDC 75091-2020-1 UPC 375091202016); b) 100-count boxes (NDC 75091-2020-2 UPC 375091202023); c) 25-count boxes (NDC 75091-2020-3 UPC 375091202030)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2909-2020·2020-09-16

    CareFusion Alaris System PC Unit Model 8015 Recalled for Keypad Defect

    CareFusion is recalling Alaris System PC Unit Model 8015 infusion pumps because fluid ingress can cause unresponsive or stuck keypad keys, potentially delaying or interrupting medication infusions.

    Product
    Alaris System PC Unit Model 8015
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Food)·F-1424-2020·2020-09-16

    Signature Select Granola Bars Recalled for Undeclared Peanut Butter

    Treehouse Foods is recalling Signature Select Chewy Granola Bars because they may contain undeclared peanut butter. The recall covers 1,202 cases distributed nationwide and to Saudi Arabia.

    Product
    Signature Select Chewy Granola Bars, Chocolate Chip, Family Pack, 18 bars, UPC 021130-283637. 18-0.84 oz. Net Wt 15.2 oz (432g) Distributed By Better Living Brands LLC PO Box 99, Pleasanton, CA 94566-0009,
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2882-2020·2020-09-16

    CareFusion Recalls BD Alaris Modules for Incorrect Syringe Display

    CareFusion 303, Inc. is recalling BD Alaris Syringe and PCA Modules because they may display incorrect syringe types or sizes, potentially causing infusion errors.

    Product
    BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System; Syringe/PCA Sizer Sensor Replacement Kit, P/N 122278652
    Category
    Medical Device
    Distribution
    54 states
  • HighFDA (Devices)·Z-2950-2020·2020-09-16

    Intuitive Surgical Recalls ION Reprocessing Accessories Kit Due to Catheter Failure Risk

    Intuitive Surgical is recalling 27 units of the ION Reprocessing Accessories Kit because the catheter reprocessing cover may disengage, causing chemical retention and system failure.

    Product
    ION Reprocessing Accessories Kit, IF1000 (Part Number: 490024-03) UDI:00886874119129. The kit includes an ION Catheter Reprocessing Cover (Part Number: 490114-02).
    Category
    Medical Device
    Distribution
    12 states
  • HighFDA (Food)·F-1433-2020·2020-09-16

    Arrowhead Mills Organic Yellow Popcorn Recalled for Potential Glass

    Hometown Food Company is recalling Arrowhead Mills Organic Yellow Popcorn due to the potential for glass in the finished product.

    Product
    Arrowhead Mills Organic Yellow Popcorn, 28oz bag, UPC: 0 7433347665 8, 6 retail bags per wholesale case, case item code 1 7433347665 9
    Category
    Food
    Distribution
    1 state
  • HighCPSC·20183·2020-09-16

    RH Recalls Industrial Three-Panel Mirrors Due to Injury Hazard

    RH is recalling about 270 Industrial Three-Panel Mirrors because the panels can detach and fall, posing an injury hazard. No injuries have been reported.

    Product
    Industrial Three-Panel Mirrors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1432-2020·2020-09-16

    Kader Exports Recalls Frozen Cooked Shrimp Due to Salmonella Risk

    Kader Exports is recalling 406,080 lbs of frozen cooked shrimp from multiple brands due to possible Salmonella contamination. The product was distributed nationwide.

    Product
    Cooked, Peeled and Deveined, Tail-on, Shrimp. AQUA STAR RESERVE-(1) 26/30 shrimp per pound, NET WT 1lbs UPC:3114960591 and (2) 31/40 shrimp per pound, NET WT 1lbs UPC:3114965212. CENSEA- (1) 31/40 shrimp per pound, NET WT 32Oz, 2lbs, 908g UPC:7004160011,(2) 41/50 shrimp pe
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1427-2020·2020-09-16

    Schaws Sweet With Heat Barbecue Sauce Recalled for Undeclared Allergens

    Lac O' Seasons Resort, Inc. is recalling Schaws Sweet With Heat Barbecue and Basting Sauce because it contains undeclared soy and anchovies.

    Product
    SCHAWS SWEET WITH HEAT BARBECUE AND BASTING SAUCE, 18oz glass jar, UPC code 7 93573 11599
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1437-2020·2020-09-16

    Preferred Popcorn Recalls Organic Yellow Popcorn for Foreign Material

    Preferred Popcorn is recalling organic yellow popcorn due to the potential presence of tempered glass fragments between 3 mm and 7 mm in size.

    Product
    Organic Yellow Popcorn packaged in the following ways: 1) Great Northern Organic Popcorn, Net Wt. 5 Pounds (2.26 Kilograms), UPC 6 10708 14709 1; 2) Hometown Food Company, Organic Butterfly Popcorn, 2200 LBS, Preferred Popcorn LLC Chapman, NE; 3) Lesser Evil, Organic Yel
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-1534-2020·2020-09-16

    Taylor Farms Chopped Kit Recalled for Undeclared Wheat and Sesame

    Taylor Farms is recalling BBQ Ranch Chopped Kits due to undeclared wheat and sesame allergens. The product was distributed only in Canada.

    Product
    Taylor Farms BBQ Ranch Chopped Kit Salade Coupee Chili Lime Tortilla Squares, Bacon & BBQ Ranch Dressing NET WT 277 g (13.3 oz) UPC 30223 04171
    Category
    Food
    Distribution
    0 states
  • HighNHTSA·20V560000·2020-09-16

    2020-2021 Kia Stinger fuel pump defect causing engine power loss

    Kia is recalling 2020-2021 Stinger vehicles because a fuel pump defect may block fuel flow to the engine, causing loss of power while driving and increasing crash risk.

    Product
    KIA — KIA STINGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20184·2020-09-16

    Monoprice Recalls Category 6 Ethernet Cables Due to Fire Hazard

    Monoprice is recalling Category 6 Ethernet cables that do not meet flammability standards, posing a fire hazard. Consumers should stop using the cables and contact the company for a free replacement.

    Product
    Monoprice Category 6 Ethernet Bulk CMR Communications Cables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1429-2020·2020-09-16

    Back to Nature Wheat Cracker Recall for Undeclared Milk

    B&G Foods is recalling Back to Nature Organic Rosemary and Olive Oil Stoneground Wheat Crackers because the product contains undeclared milk.

    Product
    Back to Nature, Organic Rosemary and Olive Oil Stoneground Wheat Cracker, 6 oz. foil bag inside paper carton, 6 packages per case .
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1434-2020·2020-09-16

    Southern Grove Mixed Nuts Recalled for Undeclared Brazil Nuts

    The Superior Nut Company is recalling Southern Grove Mixed Nuts because the product contains undeclared Brazil nuts, a potential allergen.

    Product
    SOUTHERN GROVE; MIXED NUTS; LESS THAN 50% PEANUTS; PEANUTS, ALMONDS, CASHEWS, HAZELNUTS, & PECANS; with Sea Salt; NET WT 14.75 OZ (418g); INGREDIENTS: PEANUTS, ALMONDS, CASHEWS, HAZELNUTS(FILBERTS), PECANS, PEANUT AND/OR COTTONSEED OIL, SEA SALT; CONTAINS: PEANUTS, TREE NUTS (ALM
    Category
    Food
    Distribution
    8 states
  • HighNHTSA·20V561000·2020-09-16

    Volkswagen Recalls 23 Internal Use Vehicles for Regulatory Compliance Issues

    Volkswagen is recalling 23 internal use vehicles, including Golf and Passat models, because they may not meet federal safety standards. Owners will be offered a repurchase.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF ALLTRACK, EGOLF, PASSAT, GOLF R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2946-2020·2020-09-16

    Smiths Medical Recalls Bivona Tracheostomy Tubes Due to Incorrect Size Labeling

    Smiths Medical ASD Inc. is recalling three Bivona Mid-Range Aire-Cuf Adult Tracheostomy Tubes because the labels display the incorrect size. The units were distributed in Connecticut.

    Product
    Bivona Mid-Range Aire-Cuf Adult Tracheostomy Tube This tube is intended to provide direct airway access for a tracheotomized patient for up to 29 days. It may be reprocessed up to 10 times for single patient use.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2938-2020·2020-09-16

    Qiagen SARS-CoV-2 Test Panel Recalled for Influenza A False Positives

    Qiagen is recalling 1,474 QIAstat-Dx Respiratory SARS-CoV-2 Panel kits due to an increased rate of false positive results for Influenza A, which may lead to inappropriate antiviral use or delayed diagnosis.

    Product
    QIAstat-Dx Respiratory SARS-CoV-2 Panel REF 691223 (US IVD under FDA EUA) - Product Usage: intended for the qualitative detection and differentiation of nucleic acid from multiple respiratory viral and bacterial organisms, including the SARS-CoV-2 virus, in nasopharyngeal swabs (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2949-2020·2020-09-16

    Intuitive Surgical Recalls Ion Catheter Reprocessing Covers

    Intuitive Surgical is recalling 67 Ion Catheter Reprocessing Covers because they may fail to engage correctly, potentially causing catheter or system failure.

    Product
    Ion Catheter Reprocessing Cover, IF1000 (Part Number:490114-02) UDI:00886874116845.
    Category
    Medical Device
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-2940-2020·2020-09-16

    Medcomp Titan HD Catheter Kits Recalled for Incorrect Valve Size

    Medical Components, Inc. is recalling 132 Medcomp Titan HD catheter kits because they were packaged with a 15F valve instead of the correct 16F valve.

    Product
    Medcomp 15.SF X 24CM Titan HD CATHETER (CUFF 19CM FROM TIP) Ref: THD155024
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-2945-2020·2020-09-16

    Smith & Nephew Recalls EVOS Screws Due to Incorrect Expiration Dates

    Smith & Nephew is recalling 71 units of EVOS Screws because the labels contain multiple or incorrect expiration dates.

    Product
    EVOS Screws - Product Usage: is a part of the EVOS MINI plating system, indicated for fracture fixation, arthrodesis, reconstruction, replantation or reduction of small bones and small bone fragments.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0013-2021·2020-09-16

    Teva Recalls Cephalexin Oral Suspension Due to CGMP Deviations

    Teva Pharmaceuticals is recalling Cephalexin for Oral Suspension because current Good Manufacturing Practice deviations may cause active ingredient levels to fall outside specification limits.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2943-2020·2020-09-16

    Talladium Luminesse Zirconia Discs Recalled for Incorrect Shrinkage Labeling

    Talladium Inc is recalling 39 Luminesse Zirconia Discs because the linear shrinkage value on the label is incorrect and outside the acceptable range.

    Product
    Talladium Luminesse Zirconia Discs, Zirconia HT Disc 98x20mm A1, Shaded Zirconia Blend 2.0 50# A1, Model No. 5147-A1;(UDI): D7915147A10 - Product Usage: are intended for CAD/CAM fabrication of all-ceramic (no metal) dental restorations. Luminesse ZR Blanks are partially sintered
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1425-2020·2020-09-16

    Culinary Collective Recalls Blanxart Chocolate Bars Due to Foreign Object

    Culinary Collective is recalling Blanxart 82% Congo Organic Chocolate Bars because a consumer found a foreign object in the product.

    Product
    Blanxart 82% Congo Organic Chocolate Bar. Paper packaging with internal foil wrapper. Net weight per bar: 4.4 oz. UPC 8 32924 00032 9. The product label is read in parts: "***BLANXART *** ORGANIC DARK CHOCOLATE 82% CONGO ***Ingredients: cocoa, cocoa butter, sugar, vanilla ***I
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1562-2020·2020-09-16

    Edge Pharma Recalls Vancomycin IV Bags Due to Labeling Error

    Edge Pharma, LLC is recalling Vancomycin HCL 1.5 mg IV bags distributed in Wisconsin due to a label error regarding the declared strength.

    Product
    Vancomycin HCL 1.5 mg Edge Pharma, LLC 856 Hercules Dr. Colchester, VT 05446 NDC 05446-1458-01
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2937-2020·2020-09-16

    Hager & Meisinger Recalls Dental Burs Due to Labeling Discrepancy

    Hager & Meisinger is recalling 144 units of SINGLES Carbide dental burs because the US dates on the package label do not match the bar code display.

    Product
    SINGLES Carbide US-No. FG556; UDI +E0HM26000313140091; STERILE R; Size 009, Length 3.8; 2025-03-18 - Product Usage: Cutting of hard structures in the mouth, such as teeth or bone, it is also intended to cut hard metals, plastics, porcelains, and similar materials intended for use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0012-2021·2020-09-16

    Teva Recalls Cephalexin Oral Suspension Due to CGMP Deviations

    Teva Pharmaceuticals is recalling specific lots of Cephalexin for Oral Suspension because current Good Manufacturing Practice deviations may cause active ingredient levels to fall outside specification limits.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1566-2020·2020-09-16

    Teva Recalls Cephalexin Oral Suspension Due to Low Potency

    Teva Pharmaceuticals is recalling Cephalexin for Oral Suspension because test results showed the drug was below the required potency specification.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2948-2020·2020-09-16

    MicroPort Recalls PROFEMUR Modular Necks for Package Insert Update

    MicroPort Orthopedics is voluntarily recalling PROFEMUR Titanium and Cobalt Chrome modular necks to replace older package inserts with the most recent revision.

    Product
    PROFEMUR Titanium and Cobalt Chrome modular necks, Item Numbers and descriptions: Item Number Description Description 2 PHAC1202 PROFEMUR NECK NEUTRAL SHORT COBALT CHROME PHAC1204 PROFEMUR NECK NEUTRAL LONG COBALT CHROME PHAC1212 PROFEMUR NECK A/R VAR/VAL 2 SHORT COBALT CHROM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V559000·2020-09-15

    Thor Motor Coach Motorhomes Tire Valve Stem Defect Recall

    Thor Motor Coach is recalling certain 2018-2021 motorhomes because the tire valve stem extension may contact the rim and become damaged, potentially causing tire pressure loss and crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TUSCANY, VENETIAN, ARIA, PALAZZO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V554000·2020-09-11

    Isuzu and Chevrolet Recall 2018-2021 Trucks for Starter Cable Fire Risk

    Isuzu and Chevrolet are recalling 2018-2021 FTR and 6500XD trucks because a broken starter ground cable could cause a fire. Owners should contact dealers for a free repair.

    Product
    ISUZU — ISUZU, CHEVROLET FTR, 6500XD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E070000·2020-09-11

    Oshkosh Recalls Bendix Pressure Switches for Brake System Air Leak Risk

    Oshkosh is recalling Bendix Pressure Switches sold as aftermarket parts because plastic threads may strip, causing air leaks that can reduce braking performance or disable brake lights.

    Product
    SERVICE BRAKES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·023-2020·2020-09-11

    Cher-Make Sausage Recalls Fully Cooked Wieners Due to Undeclared Milk

    Cher-Make Sausage Company is recalling fully cooked wieners because they contain undeclared milk (cheese). Consumers should not eat the product.

    Product
    Cher-Make Sausage Company — Cher-Make Sausage Company Recalls Fully Cooked Meat Sausage Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    6 states
  • HighCPSC·20780·2020-09-11

    Medique Recalls 31 Over-the-Counter Drugs for Non-Child-Resistant Packaging

    Medique is recalling 31 over-the-counter drugs sold on Amazon.com because the packaging is not child-resistant, posing a risk of poisoning to young children.

    Product
    31 Medique Over-the-Counter drugs from the product lines Medi-First, Medi-First Plus, Medique, Dover, Otis Clapp, and Ecolab
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·20V556000·2020-09-11

    Nissan Recalls 2019 Titan Vehicles for Headlight Aiming Mark Defect

    Nissan is recalling 2019 Titan vehicles with LED headlights because incorrect aiming marks may cause improper headlight alignment, increasing crash risk at night.

    Product
    NISSAN — NISSAN TITAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V553000·2020-09-11

    Forest River Recalls Vengeance Trailers Due to Incorrect Placard

    Forest River is recalling 2014-2016 Vengeance trailers because the Federal Placard may list an incorrect water capacity, risking overload.

    Product
    FOREST RIVER — FOREST RIVER VENGEANCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V550000·2020-09-10

    Ford Recalls 2019-2020 Vehicles for Transmission Fire Risk

    Ford is recalling 2019-2020 Edge, Transit Connect, Escape, and Lincoln models because loose bolts on the start/stop accumulator may cause a transmission fluid leak and potential fire.

    Product
    LINCOLN — LINCOLN, FORD NAUTILUS, ESCAPE, EDGE, TRANSIT CONNECT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20779·2020-09-10

    Residential Elevators Recalls Traction Elevators Due to Impact Hazard

    Residential Elevators is recalling about 6,300 traction elevators installed between 2014 and 2017 because the cab can rise unexpectedly and stop abruptly, posing an impact hazard.

    Product
    Traction elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V191000·2020-09-10

    Chrysler Recalls Jeep, Ram, and Dodge Vehicles for Rearview Camera Software Error

    Chrysler is recalling 319,610 vehicles because a software error can cause the rearview camera image to remain displayed after shifting out of reverse, increasing crash risk.

    Product
    JEEP — JEEP, CHRYSLER, RAM WRANGLER, PACIFICA, GLADIATOR, RENEGADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1386-2020·2020-09-09

    Giant Eagle Egg and Bacon Salad Recalled for Salmonella Risk

    Giant Eagle is recalling Egg & Bacon Salad With French Dressing due to potential Salmonella Newport contamination in onions.

    Product
    GE Egg & Bacon Salad With French Dressing PLU# 23665100000. Expiration date 8/4/2020. Ingredients: SALAD [ROMAINE LETTUCE, FRENCH DRESSING (SOYBEAN OIL, SUGAR, WATER, DISTILLED VINEGAR, APPLE CIDER VINEGAR, TOMATO PASTE, HONEY, CONTAINS LESS THAN 2% OF SALT, PAPRIKA, MUSTARD FLOU
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1411-2020·2020-09-09

    Giant Eagle Spinach Dip Recalled for Potential Salmonella Newport Contamination

    Giant Eagle is recalling Spinach Dip Grab & Go products due to potential contamination with Salmonella Newport in onions. Consumers in IN, OH, MD, WV, and PA should discard the product.

    Product
    SPINACH DIP GRAB & GO (INDEPENDENT PLU) PLU#25139600000. Expiration date 8/6/2020. Ingredients: SPINACH DIP [SOUR CREAM (CULTURED CREAM, ENZYME), MAYONNAISE (SOYBEAN OIL, DISTILLED VINEGAR, EGG YOLK, HIGH FRUCTOSE CORN SYRUP, CONTAINS LESS THAN 2% OF SALT, WATER, MUSTARD SEED, C
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1348-2020·2020-09-09

    Taylor Farms Recalls Chicken Salad Croissants Due to Salmonella Risk

    Taylor Farms Texas, Inc. is recalling specific chicken salad croissants due to potential Salmonella contamination. The products were distributed in Texas, Oklahoma, Kansas, and Missouri.

    Product
    Taylor Farms Retail Chicken Salad Croissant 1/6.25oz and 1/6.15oz
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1413-2020·2020-09-09

    Giant Eagle Recalls Cucumber Salad Due to Salmonella Newport Risk

    Giant Eagle is recalling Cucumber Salad (PLU#27697700000) with an expiration date of 8/3/2020 due to potential contamination with Salmonella Newport in onions.

    Product
    CUCUMBER SALAD PLU#27697700000. Expiration date 8/3/2020. Ingredients: CUCUMBER SALAD (CUCUMBER, SUGAR, WHITE VINEGAR [GRAIN, WATER], ONIONS, WATER, DILL, SALT). Onions are raw.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1347-2020·2020-09-09

    Taylor Farms Rotini Pasta Salad Recalled for Salmonella Risk

    Taylor Farms is recalling specific units of Rotini Pasta Salad due to potential Salmonella contamination. The product was distributed in Texas, Oklahoma, Kansas, and Missouri.

    Product
    Taylor Farms Retail Rotini Pasta Salad 1/10oz
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Drugs)·D-1576-2020·2020-09-09

    Mylan Recalls Tranexamic Acid Injection Due to Labeling Mix-Up

    Mylan Institutional LLC is recalling 1,407 cartons of Tranexamic Acid Injection due to a labeling error that may result in the wrong medication being dispensed.

    Product
    TRANEXAMIC ACID — TRANEXAMIC ACID (TRANEXAMIC ACID)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1421-2020·2020-09-09

    Saddlin' Up Salsa Medium Recalled for Potential Salmonella Newport Contamination

    Spokane Produce, Inc. is recalling Saddlin' Up Salsa Medium due to potential Salmonella Newport contamination from supplied onions.

    Product
    Saddlin' Up Salsa Medium, item number 83259, refrigerated product, ready to eat product, packaged in a 15 oz. plastic tub with a plastic lid. UPC 88694 83255.
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1390-2020·2020-09-09

    Giant Eagle Recalls Greek Salad With Balsamic Dressing Due to Salmonella Risk

    Giant Eagle is recalling MD Greek Salad with Balsamic Dressing due to potential Salmonella Newport contamination in onions.

    Product
    MD GREEK SALAD WITH BALSAMIC DRESSING PLU# 24660600000. Expiration date 8/4/2020, Ingredients; SALAD [ROMAINE LETTUCE, PEPPERONCINI (PEPPERS, WATER, SALT, VINEGAR, CITRIC ACID, SODIUM BENZOATE (AS PRESERVATIVE), SODIUM BISULFITE (TO ENHANCE COLOR), YELLOW 5), BALSAMIC VINAIGRETTE
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Drugs)·D-1574-2020·2020-09-09

    FDA Recalls Skin Guard 24 Hand Sanitizing Towelettes for Unapproved Methanol

    SG24 LLC is recalling Skin Guard 24 hand sanitizing towelettes because they contain unapproved methanol and lack FDA approval.

    Product
    Skin Guard 24 All-Day Hand Sanitizer 1 4"x6" Hand Sanitizing Towelette packaged in 2.5 x 3.75 packets, Dist by: SG24 LLC, Bolingbroke, GA 31004
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1570-2020·2020-09-09

    Hand Sanitizer Recalled for Methanol Contamination

    AAA Cosmetica is recalling bio aaa Advance Hand Sanitizer because it contains methanol. Consumers should stop using the product.

    Product
    bio aaa Advance Hand Sanitizer Ethyl Alcohol 70%, Unscented, 16.23 Oz (480 mL), Distributed By: Payless Janitorial Corporation 1341 SW 21 Terrance, Fort Lauderdale, Florida Exported By: E. Audicode S.A. de C.V. Manufactured By: AAA Cosmetica S.A. de C.V. UPC 7 502272 12111 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1381-2020·2020-09-09

    Giant Eagle Recalls Country Style Pasta Salad Due to Salmonella Risk

    Giant Eagle is recalling Country Style Pasta Salad with French Dressing due to potential Salmonella Newport contamination in onions.

    Product
    Country Style Pasta Salad French Dressing PLU# 22665100000. Expiration date: 8/5/2020 Ingredients: SALAD [ROMAINE LETTUCE, BUTTERMILK RANCH (SEE DRESSING CUP), GRAPE TOMATOES, BACON BITS (BACON CURED WITH: WATER, SALT, SODIUM PHOSPHATES, SODIUM ERYTHORBATE, SODIUM NITRITE, MAY C
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1346-2020·2020-09-09

    Taylor Farms Macaroni Salad Recalled for Potential Salmonella Contamination

    Taylor Farms Texas, Inc. is recalling 99 units of Retail Macaroni Salad due to potential Salmonella contamination. The product was distributed in Texas, Oklahoma, Kansas, and Missouri.

    Product
    Taylor Farms Retail Macaroni Salad 1/9.9oz
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1419-2020·2020-09-09

    Ronzoni Smart Taste Pasta Recalled for Undeclared Egg Allergen

    Riviana Foods is recalling Ronzoni Smart Taste Extra Wide Noodle Style pasta due to undeclared egg. The product was distributed in five states.

    Product
    RONZONI SINCE 1915 Smart Taste Extra Wide Noodle Style 2.5x the Fiber of Regular Pasta Net Wt. 12OZ (340g). UPC: 7130005008
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1367-2020·2020-09-09

    Giant Eagle Cucumber Tomato Salad Recalled for Salmonella Newport Risk

    Giant Eagle is recalling Cucumber Tomato Salad due to potential Salmonella Newport contamination in onions. Consumers in five states should discard the product.

    Product
    MD Salad Bar- Cucumber Tomato Salad. Expiration 07/31/2020. Ingredients:SALAD [CUCUMBER, TOMATOES, OIL BLEND (CANOLA OIL, EXTRA VIRGIN OLIVE OIL), ONIONS, VINEGAR (RED WINE VINEGAR (DILUTED WITH WATER TO 5% ACIDITY), POTASSIUM METABISULFITE (PRESERVATIVE)), DILL WEED, SALT, PEPPE
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1410-2020·2020-09-09

    Giant Eagle Recalls Spinach Dip Due to Potential Salmonella Newport Contamination

    Giant Eagle is recalling Spinach Dip Deli Service Cases due to potential contamination with Salmonella Newport in onions. The product was sold in Indiana, Ohio, Maryland, West Virginia, and Pennsylvania.

    Product
    SPINACH DIP DELI SERVICE CASE (INDEPENDENT PLU) PLU#25139500000. Expiration date 8/6/2020. Ingredients: SPINACH DIP [SOUR CREAM (CULTURED CREAM, ENZYME), MAYONNAISE (SOYBEAN OIL, DISTILLED VINEGAR, EGG YOLK, HIGH FRUCTOSE CORN SYRUP, CONTAINS LESS THAN 2% OF SALT, WATER, MUSTARD
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1343-2020·2020-09-09

    Taylor Farms Recalls Pico De Gallo Tomato Products Due to Salmonella Risk

    Taylor Farms Texas, Inc. is recalling specific Pico De Gallo tomato products due to a potential for contamination by Salmonella.

    Product
    Taylor Farms Foodservice Tomato, Pico De Gallo Pack Size 1/5#; Taylor Farms Foodservice Tomato, Pico De Gallo Tray Pack Size 2/5#; Taylor Farms Foodservice Whataburger Tomato, Pico De Gallo Pack Size 2/3.5#
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1420-2020·2020-09-09

    Saddlin' Up Salsa Hot Recalled for Potential Salmonella Newport Contamination

    Spokane Produce, Inc. is recalling Saddlin' Up Salsa Hot due to potential Salmonella Newport contamination from supplied onions.

    Product
    Saddlin' Up Salsa Hot, item number 83260, refrigerated product, ready to eat product, packaged in a 15 oz. plastic tub with a plastic lid. UPC 88694 83257.
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1400-2020·2020-09-09

    Giant Eagle Recalls Deluxe Italian Party Hoagies Due to Salmonella Risk

    Giant Eagle is recalling Deluxe Italian Party Hoagies sold in five states due to potential Salmonella Newport contamination in onions.

    Product
    DELUXE ITALIAN PARTY HOAGIE (INDEPENDENT PLU). PLU# 25085100000. Expiration date 7/31/2020. Ingredients: DELUXE ITALIAN PARTY HOAGIE [BREAD [ENRICHED WHEAT FLOUR (WHEAT FLOUR, ENZYMES, NIACIN, IRON, THIAMINE MONONITRATE, RIBOFLAVIN, FOLIC ACID), WATER, SALT, SUGAR, SOYBEAN OIL, Y
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1366-2020·2020-09-09

    Giant Eagle Recalls MD Salad Bar Red Onion Due to Salmonella Risk

    Giant Eagle is recalling MD Salad Bar Red Onion products with an expiration date of 7/31/2020 due to potential contamination with Salmonella Newport.

    Product
    MD Salad Bar-Red Onion. Expiration date 7/31/2020 Ingredients: raw red onion
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Drugs)·D-1575-2020·2020-09-09

    Mylan Recalls Amiodarone Hydrochloride Injection Due to Labeling Mix-Up

    Mylan Institutional LLC is recalling Amiodarone Hydrochloride Injection due to a labeling error where cartons may contain the wrong medication.

    Product
    AMIODARONE HYDROCHLORIDE — AMIODARONE HYDROCHLORIDE (AMIODARONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1414-2020·2020-09-09

    Giant Eagle Recalls Sandwich Toppers Platters Due to Salmonella Risk

    Giant Eagle is recalling Sandwich Toppers Platters due to potential contamination with Salmonella Newport in onions. Consumers should discard the product.

    Product
    SANDWICH TOPPERS PLATTER -UP TO 25 SANDWICHES PLU#27751700000. Expiration date 7/31/2020. Ingredients: SANDWICH TOPPERS [ICEBERG LETTUCE, PICKLES (IF BREAD & BUTTER SPEARS [CUCUMBERS, WATER, SALT, GRANULATED SUGAR, VINEGAR, NATURAL FLAVORS, SPICES, TURMERIC, 0.1% SODIUM BENZOATE
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1389-2020·2020-09-09

    Giant Eagle Recalls MD Dip-Rueben Due to Salmonella Newport Risk

    Giant Eagle is recalling MD Dip-Rueben products due to potential contamination with Salmonella Newport in onions and prepared foods containing onions.

    Product
    MD Dip-Rueben PLU# 24659500000. Expiration date 8/6/2020. Ingredients: REUBEN DIP [COOKED CORNED BEEF ROUND (CURED WITH UP TO 15% OF A SOLUTION OF: WATER, SALT, SUGAR, SODIUM PHOSPHATE, POTASSIUM LACTATE, SODIUM ERYTHORBATE, SODIUM NITRITE, SODIUM DIACETATE, GARLIC POWDER, EXTRAC
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1372-2020·2020-09-09

    Giant Eagle Recalls MD Caprese Salad Due to Salmonella Risk

    Giant Eagle is recalling MD Caprese Salad with an expiration date of 8/4/2020 due to potential Salmonella Newport contamination in onions.

    Product
    MD Caprese Salad PLU#21660900000. Expiration date 8/4/2020. Ingredients:SALAD [ROMAINE LETTUCE, MOZZARELLA CHEESE (PASTEURIZED MILK, VINEGAR, ENZYMES, SALT), GRAPE TOMATOES, BALSAMIC VINAIGRETTE (SEE DRESSING CUP), SPRING MIX (GREEN LEAVES [FRISEE, WILD ARUGULA, MACHE], RED LEAVE
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·20V548000·2020-09-09

    Jayco Recalls Motorhomes Due to Leveling System Bracket Failure Risk

    Jayco is recalling specific 2016-2019 motorhomes because leveling system brackets may fail, causing components to contact the ground and increasing crash risk.

    Product
    JAYCO — JAYCO, ENTEGRA GREYHAWK PRESTIGE, REDHAWK, GREYHAWK, redundant ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1338-2020·2020-09-09

    Taylor Farms Recalls Yellow Onions for Potential Salmonella Contamination

    Taylor Farms Texas, Inc. is recalling specific yellow onion products due to a potential for contamination by Salmonella.

    Product
    Taylor Farms Foodservice Onion Yellow Dice 1/8" Pack Size 4/5#; Taylor Farms Foodservice Onion Yellow Dice 1/4" Pack Size 4/5#; Taylor Farms Foodservice Onion Yellow Slice 1/4" Pack Size 4/5#; Taylor Farms Foodservice Onion Yellow Dice 1/4" Pack Size 2/5#; Taylor Farms Foodservi
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1369-2020·2020-09-09

    Giant Eagle Recalls Berry Feta Salad for Salmonella Newport Risk

    Giant Eagle is recalling MD Berry Feta Salad due to potential Salmonella Newport contamination in onions. Consumers should discard the product.

    Product
    MD Berry Feta Salad PLU# 20660900000. Expiration date 8/4/2020. Ingredients:SALAD [STRAWBERRIES, BABY SPINACH, FETA CHEESE ((PASTEURIZED PART-SKIM MILK, CHEESE CULTURE, SALT, ENZYMES), POWDERED CELLULOSE TO PREVENT CAKING), BALSAMIC VINAIGRETTE (SEE DRESSING CUP), CANDIED PECANS
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1357-2020·2020-09-09

    Whole Foods Market Recalls Raw Milk Cheese Due to Undeclared Egg Allergen

    Whole Foods Market is recalling Mitica La Dama Sagrada Raw Milk cheese because it contains undeclared lysozyme from egg whites.

    Product
    Whole Foods Market Mitica La Dama Sagrada Raw Milk - Aged 60 Days or More PLU 20656400000 Individual sliced cheese wrapped in plastic wrap with scale label on top.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1423-2020·2020-09-09

    Spokane Produce Recalls Salsa Verde Due to Salmonella Newport Risk

    Spokane Produce, Inc. is recalling specific Salsa Verde products due to potential contamination with Salmonella Newport. The affected items were distributed in Idaho, Montana, and Washington.

    Product
    Saddlin' Up Salsa Verde, item number 84032, refrigerated product, ready to eat product, packaged in a 15 oz plastic tub with a plastic lid. UPC 88694 84032. Salsa Verde, item number 84044, refrigerated product, ready to eat product,, packaged in a 1 gallon plastic container w
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-1572-2020·2020-09-09

    SkinGuard 24 Hand Sanitizer Recalled for Unapproved Methanol Content

    SG24 LLC is recalling SkinGuard 24 Hand Sanitizer because it is an unapproved new drug containing methanol.

    Product
    SkinGuard 24 All-Day Hand Sanitizer 8 oz. bottle with foam pump, Dist by: SG24 LLC, Bolingbroke, GA 31004 UPC 793573147125
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1472-2020·2020-09-09

    Sundial Blue Vervain Herbal Product Recalled for Unapproved Drug Claims

    Sundial Herbal Products is recalling Blue Vervain herbal products under a permanent injunction because the products are misbranded and deemed unapproved drugs.

    Product
    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***BLUE VERVAIN***1oz.***USES:FEMALE PROBLEMS, WORMS & PARASITES***"; packaged in clear plastic zip-top bags
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-1467-2020·2020-09-09

    Sundial Blood Leaf Herbal Product Recalled as Unapproved Drug

    Sundial Herbal Products is recalling Blood Leaf herbal products because they are misbranded and deemed unapproved drugs based on labeling claims.

    Product
    "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***BLOOD LEAF***1oz.***USES: SUPPLIES IRON, FOOD SUPPLEMENT***ANEMIA***"; packaged in clear plastic zip-top bags
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1571-2020·2020-09-09

    SkinGuard 24 Hand Sanitizer Recalled for Unapproved Methanol Content

    SG24 LLC is recalling SkinGuard 24 All-Day Hand Sanitizer because it is an unapproved new drug containing methanol.

    Product
    SkinGuard 24 All-Day Hand Sanitizer 2.67 oz. bottle with foam pump, Dist by: SG24 LLC, Bolingbroke, GA 31004 UPC 793573147103
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1337-2020·2020-09-09

    Triple B Corporation Recalls Charlies Produce Peeled Onions Due to Salmonella Risk

    Triple B Corporation is recalling Charlies Produce peeled onions due to potential Salmonella Newport contamination. The product was distributed in Alaska.

    Product
    Charlies Produce Anchorage, YELLOW Peeled Onions, Jumbo, Ready To Eat (RTE), keep refrigerated. Shelf-life: packing date plus 6 days. Packed in corrugated cardboard box. Net. wt. 20 lbs., no UPC. Product was peeled and packaged by Charlies Produce 9401 King St., Anchorage, AK 99
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1335-2020·2020-09-09

    Triple B Corporation Recalls Peeled Onions Due to Salmonella Newport Risk

    Triple B Corporation is recalling Charlie's Produce peeled onions due to potential Salmonella Newport contamination. The product was distributed in Alaska.

    Product
    Charlies Produce Anchorage, WHITE Peeled Onions, Jumbo, Ready To Eat (RTE), keep refrigerated. Shelf-life: packing date plus 6 days. Packed in corrugated cardboard box. Net. wt. 20 lbs., no UPC. Product was peeled and packaged by Charlie s Produce 9401 King St., Anchorage, AK 99
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·20V547000·2020-09-09

    Jayco Recalls 2019-2020 Motorhomes Due to Electrical Fire Risk

    Jayco is recalling 2019-2020 Entegra Reatta, Jayco Embark, and Entegra ReattaXL motorhomes because a damaged circuit board could increase the risk of a fire.

    Product
    ENTEGRA — ENTEGRA, JAYCO REATTA XL, REATTA, EMBARK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1373-2020·2020-09-09

    Giant Eagle Chickpea and Carrot Salad Recalled for Salmonella Risk

    Giant Eagle is recalling Chickpea & Carrot Salad Greek Dressing due to potential Salmonella Newport contamination in onions.

    Product
    Chickpea & Carrot Salad Greek Dressing PLU#21665100000. Expiration date 8/5/2020. Ingredients:SALAD [CHICKPEAS (CHICKPEAS, WATER, SALT, DISODIUM EDTA (TO PRESERVE COLOR)), VINAIGRETTE (WATER, VEGETABLE OIL [SOYBEAN AND/OR CANOLA], APPLE CIDER VINEGAR, RED WINE VINEGAR, EXTRA VIRG
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1380-2020·2020-09-09

    Giant Eagle Recalls Buffalo Chicken Salad Due to Salmonella Risk

    Giant Eagle is recalling MD Buffalo Chicken Salad due to potential Salmonella Newport contamination in onions. Consumers in IN, OH, MD, WV, and PA should not eat the product.

    Product
    MD Buffalo Chicken Salad PLU#22664600000. Expiration date: 8/4/2020 Expiration date 8/4/2020.Ingredients: SALAD [ROMAINE LETTUCE, BUTTERMILK RANCH (SEE DRESSING CUP), GRAPE TOMATOES, BACON BITS (BACON CURED WITH: WATER, SALT, SODIUM PHOSPHATES, SODIUM ERYTHORBATE, SODIUM NITRITE
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1361-2020·2020-09-09

    Whole Foods Market Recalls Sliced Cheese for Undeclared Egg Allergen

    Whole Foods Market is recalling sliced Mitica Mahon cheese nationwide due to undeclared lysozyme from egg whites, posing a risk to individuals with egg allergies.

    Product
    Whole Foods Market Mitica Mahon PLU 29341800000 Individual sliced cheese wrapped in plastic wrap with scale label on top.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E065000·2020-09-09

    Horizon Global Recalls U-Haul, Draw-Tite, and Reese Towpower Trailer Hitches

    Horizon Global is recalling specific U-Haul, Draw-Tite, and Reese Towpower trailer hitches sold between November 2019 and August 2020 due to a defect that may prevent the pintle hook from locking securely.

    Product
    TRAILER HITCHES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide

Looking for a different month? Back to 2020.