The Recall Desk

Archive

May 2021 recalls

517 recalls were announced in May 2021.

What the numbers show

Critical
40
Severe
132
High
234
Moderate
95
Low
16

Of the 517 recalls this month scored against our rubric, 8% are Critical, 26% are Severe.

Which agencies issued them

101–200 of 517

  • HighFDA (Devices)·Z-1667-2021·2021-05-26

    Bard Access Systems Recalls Groshong NXT ClearVue Catheters Due to Connector Defects

    Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.

    Product
    REF CK000516, Groshong NXT ClearVue Catheter with Sherlock 3CG Tip Positioning System (TPS) Stylet, Full Kit, 4F, Single-Lumen, TPS, CE 2797, UDI: (01)10801741107891 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0538-2021·2021-05-26

    PepsiCo Recalls Evolve Vanilla Bean Protein Shakes for Undeclared Soy

    PepsiCo is recalling Evolve Vanilla Bean Plant-Based Protein Shakes because they contain undeclared soy. The recall covers 14,830 cases distributed nationwide.

    Product
    Evolve Vanilla Bean Plant-Based Protein Shake, 11oz "Tetra Pak" carton, sold 4 cartons per retail unit. UPC on retail 4 pack: 876063007870 Packed 3 retail four packs per wholesale case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0523-2021·2021-05-26

    Newly Weds Bread Crumbs Recalled for Foreign Material

    Newly Weds Foods Inc is recalling 489 bags of bread crumbs due to the presence of foreign material. The recall covers distribution to manufacturers and distributors in 17 states and Mexico.

    Product
    Newly Weds B70731 bread crumbs X1, 25lbs bag
    Category
    Food
    Distribution
    16 states
  • HighFDA (Devices)·Z-1604-2021·2021-05-26

    Medtronic Guardian Sensor 3 Recalled for Inaccurate Readings with Hydroxyurea

    Medtronic is recalling Guardian Sensor 3 units because use with the drug hydroxyurea may cause inaccurate elevated glucose readings.

    Product
    Medtronic REF: MMT-7020LA, Guardian Sensor (3) for the following packaging: GS3 5PK US/ GTIN: 20763000336985 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose levels in persons with diabetes.
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·21141·2021-05-26

    Target Recalls Room Essentials Shower Stools Due to Fall Hazard

    Target is recalling Room Essentials Shower Stools because they can become unstable or slippery, posing a fall hazard. About 58,500 units were sold.

    Product
    Room Essentials Shower Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0507-2021·2021-05-26

    Hi Tech Pharmaceuticals Recalls Isomorph 28 Whey Protein for Undeclared Allergens

    Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate Vanilla Ice Cream dietary supplement because it contains undeclared milk, wheat, and soy.

    Product
    ISOMORPH 28 PURE WHEY iSOLATE VANILLA ICE CREAM DIETARY SUPPLEMENT NET WT. 5lb, UPC 6 49241 87837 7 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    44 states
  • HighNHTSA·21V397000·2021-05-26

    2021 KZRV SPORTTREK and STRATUS trailers water heater circuit fire hazard

    KZRV is recalling 2021 SPORTTREK and STRATUS trailers with incorrectly sized water heater circuit breakers. The wiring defect may prevent proper electrical protection and increase fire risk.

    Product
    KZRV — KZRV SPORTTREK, STRATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1613-2021·2021-05-26

    Medtronic Guardian Sensor 3 Recall for Hydroxyurea Interaction

    Medtronic is recalling Guardian Sensor 3 units because use with hydroxyurea may cause inaccurate glucose readings.

    Product
    Medtronic REF: MMT-7020D2 Guardian Sensor (3) for the following packaging: GS3 1PK 9L OUS2/ GTIN: 00763000243357 GS3 1PK 9L OUS2/ GTIN: 00763000318871 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucos
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1636-2021·2021-05-26

    Biopsybell Easynject Device Recalled for Potential Sterility Failure

    Biopsybell is recalling five Easynject vertebroplasty devices because they were labeled sterile but may not have been sterilized.

    Product
    EASYNJECT, Device for cement infusion in the vertebroplasty procedure, REF KVTGUN-DS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0504-2021·2021-05-26

    Hi Tech Pharmaceuticals Recalls Isomorph 28 Whey Protein for Undeclared Allergens

    Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate dietary supplements because FDA inspections found undeclared milk, wheat, and soy.

    Product
    ISOMORPH 28 PURE WHEY iSOLATE ORANGE CREAMSICLE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89856 6 & 5lb, UPC 6 49241 87833 9 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    44 states
  • HighNHTSA·21V394000·2021-05-26

    Pierce Recalls 2017-2021 Commercial Vehicles Due to Fuel Rail Leak Risk

    Pierce Manufacturing is recalling 2017-2021 Arrow XT, Enforcer, Impel, Quantum, Saber, and Velocity vehicles because a sealing washer defect may cause high-pressure fuel leaks, increasing fire risk.

    Product
    PIERCE — PIERCE ARROW XT, ENFORCER, VELOCITY, IMPEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1668-2021·2021-05-26

    Bard Access Systems Recalls Groshong NXT ClearVue Catheter Kits

    Bard Access Systems is recalling specific Groshong NXT ClearVue Catheter Basic Kits because the distal connector may be defective, preventing proper catheter passage or locking.

    Product
    REF 7617405, Groshong NXT ClearVue Catheter Basic Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741086998 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0493-2021·2021-05-26

    Desserts On Us Pistachio Baklava Recalled for Undeclared Milk Allergen

    Desserts On Us, Inc. is recalling 120 units of Original Pistachio Traditional Baklava because the packaging failed to declare milk as an ingredient.

    Product
    Desserts On Us Original Pistachio Traditional Baklava: Net Wt. 4 oz., (113g) UPC: 7 59098 51005 2 Desserts On Us, 57 Belle Falor Court, Arcata, CA 95521 Ingredients: Pistachios, sugar, filo dough [wheat flour(enriched with niacin, iron, thiamine mononitrate, riboflavin,
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1656-2021·2021-05-26

    Bard Access Systems Recalls Groshong NXT ClearVue Catheters Due to Connector Defects

    Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.

    Product
    REF 7655405, Groshong NXT ClearVue Catheter, Basic Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741035279 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1615-2021·2021-05-26

    Medtronic Guardian Sensor 3 Recall for Hydroxyurea Interaction

    Medtronic is recalling Guardian Sensor 3 units because use with hydroxyurea may cause inaccurate glucose readings.

    Product
    Medtronic REF: MMT-7020D4 Guardian Sensor (3) for the following packaging: GS3 1PK 2L CANADA/ GTIN: 00763000179595¿ Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose levels in persons with diabetes.
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·21V393000·2021-05-26

    Grand Design RV Travel Trailers LP Regulator Fire Risk Recall

    Grand Design is recalling 55,508 travel trailers (2016-2021 Imagine, Transcend, Momentum) for defective LP regulators that may cause excessive gas pressure and increase fire risk. Free replacement available through dealers.

    Product
    GRAND DESIGN — GRAND DESIGN IMAGINE, MOMENTUM, TRANSCEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1632-2021·2021-05-26

    Biopsybell Recalls Sterile Spine Bone Filler Due to Sterilization Concerns

    Biopsybell S.R.L. is recalling 60 units of Renova Spine Bone Filler labeled as sterile but potentially not sterilized. The product was distributed in Mississippi and Kentucky.

    Product
    RENOVA SPINE BONE FILLER 10G 12CM CENTIM. STERILE, RESFIL1112C1-US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1624-2021·2021-05-26

    Bioseal Central Line Dressing Kits Recalled for Potential Mold Growth

    Bioseal Corporation is recalling 580 Central Line Dressing Kits because the included ChloraPrep applicator may allow Aspergillus penicillioides growth, potentially breaching package integrity.

    Product
    Bioseal, Central Line Dressing Kit, containing ChloraPREP Applicator 3 mL, REF: CVC009/20, Sterile EO, Single Use Only, UDI: (01)00630094430096
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1605-2021·2021-05-26

    Medtronic Guardian Sensor 3 Recalled for Inaccurate Readings with Hydroxyurea

    Medtronic is recalling Guardian Sensor 3 units because use with the drug hydroxyurea can cause inaccurate elevated glucose readings.

    Product
    Medtronic REF: MMT-7020LB, Guardian Sensor (3) for the following packaging: GS3 1PK US/ GTIN: 763000336998 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose levels in persons with diabetes.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1666-2021·2021-05-26

    Bard Groshong NXT ClearVue Catheter Recall for Connector Defects

    Bard Access Systems is recalling specific Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.

    Product
    REF CK000379, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Full Kit, 4F, Single-Lumen, TLS, CE 2797, UDI: (01)10801741102704 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1612-2021·2021-05-26

    Medtronic Guardian Sensor 3 Recall for Hydroxyurea Interaction

    Medtronic is recalling Guardian Sensor 3 units worldwide because use with hydroxyurea may cause inaccurate high glucose readings.

    Product
    Medtronic REF: MMT-7020D1 Guardian Sensor (3) for the following packaging: GS3 1PK OUS1/ GTIN: 00643169704084 GS3 1PK 9L OUS1/ GTIN: 00763000243333 GS3 1PK 9L OUS1/ GTIN: 00763000318857 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing sy
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1655-2021·2021-05-26

    Bard Groshong Catheter Recall for Connector Defects

    Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters due to connector defects that may prevent proper catheter passage or locking.

    Product
    REF 7617408D, Groshong NXT ClearVue Catheter, Maximal Barrier Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741035262 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0494-2021·2021-05-26

    Public Goods Hair, Skin, & Nails Supplement Recalled for Undeclared Soy

    Public Goods is recalling Hair, Skin, & Nails dietary supplements because they may contain undeclared soy. Consumers with soy allergies should stop using the product.

    Product
    PUBLIC GOODS brand HAIR, SKIN, & NAILS Dietary Supplement; 60 tablets per bottle; Other ingredients: Stearic acid; croscarmellose sodium, magnesium stearate, aqueous film coating (purified water, hydroxypropyl methylcellulose, vegetable glycerin), microcrystalline cellulose.
    Category
    Food
    Distribution
    51 states
  • HighFDA (Devices)·Z-1601-2021·2021-05-26

    Medtronic Guardian Sensor 3 Recalled for Inaccurate Readings with Hydroxyurea

    Medtronic is recalling Guardian Sensor 3 units because use with the drug hydroxyurea may cause inaccurate elevated glucose readings.

    Product
    Medtronic REF: MMT-7020A, Guardian Sensor (3) for the following packaging: GS3 5PK 2L US/ GTIN: 20763000140940 GS3 5PK 2L US/ GTIN: 20763000337005 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose l
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1662-2021·2021-05-26

    Bard Access Systems Recalls Groshong NXT ClearVue Catheters Due to Connector Defects

    Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.

    Product
    REF 9617408D, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Maximal Barrier Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741036016 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1614-2021·2021-05-26

    Medtronic Guardian Sensor 3 Recalled for Inaccurate Glucose Readings

    Medtronic is recalling Guardian Sensor 3 units because use with hydroxyurea may cause inaccurate elevated glucose readings.

    Product
    Medtronic REF: MMT-7020D3 Guardian Sensor (3) for the following packaging: GS3 1 PK OUS3/ GTIN: 00643169704121 GS3 1PK 9L OUS3/ GTIN: 00763000318895 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1664-2021·2021-05-26

    Bard Access Systems Recalls Groshong NXT ClearVue Catheters Due to Connector Defects

    Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.

    Product
    REF 69655405, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Basic Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741147521 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1600-2021·2021-05-26

    Medtronic Enlite Glucose Sensor Recalled for Inaccurate Readings with Hydroxyurea

    Medtronic is recalling Enlite Glucose Sensors because use with hydroxyurea can cause inaccurate elevated readings.

    Product
    Medtronic REF: MMT-7008B, Enlite Glucose Sensor for the following packaging: ENLITE PLUS 23L 1CL / GTIN: 00643169541719 ENLITE PLUS 2L 1CL PR/ GTIN: 00643169786738 ENLITE PLUS 1PK 23L 1CL/ GTIN: 00763000421304 Product Usage: intended for use with Medtronic Diabetes (Med
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1622-2021·2021-05-26

    Bioseal Central Line Dressing Kits Recalled for Mold Contamination

    Bioseal Corporation is recalling Central Line Dressing Kits because the ChloraPrep applicator may allow Aspergillus penicillioides growth, potentially breaching package integrity.

    Product
    Bioseal, Central Line Dressing Kit, containing ChloraPREP Applicator 3 mL, REF: CVC015/20, Sterile EO, UDI: (01)00630094430157
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1599-2021·2021-05-26

    Medtronic Enlite Glucose Sensor Recall Due to Hydroxyurea Interference

    Medtronic is recalling Enlite Glucose Sensors because use with hydroxyurea may cause inaccurate elevated readings.

    Product
    Medtronic, REF: MMT-7008A, Enlite Glucose Sensor for the following packaging: ENLITE PLUS 5PK 23L 1CL /GTIN: 20643169541706, ENLT PLUS 5PK 2L 1CL PR/ GTIN: 20643169786725, ENLITE PLUS 5PK 23L 1CL/ GTIN: 20763000421292 - Product Usage: intended for use with Medtronic Diabetes (Med
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1617-2021·2021-05-26

    Medtronic Enlite Glucose Sensor Recalled for Inaccurate Readings

    Medtronic is recalling Enlite Glucose Sensors because use with hydroxyurea may cause inaccurate elevated readings.

    Product
    Medtronic, REF: MMT-7008C, Enlite Glucose Sensor for the following packaging: ENLITE AUS 1 PRESS 5PK/ GTIN: 20763000252032 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose levels in persons with diabet
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1603-2021·2021-05-26

    Medtronic Guardian Sensor 3 Recalled for Inaccurate Readings with Hydroxyurea

    Medtronic is recalling Guardian Sensor 3 units because use with hydroxyurea may cause inaccurate elevated glucose readings.

    Product
    Medtronic REF: MMT-7020GA, Guardian Sensor (3) for the following packaging: GS3 5PK US GC/ GTIN: 20763000179629 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose levels in persons with diabetes.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0537-2021·2021-05-26

    PepsiCo Recalls Evolve Protein Shakes Due to Undeclared Soy

    PepsiCo is recalling Evolve Double Chocolate Plant-Based Protein Shakes because they contain undeclared soy. The recall covers 17,381 cases distributed nationwide.

    Product
    Evolve Double Chocolate Plant-Based Protein Shake, 11oz "Tetra Pak" carton, sold 4 cartons per retail unit. UPC on retail 4 pack: 876063007887 Packed 3 retail four packs per wholesale case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0535-2021·2021-05-26

    Wolfie's Crunchy Cheddar & Jalapeno Peanuts Recalled for Undeclared Milk

    Wolfies Group Inc is recalling Crunchy Cheddar & Jalapeno Peanuts due to undeclared milk on the label. The product was distributed across all 50 states.

    Product
    Wolfie's Crunchy Cheddar & Jalapeno Peanuts Packaged in a Rice Paper Stand Up Pouch with Clear Poly Plastic Bag inside 5oz - 12 bags per case 14oz - 6 bags per case 28oz - 4 bags per case 80oz sold as individual bag
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0551-2021·2021-05-26

    Udi Gluten Free Banana Chocolate Chip Muffins Recalled for Plastic

    Conagra Brands is recalling Udi Gluten Free Banana Chocolate Chip Muffins due to the potential presence of plastic.

    Product
    Udi Gluten Free Banana Chocolate Chip Muffins, 10oz retail container of 4 muffins, 6 retail units per wholesale case. Retail unit UPC: 00-6-98997-81012-4
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0529-2021·2021-05-26

    Newly Weds Bread Crumbs Recalled for Foreign Material

    Newly Weds Foods Inc is recalling 80 bags of bread crumbs due to the presence of foreign material. The product was distributed to manufacturers and distributors in 17 U.S. states and Mexico.

    Product
    Newly Weds B72377 bread crumbs, 40lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Devices)·Z-1660-2021·2021-05-26

    Bard Access Systems Recalls Groshong NXT ClearVue Catheters Due to Connector Defects

    Bard Access Systems is recalling specific Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.

    Product
    REF 9617407, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Full Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741035996 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0495-2021·2021-05-26

    Kewpie Roasted Sesame Dressing Recalled for Pesticide Regulation Deviation

    Kewpie Roasted Sesame Dressing is being recalled because certain lots exceeded European ethylene oxide regulations.

    Product
    Kewpie Deep Roasted Sesame Dressing; 8 oz.(263ml/243g) and 64 oz. (1893 ml/1950g) bottles (glass and plastic) Refrigerate after opening. UPC 8 oz: 8 719189 240153 UPC 64 oz. 8 719189 24160 Manufactured by Q&B Foods Inc. 15547 First St., Irwindale, CA 91706
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0526-2021·2021-05-26

    Newly Weds Bread Crumbs Recalled for Foreign Material

    Newly Weds Foods Inc. is recalling 200 bags of 20lb bread crumbs due to foreign material. The voluntary recall affects distributors in 17 states and Mexico.

    Product
    Newly Weds B70819 bread crumbs, 20lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0527-2021·2021-05-26

    Newly Weds Bread Crumbs Recalled for Foreign Material

    Newly Weds Foods Inc. is recalling 1,695 bags of bread crumbs due to the presence of foreign material. The product was distributed to manufacturers and distributors in 17 U.S. states and Mexico.

    Product
    Newly Weds B70858 bread crumbs X1, 40lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Drugs)·D-0386-2021·2021-05-26

    KVK-Tech Recalls Hydrocodone and Homatropine Tablets for Impurity Failures

    KVK-Tech, Inc. is recalling 17,096 bottles of Hydrocodone Bitartrate and Homatropine Methylibromide tablets due to failed impurities and degradation specifications.

    Product
    HYDROCODONE BITARTRATE AND HOMATROPINE METHYLBROMIDE — HYDROCODONE BITARTRATE AND HOMATROPINE METHYLBROMIDE (HYDROCODONE BITARTRATE AND HOMATROPINE METHYLBROMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0389-2021·2021-05-26

    Fresenius Recalls Delflex Peritoneal Dialysis Solution Due to Labeling Error

    Fresenius Medical Care is recalling 709 cases of Delflex Peritoneal Dialysis Solution because a 4.25% dextrose bag was found inside a 1.5% dextrose box.

    Product
    DELFLEX — DELFLEX (DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0518-2021·2021-05-26

    Newly Weds Breader X1 Recalled for Foreign Material Contamination

    Newly Weds Foods Inc is recalling 506 bags of Breader X1 due to foreign material contamination. The product was distributed to manufacturers and distributors in 17 US states and Mexico.

    Product
    Newly Weds B54288 breader X1, 40lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Devices)·Z-1593-2021·2021-05-26

    Gore Viabil Biliary Endoprosthesis Recalled for Length Discrepancy

    W.L. Gore & Associates is recalling 61 Gore Viabil Biliary Endoprosthesis devices because a complaint reported a device appeared shorter than its labeled length.

    Product
    GORE VIBIL Biliary Endoprosthesis: stents, drains and dilators for the biliary ducts. Catalogue numbers: VH1008040, VH1010040, VN1010040, VN0808200 - Product Usage: intended for palliation of malignant strictures in the biliary tree.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1659-2021·2021-05-26

    Bard Groshong NXT ClearVue Catheter Recalled for Connector Defects

    Bard Access Systems is recalling specific Groshong NXT ClearVue catheters due to defects in the distal connector that may prevent proper catheter passage or locking.

    Product
    REF 9617405, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Basic Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741035989 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·021-2021·2021-05-26

    Legacy Food Company Recalls Beef Jerky for Undeclared Sesame Oil

    Legacy Food Company is recalling beef jerky products because they contain sesame oil, which is not listed on the label.

    Product
    Legacy Food Company Inc, — Legacy Food Company, Inc. Recalls Beef Jerky Products Due to Misbranding and an Undeclared Ingredient
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1621-2021·2021-05-26

    Boston Scientific Recalls ELUVIA Drug-Eluting Vascular Stent System Due to Packaging Error

    Boston Scientific is recalling 27 units of the ELUVIA Drug-Eluting Vascular Stent System because some 6x40mm stents were incorrectly placed in 6x100mm packaging.

    Product
    ELUVIA Drug-Eluting Vascular Stent System - Product Usage: indicated for improving luminal diameter in the treatment of symptomatic de-novo or restenotic lesions in the native superficial femoral artery (SFA) and/or proximal popliteal artery with reference vessel diameters (RVD)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0514-2021·2021-05-26

    Newly Weds Bread Crumbs Recalled for Foreign Material

    Newly Weds Foods Inc is recalling 125 bags of 40lb bread crumbs due to foreign material. The voluntary recall covers distributors in 17 US states and Mexico.

    Product
    Newly Weds A70178 bread crumbs X1, 40lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0522-2021·2021-05-26

    Newly Weds Bread Crumbs Recalled for Foreign Material

    Newly Weds Foods Inc is recalling 850 bags of bread crumbs due to the presence of foreign material. The product was distributed to manufacturers and distributors in 17 states and Mexico.

    Product
    Newly Weds B70722 bread crumbs X1, 35lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Drugs)·D-0391-2021·2021-05-26

    Sun Pharma Recalls CEQUA Eye Drops for Subpotency and Particulates

    Sun Pharmaceutical Industries is recalling CEQUA (cyclosporine) ophthalmic solution due to subpotent drug levels and the presence of particulates.

    Product
    CEQUA — CEQUA (CYCLOSPORINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0533-2021·2021-05-26

    Newly Weds Pecan Crusted Mix Recalled for Foreign Material

    Newly Weds Foods is recalling Pecan Crusted Mix due to potential foreign material contamination. The voluntary recall affects 121 units distributed across 17 states and Mexico.

    Product
    Newly Weds G52587 PECAN CRUSTED MIX X1, 4, 3lbs bag per unit
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0543-2021·2021-05-26

    21st Century Vitamin D3 Tablets Recalled for Incorrect Labeling

    Twenty-First Century Healthcare is recalling 21st Century Vitamin D3 tablets because some bottles were mislabeled with a lower dosage.

    Product
    21st Century Vitamin D3 125 mcg (5000 IU) tablet, 100 count, UPC 7-40985-27431-6, 21st Century HealthCare, Inc., 2119 Wilson St., Tempe, AZ 85282
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-0512-2021·2021-05-26

    NOW Health Group Recalls Acidophilus Capsules Due to Foreign Material

    NOW Health Group is recalling 10,235 bottles of NOW 4x6 Acidophilus because foreign capsules were found in the product.

    Product
    NOW 4x6 Acidophilus, 60 capsules per retail bottle. Item number 2920. UPC 7 33739 02920 1
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0532-2021·2021-05-26

    Newly Weds Bread Crumb Recalled for Foreign Material

    Newly Weds Foods Inc is recalling 28 bags of bread crumb due to foreign material. The product was distributed to manufacturers and distributors in 17 states and Mexico.

    Product
    Newly Weds B7AAM9 bread crumb, 40lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0528-2021·2021-05-26

    Newly Weds Bread Crumbs Recalled for Foreign Material

    Newly Weds Foods Inc. is recalling 50-pound bags of bread crumbs due to the presence of foreign material. The recall covers 3,592 bags distributed to manufacturers and distributors in 17 U.S. states and Mexico.

    Product
    Newly Weds B70971 bread crumbs X1, 50lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0513-2021·2021-05-26

    Newly Weds Bread Crumbs Recalled for Foreign Material

    Newly Weds Foods Inc is recalling 59 bags of bread crumbs due to the presence of foreign material. The product was distributed to manufacturers and distributors in 17 states and Mexico.

    Product
    Newly Weds A70088 bread crumbs X1, 35lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0515-2021·2021-05-26

    Newly Weds Breader X1 Recalled for Foreign Material Contamination

    Newly Weds Foods Inc is recalling 302 bags of Breader X1 due to foreign material. The product was distributed to manufacturers and distributors in 17 states and Mexico.

    Product
    Newly Weds B50509 breader X1, 40lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0519-2021·2021-05-26

    Newly Weds Breader X2 Recalled for Foreign Material

    Newly Weds Foods Inc is recalling 250 bags of Breader X2 due to the presence of foreign material. The product was distributed to manufacturers and distributors in 17 states and Mexico.

    Product
    Newly Weds B55713 breader X2, 50lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0550-2021·2021-05-26

    Faribault Foods Recalls O Organics Organic Chili Beans Due to Seal Defect

    Faribault Foods is recalling O Organics Organic Chili Beans because the cans have compromised hermetic seals. Consumers should stop using the product.

    Product
    O Organics Organic Chili Beans, 15 oz. can, UPC 0-79893- 40617-6 Distributed by Lucerne Foods, Inc. P.O. Box 99, Pleasanton, CA 94566-0009, 1-800-232-4271
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-0520-2021·2021-05-26

    Newly Weds Breader X1 Recalled for Foreign Material

    Newly Weds Foods Inc is recalling 250 bags of Breader X1 due to foreign material. The product was distributed to manufacturers and distributors in 17 states and Mexico.

    Product
    Newly Weds B58915 breader X1, 40lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0530-2021·2021-05-26

    Newly Weds American Bread Crumbs Recalled for Foreign Material

    Newly Weds Foods Inc is recalling 50 bags of American bread crumbs due to the presence of foreign material. The recall covers distributors in 17 states and Mexico.

    Product
    Newly Weds B74002 American bread crumbs, 35lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0554-2021·2021-05-26

    Udi Gluten Free Double Chocolate Muffins Recalled for Plastic

    Conagra Brands is recalling Udi Gluten Free Double Chocolate Muffins due to the potential presence of plastic.

    Product
    Udi Gluten Free Double Chocolate Muffins, 10oz (284g) retail container of 4 muffins, 6 retail units per wholesale case. Retail unit UPC: 00-6-98997-81039-1 (domestic) 00-6-98997-81043-8 (Canada)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0534-2021·2021-05-26

    Newly Weds Stuffed Crab Seasoning Recalled for Foreign Material

    Newly Weds Foods Inc is recalling 43 bags of Stuffed Crab Seasoning due to the presence of foreign material. The product was distributed to manufacturers and distributors in 17 U.S. states and Mexico.

    Product
    Newly Weds G94866 Stuffed Crab Seasoning X1, 34.45lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0521-2021·2021-05-26

    Newly Weds Breader Crumbs Recalled for Foreign Material

    Newly Weds Foods Inc. is recalling 142 bags of B70709 breader crumbs due to the presence of foreign material. The product was distributed to manufacturers and distributors in 17 states and Mexico.

    Product
    Newly Weds B70709 breader crumbs X3, 40lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0525-2021·2021-05-26

    Newly Weds Bread Crumbs Recalled for Foreign Material

    Newly Weds Foods Inc. is recalling 44 bags of bread crumbs due to the presence of foreign material. The product was distributed to manufacturers and distributors in 17 states and Mexico.

    Product
    Newly Weds B70814 bread crumbs X1, 40lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0548-2021·2021-05-26

    Faribault Foods Recalls S&W Organic Black Beans Due to Compromised Seals

    Faribault Foods is recalling S&W Organic Black Beans because some cans have compromised hermetic seals. Consumers should check their cans and return them for a refund.

    Product
    S&W Organic Black Beans, 15 oz. can, Distributed by: Faribault Foods, 3401 Park Ave NW, Faribault, MN 55021.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-0516-2021·2021-05-26

    Newly Weds Breader Recalled for Foreign Material

    Newly Weds Foods Inc is recalling 250 bags of Breader X1 due to the presence of foreign material. The product was distributed to manufacturers and distributors in 17 states and Mexico.

    Product
    Newly Weds B52792 breader X1, 35lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0524-2021·2021-05-26

    Newly Weds Bread Crumbs Recalled for Foreign Material Contamination

    Newly Weds Foods Inc. is recalling 726 bags of bread crumbs due to the presence of foreign material. The product was distributed to manufacturers and distributors in 17 states and Mexico.

    Product
    Newly Weds B70787 bread crumbs X2, 40lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0517-2021·2021-05-26

    Newly Weds Breader X1 Recalled for Foreign Material

    Newly Weds Foods Inc. is recalling 124 bags of Breader X1 due to the presence of foreign material. The product was distributed to manufacturers and distributors in 17 U.S. states and Mexico.

    Product
    Newly Weds B53339 breader X1, 40lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0531-2021·2021-05-26

    Newly Weds Bread Crumbs Recalled for Foreign Material

    Newly Weds Foods Inc is recalling 1,000 bags of 35lb bread crumbs due to foreign material. The voluntary recall affects distributors in 17 U.S. states and Mexico.

    Product
    Newly Weds B7AAJ5 bread crumbs X1, 35lbs bag
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Food)·F-0553-2021·2021-05-26

    Udi Gluten Free Blueberry Muffins Recalled for Potential Plastic Presence

    Conagra Brands is recalling Udi Gluten Free Blueberry Muffins due to the potential presence of plastic. Consumers should check lot codes and stop eating the product.

    Product
    Udi Gluten Free Blueberry Muffins, 10oz (284g) retail container of 4 muffins, 6 retail units per wholesale case. Retail unit UPC: 00-6-98997-81038-4 (domestic) 00-6-98997-81044-5 (Canada)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0387-2021·2021-05-26

    Nomax Recalls Subpotent Dry Eye Test Fluorescein Sodium Strips

    Nomax Inc. is voluntarily recalling 78 cartons of Dry Eye Test strips due to subpotent drug content. The FDA classified this as a Class III recall.

    Product
    DRY EYE TEST — DRY EYE TEST (FLUORESCEIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0540-2021·2021-05-26

    Lopez Gonzalez Santana Recalls BTREX PLUS Dietary Supplement Due to Damaged Tablets

    Lopez Gonzalez Santana Corporation is recalling BTREX PLUS dietary supplement caplets due to the presence of damaged tablets, a Current Good Manufacturing Practice (CGMP) deviation.

    Product
    BTREX PLUS, Dietary Supplement 2 Caplets, UPC 05380930802 (Physician Samples)
    Category
    Drug
    Distribution
    0 states
  • SevereNHTSA·21V384000·2021-05-25

    Life Line Recalls 2019-2020 RAM 5500 Vehicles for Brake Line Defect

    Life Line Emergency Vehicles is recalling 2019-2020 RAM 5500 vehicles because improperly routed rear brake lines may chafe and leak fluid, increasing crash risk.

    Product
    LIFELINE — LIFELINE RAM 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V385000·2021-05-25

    Van Hool Recalls 681 Buses Due to Fuel Rail Leak Risk

    Van Hool is recalling 681 buses because a sealing washer may not seat correctly, allowing the high-pressure fuel rail to leak and increasing fire risk.

    Product
    VAN HOOL — VAN HOOL CX45, CX35, TX45, TDX25
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V386000·2021-05-25

    Seagrave Fire Apparatus Recalls 2017-2020 Models Due to Fuel Leak Risk

    Seagrave is recalling 2017-2020 Marauder, Attacker, and Capitol vehicles because a sealing washer defect may cause high-pressure fuel leaks, increasing fire risk.

    Product
    SEAGRAVE — SEAGRAVE MARAUDER, ATTACKER, CAPITAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-05242021·2021-05-25

    USDA Issues Alert for Frozen Cooked Diced Chicken Due to Listeria

    USDA FSIS issued a public health alert for approximately 130,860 pounds of frozen, fully cooked diced chicken products due to possible Listeria monocytogenes contamination.

    Product
    FSIS Issues Public Health Alert for Frozen, Cooked Diced Poultry Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·21V387000·2021-05-25

    2020 Tesla Model 3 brake caliper bolts may loosen and separate

    Tesla is recalling certain 2020 Model 3 vehicles because brake caliper bolts may loosen, causing the caliper to separate and lose tire pressure, increasing crash risk.

    Product
    TESLA — TESLA MODEL 3, MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V390000·2021-05-25

    2021 Ford F-Series trucks recalled for improper front wheel hub attachment

    Ford is recalling 17,616 of its 2021 F-Series trucks with dual rear wheels and front wheel hub extenders. The hub extenders may be improperly attached, risking wheel separation and crash.

    Product
    FORD — FORD F-450 SD, F-550 SD, F-350 SD, F-600 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V389000·2021-05-25

    Tesla Recalls Model 3 and Model Y for Seat Belt Fastener Defect

    Tesla is recalling 2018-2020 Model 3 and 2019-2021 Model Y vehicles because front seat belt fasteners may not be properly attached, increasing injury risk.

    Product
    TESLA — TESLA MODEL Y, MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V379000·2021-05-24

    2021 Ford F-350 and F-450 Cracked Fifth Wheel Mounting Bracket Recall

    Ford is recalling certain 2021 F-350 SD and F-450 SD vehicles with fifth wheel left-hand mounting brackets that may be cracked. A cracked bracket could result in the fifth wheel detaching during towing, increasing crash risk.

    Product
    FORD — FORD F-450 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V381000·2021-05-24

    Ford Recalls 2021 F-150 Trucks Due to Driveshaft Assembly Defect

    Ford is recalling 2021 F-150 vehicles because improperly assembled driveshafts may separate, potentially causing loss of drive power or unintended movement.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V383000·2021-05-24

    Great Dane Recalls 2022 Champion Trailers Due to Brake Bolt Issue

    Great Dane is recalling 2022 Champion trailers because brake caliper bolts may loosen, reducing brake effectiveness and increasing crash risk.

    Product
    GREAT DANE — GREAT DANE CHAMPION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V382000·2021-05-24

    Honda Motorcycles Recalled for Defective Rear Reflectors

    Honda is recalling certain 2020-2021 motorcycles because the rear reflector lens may not reflect brightly enough. This defect reduces visibility and increases the risk of crashes or injuries.

    Product
    HONDA — HONDA CBR500R, CB500X, C125, CB650R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V380000·2021-05-24

    Keystone Cougar Travel Trailer Frame Rails Recalled for Buckling Risk

    Keystone is recalling 2017-2021 Cougar travel trailers because the frame rails lack sufficient cross support and can buckle under side-load stress. Buckled frames can increase crash risk.

    Product
    KEYSTONE — KEYSTONE COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V377000·2021-05-24

    2021 Ford Edge vehicles recalled for defective seatbelt retractors

    Ford is recalling certain 2021 Edge vehicles for a defective driver's seatbelt retractor pretensioner assembly that may fail to function during a crash. A faulty seatbelt increases injury risk in accidents.

    Product
    FORD — FORD EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V378000·2021-05-24

    2021 Forest River Sierra and Sandpiper trailers recalled for loose chassis bolts

    Forest River is recalling certain 2021 Sierra and Sandpiper trailers whose chassis bolts were improperly tightened. The trailers could detach from their chassis, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER SANDPIPER, SIERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V376000·2021-05-24

    Ford Transit Connect 2013-2021 shifter cable bushing defect recall

    Ford is recalling 2013-2021 Transit Connect vehicles with 2.5L engines (approximately 192,080 units) because the shifter cable bushing may degrade or detach, preventing proper gear selection and causing unexpected vehicle movement or rollaway, increasing crash and injury risk.

    Product
    FORD — FORD TRANSIT CONNECT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·020-2021·2021-05-22

    Otten's Seafood Recalls Catfish Products Produced Without Federal Inspection

    Otten's Seafood Inc. is recalling approximately 46,804 pounds of fresh and frozen catfish products because they were produced without the benefit of federal inspection.

    Product
    Otten's Seafood Inc. Recalls Siluriformes Fish Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    2 states
  • SevereUSDA FSIS·019-2021·2021-05-21

    Milan Provisions Recalls Jalapeno Chorizo Sausage Produced Without Federal Inspection

    Milan Provisions Co. Inc. is recalling approximately 6,000 pounds of jalapeno chorizo sausage because it was made with pork ingredients produced without the benefit of federal inspection.

    Product
    Milan Provision Co., Inc. — Milan Provisions Co. Inc. Recalls Jalapeno Chorizo Sausage Products Formulated With Pork Ingredients Produced Without the Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·21E047000·2021-05-21

    Lippert Recalls Hehr 6400 Series RV Windows Due to Adhesive Failure

    Lippert is recalling Hehr 6400 Series windows for recreational vehicles because the adhesive may fail, causing the vent to detach and increasing crash risk.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V375000·2021-05-21

    Rugged Mountain Custom RV K2 Recalled for Gas Leak Risk

    Tiny Idahomes is recalling 2019 Rugged Mountain Custom RV K2 trailers because a stove component may cause a continuous gas leak, increasing fire risk.

    Product
    RUGGED MOUNTAIN CUSTOM RV — RUGGED MOUNTAIN CUSTOM RV K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V374000·2021-05-21

    2021 Forest River Columbus Trailer Brakes May Fail Due to Wiring Defect

    Forest River is recalling 2021 Columbus Fifth Wheel trailers due to an incorrectly wired breakaway switch that may prevent the trailer brakes from activating, increasing the risk of crashes.

    Product
    FOREST RIVER — FOREST RIVER COLUMBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V372000·2021-05-20

    Newmar Motorhomes Recalled for Fuel Rail Seal Defect and Fire Risk

    Newmar is recalling 1,294 motorhomes from 2017-2022 due to a defective fuel rail sealing washer that could cause fuel leaks and increase fire risk. Dealers will inspect and replace the affected rails at no cost.

    Product
    NEWMAR — NEWMAR MOUNTAIN AIRE, DUTCH STAR, VENTANA, NEW AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V371000·2021-05-20

    2021 Forest River Columbus Dining Chair Legs May Detach During Use

    The Allure Swivel Dining chair legs in 2021 Forest River Columbus trailers may detach, creating an injury risk if occupied. Dealers will install reinforcing hardware free of charge.

    Product
    FOREST RIVER — FOREST RIVER COLUMBUS
    Category
    Consumer Product
    Distribution
    Distributed nationwide

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