The Recall Desk

Archive

March 2022 recalls

662 recalls were announced in March 2022.

What the numbers show

Critical
25
Severe
167
High
312
Moderate
150
Low
8

Of the 662 recalls this month scored against our rubric, 4% are Critical, 25% are Severe.

501–600 of 662

  • HighNHTSA·22V128000·2022-03-04

    Hino Recalls 2022 NJ7A Trucks Due to Air Brake Fastener Issue

    Hino is recalling 2022 NJ7A vehicles because an improperly tightened air compressor nut may cause low air pressure, potentially triggering the parking brake and increasing crash risk.

    Product
    HINO — HINO NJ7A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V127000·2022-03-04

    2022 Kia Sorento Vehicles Recalled for Seatbelt Pretensioner Defect

    Kia is recalling 2022 Sorento Hybrid and Sorento PHEV vehicles because the front seatbelt pretensioner(s) may explode during a crash, potentially projecting metal fragments at occupants. Dealers will replace the pretensioners at no cost.

    Product
    KIA — KIA SORENTO HYBRID, SORENTO PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V121000·2022-03-03

    Motorhome tire valve stem may lose pressure, increasing crash risk

    Jayco and Entegra motorhomes from 2018–2023 may have defective tire valve stem extensions that contact the wheel rim, causing damage and potential tire pressure loss that increases crash risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO ACCOLADE, ACCOLADE XL, SENECA PRESTIGE, SENECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E016000·2022-03-03

    Pony.ai Recalls Automated Driving Systems Due to Software Shutdown Risk

    Pony.ai is recalling specific Automated Driving Systems (ADS) because a software error may cause the system to shut down unexpectedly while the vehicle is moving.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V123000·2022-03-03

    2022 Hyundai Elantra and Elantra HEV Seat Belt Pretensioner Explosion Hazard

    Hyundai is recalling 2022 Elantra and Elantra HEV vehicles because the front passenger-side seat belt pretensioner may explode during a crash, projecting metal fragments that could strike and injure vehicle occupants.

    Product
    HYUNDAI — HYUNDAI ELANTRA, ELANTRA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22732·2022-03-03

    Ski-Doo Snowmobiles Recalled Due to Fire Hazard

    About 700 Ski-Doo snowmobiles from 2020–2022 are recalled because fuel can leak from the tank vent onto hot components when tilted or flipped, posing a fire hazard. BRP has received five reports of fires but no injuries.

    Product
    Ski-Doo Snowmobiles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V122000·2022-03-03

    Kawasaki Recalls W800 Motorcycles Due to Horn Harness Defect

    Kawasaki is recalling 2019-2022 W800 motorcycles because the horn harness may break, rendering the horn inoperable and increasing crash risk.

    Product
    KAWASAKI — KAWASAKI W800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0780-2022·2022-03-02

    Kroger veggie blend recalled for Listeria contamination from harvest equipment

    Dole Fresh Vegetables Inc is recalling Kroger 12 oz Veggie Blend after harvest equipment tested positive for Listeria monocytogenes. The affected products have codes beginning with W and best-by dates from December 22, 2021 through January 9, 2022.

    Product
    Kroger 12 oz Veggie Blend UPC: 0-11110-91048-6 SKU: 3013
    Category
    Food
    Distribution
    37 states
  • CriticalFDA (Food)·F-0748-2022·2022-03-02

    Dole Shredded Lettuce Recalled for Listeria Contamination Risk

    Dole recalled shredded lettuce after harvest equipment tested positive for Listeria monocytogenes. Affected products with 'B' codes and best-by dates of December 23, 2021–January 8, 2022 were distributed in the US and Canada.

    Product
    Dole 16oz Value Size Shredded Lettuce UPC:0-71430-84616-2 SKU: 157
    Category
    Food
    Distribution
    37 states
  • CriticalFDA (Food)·F-0796-2022·2022-03-02

    President's Choice Southwest Salad Kit Recalled for Listeria Risk

    Dole Fresh Vegetables Inc is recalling Presidents Choice Southwest Salad Kit due to potential Listeria monocytogenes contamination from harvest equipment used to collect raw iceberg lettuce for the product.

    Product
    Presidents Choice 13 oz. Southwest Salad Kit / Le Choix du President Sud-Ouest UPC: 0-60383-02319-5 SKU 3282
    Category
    Food
    Distribution
    37 states
  • CriticalFDA (Food)·F-0752-2022·2022-03-02

    Dole Peppercorn Ranch Chopped Kit Recalled for Listeria Contamination

    Dole Fresh Vegetables Inc is recalling the 9.1oz Peppercorn Ranch Chopped Kit due to potential Listeria monocytogenes contamination detected in harvest equipment. Affected products were distributed across the United States and Canada with best-by dates between December 23, 2021 and January 8, 2022.

    Product
    Dole 9.1oz Peppercorn Ranch Chopped Kit UPC: 0-71430-00093-9 SKU: 728
    Category
    Food
    Distribution
    37 states
  • CriticalFDA (Food)·F-0742-2022·2022-03-02

    Dole Very Veggie Lettuce Recalled for Listeria in Harvest Equipment

    Dole is recalling 10oz Very Veggie lettuce after Listeria monocytogenes was detected in harvest equipment. Affected products have best-by dates from December 23, 2021 through January 8, 2022.

    Product
    Dole 10oz Very Veggie UPC: 0-71430-01008-2 SKU: 532
    Category
    Food
    Distribution
    37 states
  • CriticalFDA (Food)·F-0794-2022·2022-03-02

    Presidents Choice Ranch Kit Recalled for Listeria in Harvest Equipment

    Dole Fresh Vegetables is recalling Presidents Choice 12.25 oz Ranch Kits due to Listeria monocytogenes detected in harvest equipment used for raw iceberg lettuce. Affected products have codes beginning with W and best-by dates of December 22, 2021 through January 9, 2022.

    Product
    Presidents Choice 12.25 oz Ranch Kit / Le Choix du President Ranch Kit de Salade UPC: 0-60383-00493-4 SKU 3614
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0790-2022·2022-03-02

    Marketside Shredded Lettuce Recalled Due to Listeria Contamination

    Dole Fresh Vegetables Inc is recalling Marketside 16 oz Shredded Lettuce due to Listeria monocytogenes found in harvest equipment. Affected products have code markings beginning with W and best-by dates from December 22, 2021 through January 9, 2022.

    Product
    Marketside 16 oz Shredded Lettuce UPC: 6-81131-53209-9 SKU: 3118
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0763-2022·2022-03-02

    President's Choice Garden Salad Recalled for Listeria Risk

    Dole Fresh Vegetables is recalling President's Choice 12oz Garden Salad due to potential Listeria monocytogenes contamination detected in harvest equipment. Affected products have best-by dates from December 23, 2021 through January 8, 2022.

    Product
    President's Choice 12oz Garden Salad / Le Choix du President Salade Jardiniere UPC:0-60383-22268-0 SKU: 3234
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0793-2022·2022-03-02

    Mixed greens recall linked to Listeria monocytogenes in harvest equipment

    Dole Fresh Vegetables is recalling Presidents Choice 12 oz Mixed Greens due to Listeria monocytogenes found in harvest equipment. The recall affects 578,243 cases distributed across Canada and the United States.

    Product
    Presidents Choice 12 oz Mixed Greens / Le Choix du President Melange de Legumes-Feuilles UPC: 0-60383-00188-9 SKU 3236
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0760-2022·2022-03-02

    Marketside Classic Salad Recalled for Listeria in Harvest Equipment

    Dole Fresh Vegetables is recalling Marketside 24oz Classic Salad due to Listeria monocytogenes contamination found in harvest equipment. The recall affects approximately 578,243 cases distributed across the U.S. and Canada.

    Product
    Marketside 24oz Classic Salad UPC:6-81131-32895-1 SKU: 3193
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0786-2022·2022-03-02

    Dole Little Salad Bar Shredded Lettuce Recalled for Listeria monocytogenes

    Dole Fresh Vegetables is recalling Little Salad Bar 8 oz Shredded Lettuce because harvest equipment was found to contain Listeria monocytogenes. Affected products have best-by dates from December 22, 2021 through January 9, 2022.

    Product
    Little Salad Bar 8 oz Shredded Lettuce UPC: 4099100087963 SKU: 3404
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0771-2022·2022-03-02

    Dole Southwest Salad Kit Recalled Due to Listeria Contamination Risk

    Dole Fresh Vegetables Inc is recalling its 13 oz Southwest Salad Kits due to Listeria monocytogenes detected in harvest equipment. Consumers should not consume affected products with best-by dates December 22, 2021 through January 9, 2022.

    Product
    Dole 13 oz Southwest Salad Kit UPC: 0-71430-01701-2 SKU: 2776
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0795-2022·2022-03-02

    Presidents Choice Sesame Ginger Kit Recalled for Listeria Contamination

    Dole Fresh Vegetables is recalling Presidents Choice Sesame Ginger Kit salad kits due to Listeria monocytogenes found in harvest equipment. Approximately 578,243 cases were distributed across the US and Canada.

    Product
    Presidents Choice 13 oz. Sesame Ginger Kit¿/ Le Choix du President Sesame et Gingembre UPC: 0-60383-02320-1 SKU 3283
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0746-2022·2022-03-02

    Dole Country Ranch Lettuce Kit Recalled for Potential Listeria Contamination

    Dole Fresh Vegetables Inc is recalling Dole 13.25oz Country Ranch Kits after Listeria monocytogenes was detected in harvest equipment. Products have best-by dates from December 23, 2021 through January 8, 2022.

    Product
    Dole 13.25oz Country Ranch Kit UPC:0-71430-01730-2 SKU: 761
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0797-2022·2022-03-02

    Dunkin Caramel Swirl recalled for undeclared milk allergen from mislabeling

    Lyons Magnus is recalling 1900 cases of Dunkin Caramel Swirl because individual containers are incorrectly labeled as Mocha Swirl without allergen warnings but contain milk.

    Product
    Dunkin Caramel Swirl: 6x 64 fl. oz. per case. Product number 4862 UPC case: 10045796048628 Ingredients: Sweetened condensed nonfat milk, high fructose corn syrup, sugar water, brown sugar, caramel color, natural flavors, potassium sorbate (a Preservative), salt. Allergens:
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0755-2022·2022-03-02

    HEB 8oz Shredded Lettuce Recalled Due to Listeria Contamination

    HEB 8oz Shredded Lettuce is being recalled due to Listeria monocytogenes found in harvest equipment. The recall affects approximately 578,243 cases distributed across Canada and multiple U.S. states.

    Product
    HEB 8oz Shredded Lettuce UPC: 0-41220-35521-1 SKU: 3308
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0779-2022·2022-03-02

    Dole Fresh Vegetables Recalls Kroger Salad Mix for Listeria

    Dole Fresh Vegetables recalled Kroger 12 oz Classic Garden salad mix after Listeria monocytogenes was found in harvest equipment. Affected products have codes beginning with W and best-by dates from December 22, 2021 through January 9, 2022.

    Product
    Kroger 12 oz Classic Garden UPC: 0-11110-91036-3 SKU: 3007
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0747-2022·2022-03-02

    Dole Southwest Salad Kit Recalled for Listeria Risk

    Dole Fresh Vegetables has recalled Dole 13oz Southwest Kit salads after Listeria monocytogenes was detected in harvest equipment used for raw lettuce. The affected product was distributed across the US and Canada.

    Product
    Dole 13oz Southwest Kit UPC:0-71430-01701-2 SKU: 2776
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0778-2022·2022-03-02

    Kroger American Blend Lettuce Recalled for Listeria Contamination Risk

    Dole Fresh Vegetables recalls Kroger American Blend lettuce due to Listeria found on harvest equipment. Affected products distributed across the US and Canada have best-by dates from December 22, 2021 to January 9, 2022.

    Product
    Kroger 12 oz American Blend UPC: 0-11110-91041-7 SKU: 3003
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0782-2022·2022-03-02

    Kroger shredded iceberg lettuce recalled due to Listeria contamination

    Dole Fresh Vegetables is recalling Kroger brand shredded iceberg lettuce due to Listeria monocytogenes found in harvest equipment. Affected products have codes beginning with W and best-by dates December 22, 2021 through January 9, 2022.

    Product
    Kroger 8oz. Shredded Iceberg Lettuce UPC: 0-11110-91613-6 SKU: 3029
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0792-2022·2022-03-02

    Presidents Choice Garden Salad recalled due to Listeria contamination risk

    Presidents Choice 12 oz Garden Salad is being recalled due to Listeria monocytogenes detected in harvest equipment. Products with codes beginning with W and best-by dates December 22, 2021 through January 9, 2022 are affected.

    Product
    Presidents Choice 12 oz Garden Salad / Le Choix du President Salade Jardiniere UPC: 0-60383-22268-0 SKU: 3234
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0765-2022·2022-03-02

    President's Choice Southwest Salad Kit recalled for Listeria contamination

    Dole Fresh Vegetables is recalling President's Choice Southwest Salad Kit due to Listeria monocytogenes on harvest equipment. The 578,243 cases distributed across the United States and Canada have best-by dates from December 23, 2021, through January 8, 2022.

    Product
    President's Choice 13oz Southwest Salad Kit / Le Choix du President Sud-Ouest UPC:0-60383-02319-5 SKU: 3282
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0745-2022·2022-03-02

    Dole Garden Salad recalled for Listeria contamination in harvest equipment

    Dole 12oz Garden Salad / Salade Du Jardin is recalled due to Listeria monocytogenes contamination detected in harvest equipment used for raw iceberg lettuce. Affected products have code dates between December 23, 2021 and January 8, 2022.

    Product
    Dole 12oz Garden Salad / Salade Du Jardin UPC:0-71430-01135-5 SKU: 2673
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0788-2022·2022-03-02

    Dole Recalls Marketside Iceberg Salad Due to Listeria Contamination

    Dole Fresh Vegetables is recalling Marketside 12 oz Classic Iceberg Salad due to Listeria monocytogenes detected in harvest equipment. Consumers should not eat the affected product and should discard or return it.

    Product
    Marketside 12 oz Classic Iceberg Salad UPC: 6-81131-32894-4 SKU: 3107
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0759-2022·2022-03-02

    Marketside Shredded Lettuce Recalled for Listeria Contamination

    Dole Fresh Vegetables Inc is recalling Marketside 1lb Shredded Lettuce due to potential Listeria monocytogenes contamination found on harvest equipment. The affected products have codes beginning with "B" and best-by dates from December 23, 2021 through January 8, 2022.

    Product
    Marketside 1lb Shredded Lettuce UPC: 6-81131-53209-9 SKU: 3118
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0785-2022·2022-03-02

    Little Salad Bar Garden Salad recalled for Listeria in harvest equipment

    Dole Fresh Vegetables Inc is recalling Little Salad Bar 12 oz Garden Salad because harvest equipment used in production tested positive for Listeria monocytogenes. Approximately 578,243 cases were distributed to Ohio and California, with broader distribution across multiple U.S. states and Canadian provinces.

    Product
    Little Salad Bar 12 oz Garden Salad UPC: 4099100082982 SKU: 3210
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0774-2022·2022-03-02

    Dole Shredded Lettuce Recalled Due to Listeria monocytogenes in Harvest Equipment

    Dole Fresh Vegetables Inc is recalling Dole Shredded Lettuce because harvest equipment was found to contain Listeria monocytogenes. This is an FDA Class I recall.

    Product
    Dole 16 oz Shredded Lettuce UPC: 0-71430-84616-2 SKU: 157 2029 Dole 8 oz Shredded Lettuce UPC: 0-71430-01065-5 SKU 2029
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0761-2022·2022-03-02

    Marketside Shredded Lettuce recalled due to Listeria in harvest equipment

    Dole is recalling Marketside 8oz Shredded Lettuce due to Listeria monocytogenes found in harvest equipment. The recall affects 578,243 cases distributed across Canada and the United States.

    Product
    Marketside 8oz Shredded Lettuce UPC: 6-81131-32896-8 SKU: 3129
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0770-2022·2022-03-02

    Dole Asian Island Crunch salad recalled for Listeria monocytogenes

    Dole Fresh Vegetables Inc is recalling Dole 13 oz Asian Island Crunch salad due to Listeria monocytogenes detected in harvest equipment. Products were distributed across multiple US states and Canadian provinces.

    Product
    Dole 13 oz Asian Island Crunch / Croustillante Des Iles Asiatiques UPC: 0-71430-01721-0 SKU: 930
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0787-2022·2022-03-02

    Dole Fresh Vegetables recalls Italian salad due to Listeria in harvest equipment

    Dole Fresh Vegetables is recalling Little Salad Bar 9 oz Italian Salad because harvest equipment was found to contain Listeria monocytogenes. The product was widely distributed to multiple U.S. states and Canadian provinces.

    Product
    Little Salad Bar 9 oz Italian Salad UPC: 4099100083194 SKU: 3215
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0789-2022·2022-03-02

    Dole Marketside Crisp Greens Recalled for Listeria Contamination

    Dole Fresh Vegetables Inc recalls Marketside 12 oz Crisp Greens after harvest equipment tested positive for Listeria monocytogenes. The product was distributed in the United States and Canada with best-by dates between December 22, 2021 and January 9, 2022.

    Product
    Marketside 12 oz Crisp Greens UPC: 6-81131-35503-2 SKU: 3265
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0791-2022·2022-03-02

    Marketside 24 oz Classic Iceberg Salad Recalled for Listeria Contamination

    Dole Fresh Vegetables is recalling Marketside 24 oz Classic Iceberg Salad due to Listeria monocytogenes found on harvest equipment used to prepare the product. Distribution included all US states and parts of Canada.

    Product
    Marketside 24 oz Classic Iceberg Salad UPC: 6-81131-32895-1 SKU: 3193
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0751-2022·2022-03-02

    Dole Shredded Lettuce Recalled Due to Listeria Monocytogenes Contamination

    Dole Fresh Vegetables Inc is recalling 8oz packages of shredded lettuce because harvest equipment was found to contain Listeria monocytogenes. The recalled products have best-by dates from December 23, 2021 through January 8, 2022.

    Product
    Dole 8oz Shredded Lettuce UPC: 0-71430-01065-5 SKU: 2029
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0743-2022·2022-03-02

    Dole Iceberg Lettuce Recalled Due to Listeria Contamination

    Dole 11oz Greener Selection iceberg lettuce is being recalled due to Listeria monocytogenes found in harvest equipment. Approximately 578,243 cases were distributed across multiple US states and Canadian provinces.

    Product
    Dole 11oz Greener Selection UPC: 0-71430-01008-2 SKU: 34
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0758-2022·2022-03-02

    Marketside Crisp Greens Recalled Due to Listeria in Harvest Equipment

    Dole Fresh Vegetables Inc. recalled Marketside 12oz Crisp Greens due to Listeria monocytogenes found in harvest equipment. Over 578,000 cases were distributed across the U.S. and Canada.

    Product
    Marketside 12oz Crisp Greens UPC: 6-81131-35503-2 SKU: 3265
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0768-2022·2022-03-02

    Dole Iceberg Lettuce Recalled Due to Listeria in Harvest Equipment

    Dole Fresh Vegetables Inc is recalling Dole brand 12 oz iceberg lettuce (UPC 0-71430-00933-8) because harvest equipment tested positive for Listeria monocytogenes. Approximately 578,243 cases were distributed across the US and Canada.

    Product
    Dole 12 oz American / Melange Americain UPC: 0-71430-00933-8 SKU: 687
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0754-2022·2022-03-02

    HEB American Salad recalled due to Listeria monocytogenes contamination

    HEB 12oz American Salad produced by Dole Fresh Vegetables is being recalled because Listeria monocytogenes was found in harvest equipment. The recall affects products with best-by dates from December 23, 2021 through January 8, 2022.

    Product
    HEB 12oz American Salad UPC: 0-41220-35500-6 SKU: 3301
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0781-2022·2022-03-02

    Dole recalls Kroger 24 oz lettuce salad due to Listeria

    Dole Fresh Vegetables is recalling Kroger 24 oz Classic Garden lettuce salad because harvest equipment was found contaminated with Listeria monocytogenes. Consumers should not eat the affected product.

    Product
    Kroger 24 oz Classic Garden UPC: 0-11110-91037-0 SKU: 3009
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0783-2022·2022-03-02

    Little Salad Bar Caesar Salad Kit Recalled for Listeria Contamination

    Dole Fresh Vegetables is recalling Little Salad Bar Caesar Salad Kit due to Listeria monocytogenes detected in harvest equipment used for raw iceberg lettuce. Approximately 578,243 cases were distributed to multiple US states and Canadian provinces.

    Product
    Little Salad Bar 10 oz Caesar Salad Kit UPC: 4099100 087000 SKU: 3214
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0776-2022·2022-03-02

    Dole Peppercorn Ranch Chopped Kit Recalled Due to Listeria in Harvest Equipment

    Dole Fresh Vegetables recalls 9.1 oz Peppercorn Ranch Chopped Kits due to Listeria monocytogenes found in harvest equipment. The affected products were distributed across Canada and the United States.

    Product
    Dole 9.1 oz Peppercorn Ranch Chopped Kit UPC: 0-71430-00093-9 SKU: 728
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0749-2022·2022-03-02

    Dole Garden Salad recalled due to Listeria contamination

    Dole Fresh Vegetables is recalling Dole 24oz Value Size Garden Salad due to Listeria monocytogenes contamination found in harvest equipment. Best-by dates December 23, 2021 through January 8, 2022 are affected.

    Product
    Dole 24oz Value Size Garden Salad UPC:0-71430-01136-2 SKU: 2109
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0775-2022·2022-03-02

    Dole 9.1 oz Peppercorn Ranch Salad Recalled for Listeria Contamination

    Dole Fresh Vegetables Inc is recalling its 9.1 oz Peppercorn Ranch salad for Listeria monocytogenes contamination found in harvest equipment. Consumers should not consume affected packages.

    Product
    Dole 9.1 oz Peppercorn Ranch / Ranch et Poivre UPC: 0-71430-00098-4 SKU: 1011
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0766-2022·2022-03-02

    Dole Very Veggie salad recalled for Listeria contamination in harvest equipment

    Dole Fresh Vegetables Inc is recalling 10 oz Very Veggie salad mix due to Listeria monocytogenes found in harvest equipment. The affected product codes begin with W with best-by dates December 22, 2021–January 9, 2022.

    Product
    Dole 10 oz Very Veggie / Ranache de Legumes UPC: 0-71430-01008-2 SKU: 2684
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0750-2022·2022-03-02

    Dole Garden Salad Recalled for Listeria Contamination on Harvest Equipment

    Dole recalled 3-pound garden salads after harvest equipment tested positive for Listeria monocytogenes. Affected product codes begin with B, with best-by dates December 23, 2021–January 8, 2022.

    Product
    Dole 3lb Garden Salad UPC:0-71430-01138-6 SKU: 2163
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0767-2022·2022-03-02

    Dole Iceberg Lettuce Recalled for Listeria in Harvest Equipment

    Dole Fresh Vegetables recalled iceberg lettuce (Greener Selection, 11 oz) due to Listeria monocytogenes detected in harvest equipment. The recall affects 578,243 cases distributed across Canada and the United States.

    Product
    Dole 11 oz Greener Selection / Selection de Verdure UPC: 0-71430-00965-9 SKU: 695
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0764-2022·2022-03-02

    President's Choice Sesame Ginger Kit Recalled for Listeria Contamination Risk

    Dole Fresh Vegetables is recalling President's Choice 13oz Sesame Ginger Kit due to Listeria monocytogenes detected in harvest equipment. Approximately 578,243 cases distributed across Canada and the United States are affected.

    Product
    President's Choice 13oz Sesame Ginger Kit / Le Choix du President Sesame et Gingembre UPC:0-60383-02320-1 SKU: 3283
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0744-2022·2022-03-02

    Dole Iceberg Lettuce Recalled Due to Listeria Contamination

    Dole Fresh Vegetables is recalling 12oz iceberg lettuce packages because harvest equipment was found to contain Listeria monocytogenes.

    Product
    Dole 12oz American UPC:0-71430-00933-8 SKU: 43
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0773-2022·2022-03-02

    Dole salad kits recalled for Listeria contamination in harvest equipment

    Dole is recalling Country Ranch Kit salads because harvest equipment used to prepare the product was found to contain Listeria monocytogenes. Consumers should not eat affected products.

    Product
    Dole 13.25 Country Ranch Kit UPC: 0-71430-01730-2 SKU: 761
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0753-2022·2022-03-02

    Dole Chopped Teriyaki Pineapple Kit Recalled for Listeria Contamination

    Dole Fresh Vegetables Inc is recalling its 9.8oz Chopped Teriyaki Pineapple Kit due to Listeria monocytogenes detected in harvest equipment used for raw iceberg lettuce. The product was distributed across multiple U.S. states and Canadian provinces.

    Product
    Dole 9.8oz Chopped Teriyaki Pineapple Kit UPC:0-71430-00100-4 SKU: 791
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0769-2022·2022-03-02

    Dole Garden Salad Recalled Due to Listeria Contamination in Harvest Equipment

    Dole Fresh Vegetables Inc is recalling multiple sizes of Dole Garden Salad due to Listeria monocytogenes found in harvest equipment used during lettuce harvesting.

    Product
    Dole 12 oz Garden Salad / Salade du Jardin UPC: 0-71430-01135-5 SKU: 2673 Dole 2 lb Garden Salad UPC: 0-71430-01137-9 SKU 2504 Dole 24 oz Value Size Garden Salad UPC: 0-71430-01136-2 SKU 2109
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0802-2022·2022-03-02

    Weis Original Potato Salad recalled for undeclared milk allergen

    Garden-Fresh Foods, Inc. is voluntarily recalling Weis Original Potato Salad due to undeclared milk. The product was distributed in six states; consumers with milk allergies should not consume affected packages.

    Product
    Weis Original Potato Salad, Net Wt 64 oz (4 lb) 1.81kg. UPC 41497-19347. Keep Refrigerated
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0756-2022·2022-03-02

    HEB Premium Ranch Kit recalled for potential Listeria contamination

    Dole Fresh Vegetables is recalling HEB 9.5oz Premium Ranch Kit due to potential Listeria monocytogenes contamination in harvest equipment used for the lettuce.

    Product
    HEB 9.5oz Premium Ranch Kit UPC: 0-41220791569-0 SKU: 3349
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0762-2022·2022-03-02

    Presidents Choice Ranch Kit recalled for potential Listeria contamination

    Dole Fresh Vegetables is recalling Presidents Choice 12.25oz Ranch Kit because Listeria monocytogenes was detected in harvest equipment used for the lettuce.

    Product
    Presidents Choice 12.25oz Ranch Kit / Le Choix du President Ranch Kit de Salade UPC: 0-60383-00493-4 SKU: 3614
    Category
    Food
    Distribution
    37 states
  • SevereNHTSA·22V118000·2022-03-02

    Freightliner M2 Brake Drum Defect May Cause Loss of Brake Function

    Daimler Trucks is recalling certain 2020-2022 Freightliner M2 trucks due to brake drum cracking that can cause brake failure and increase crash risk. All vehicles have been remedied.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V119000·2022-03-02

    BMW Recalls Multiple Models Due to PCV Valve Fire Risk

    BMW is recalling specific 2006-2013 models because a short circuit in the PCV valve heater could cause a fire while driving or when parked.

    Product
    BMW — BMW Z4, 3 SERIES, X5 SAV, X3 SAV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0645-2022·2022-03-02

    RISE UP RED EDITION Capsules recalled for undeclared tadalafil

    RISE UP RED EDITION Capsules, 650 mg, have been recalled because they contain undeclared tadalafil, an ingredient found in FDA-approved male sexual enhancement products. The product is an unapproved drug and was distributed nationwide via Amazon Marketplace.

    Product
    RISE UP RED EDITION Capsules, 650 mg, 10-count blisters packaged in a carton, ASIN B08JCWG84D, barcode X002NI8PE1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·22089·2022-03-02

    Fitbit Recalls Ionic Smartwatches Due to Burn Hazard

    Fitbit is recalling about 1 million Ionic smartwatches sold in the U.S. because the lithium-ion battery can overheat and cause burns. At least 115 reports of battery overheating have been received, including 78 burn injuries.

    Product
    Fitbit Ionic smartwatches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0757-2022·2022-03-02

    Marketside 12oz Classic Salad Recalled for Listeria Contamination

    Dole Fresh Vegetables is recalling Marketside 12oz Classic Salad due to Listeria monocytogenes found on harvest equipment used for raw iceberg lettuce. Affected products have best-by dates between December 23, 2021 and January 8, 2022.

    Product
    Marketside 12oz Classic Salad UPC:6-81131-32894-4 SKU: 3107
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0777-2022·2022-03-02

    Dole Teriyaki Pineapple Kit recalled for Listeria contamination

    Dole is recalling certain Teriyaki Pineapple Kits due to Listeria monocytogenes detected in harvest equipment. Affected products have codes beginning with W and best-by dates from December 22, 2021 through January 9, 2022.

    Product
    Dole 9.8 oz Chopped Teriyaki Pineapple Kit UPC: 0-71430-00100-4 SKU: 791 Dole 9.8 oz Chopped Teriyaki Pineapple Kit / Teriyaki A L'ananas UPC: ¿0-71430-00182-0 SKU 1014
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0772-2022·2022-03-02

    Dole Southwest Salad Kit recalled for Listeria contamination in harvest equipment

    Dole Fresh Vegetables Inc recalled its 13 oz Southwest Salad Kit after Listeria monocytogenes was detected in harvest equipment used for the raw iceberg lettuce. The company is asking consumers not to consume the product.

    Product
    Dole 13 oz Southwest Salad Kit / Salade du Sud-ouest UPC: 0-71430-01711-1 SKU: 2976
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0784-2022·2022-03-02

    Little Salad Bar Caesar Kit Recalled for Listeria in Harvest Equipment

    Dole Fresh Vegetables Inc is recalling Little Salad Bar 10.65 oz. Chopped Caesar Kit (UPC: 4099100263923) because Listeria monocytogenes was found on harvest equipment. The product was distributed across 578,243 cases in the US and Canada.

    Product
    Little Salad Bar 10.65 oz. Chopped Caesar Kit UPC: 4099100263923 SKU: 3411
    Category
    Food
    Distribution
    37 states
  • HighFDA (Devices)·Z-0669-2022·2022-03-02

    RESODURA Matrix Onlay Recalled Due to Unsealed Packaging

    Collagen Matrix is recalling RESODURA matrix onlay dural substitutes due to outer packaging that is not properly sealed, potentially compromising sterility and creating a risk of infection.

    Product
    RESODURA matrix onlay 10.0 cm x 12.5 cm - indicated as dural substitutes for the repair of dura matter. REF: DUMO10125
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22090·2022-03-02

    ALDI Bee Happy Advent Calendars Recalled for Excessive Lead Paint

    ALDI is recalling Bee Happy 12 Days of Craft Advent Calendars due to lead paint on a brown bell in Day 10 that exceeds the federal lead paint ban. The product poses a risk of lead poisoning if the paint is ingested, particularly for young children.

    Product
    Bee Happy 12 Days of Craft Advent Calendars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22091·2022-03-02

    Petzl PIRANA Descender Canyoneering Devices Recalled for Drowning Risk

    Petzl is recalling about 3,450 PIRANA descender canyoneering devices because the rope can get caught in the blocking slot, stopping or suspending the climber and creating a drowning risk under waterfalls or pools.

    Product
    PIRANA descender canyoneering devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0666-2022·2022-03-02

    Bard SureStep Intermittent Catheter Tray recalled for potential leak defect

    C.R. Bard is recalling 2,120 units of the BARD SURESTEP INTERMITTENT CATHETER TRAY (14Fr) due to a potential leak at the catheter-to-drain-bag connection.

    Product
    BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0665-2022·2022-03-02

    BD Vacutainer Luer Lok Access Device may shed particles causing false test results

    BD's Vacutainer Luer Lok Access Device may release contaminant particles that can be misidentified as red blood cells in laboratory analysis, potentially leading to false elevated RBC counts.

    Product
    BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a catheter port equipped with a threaded female luer during blood or urine sample collection using evacuated BD Vacutainer Blood or Urine Collection Tubes Catalog
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0741-2022·2022-03-02

    Arillis Tortillas Recalled Due to Undeclared Wheat Allergen

    Arillis Corp is recalling Tortillas Arillis due to undeclared wheat. Consumers with wheat allergies may be at risk if they consume the product.

    Product
    Tortillas Arillis, Arillis Corp, Contains: 10 (ten) tortillas
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0672-2022·2022-03-02

    Biomet Shoulder Implant Stem Recalled for Inadequate Coating Adhesion

    Biomet is recalling a Comprehensive Shoulder System implant component due to a defect in the porous plasma coating. The coating may not have sufficient adhesion strength, compromising the implant's structural integrity.

    Product
    Comprehensive Shoulder System Primary Shoulder Stem, Micro Length, Porous Plasma, 14 MM, 55 MM Long Item Number: 113614
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0667-2022·2022-03-02

    Bard Surestep Intermittent Catheter Tray Recalled for Connection Leaks

    C.R. Bard Inc recalled 1,620 units of Bard Surestep Intermittent Catheter Tray because the catheter may leak where it connects to the drain bag. No injuries have been reported.

    Product
    BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS16C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0801-2022·2022-03-02

    Diastatic Malt Powder Recalled Due to Potential Salmonella Contamination

    Malt Products Corporation is recalling approximately 3,015 bags of Diastatic Malt Powder due to potential Salmonella contamination. The affected product was distributed to multiple states; consumers should not consume it.

    Product
    Diastatic Malt Powder 50lb bag - up to 50 bags per pallet Malt Products Corporation
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-0661-2022·2022-03-02

    Video Camera Ceiling Tile Kits May Fall in Some Installations

    Natus Neurology is recalling IPELA FHD PTZ tile kits that may not fit properly in thinner ceiling tile grids and could suddenly fall, creating a safety hazard.

    Product
    IPELA FHD PTZ TILE KITS with Axis cameras used in combination with Natus Neuroworks/Sleepworks software
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0660-2022·2022-03-02

    Optima Coil System Recalled for Labeling and Packaging Mix-Up

    BALT USA recalls Optima Coil System embolization devices due to labeling/pouch mix-up that could result in incorrect device selection during surgical procedures. Potential harms include vessel damage and aneurysm rupture.

    Product
    The Optima Coil System consists of an implantable embolization coil comprised of a platinum-tungsten alloy attached to a proximal stainless steel hypo-tube and distal body coil delivery pusher with a radiopaque distal positioning marker and proximal fluorosafe marker. The Optima
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0657-2022·2022-03-02

    Medtronic Endurant Stent Graft Systems: Taper Tip Detachment Risk

    Certain Medtronic Endurant stent graft systems may have taper tips that detach from the delivery system during implant procedures, potentially requiring secondary surgical intervention.

    Product
    Endurant, Endurant II and Endurant IIs Stent Graft System: Medtronic Endurant Stent Graft System Model/REF ENBF2313C120EE; ENBF2313C120EE; ENBF2313C145EE; ENBF2313C170EE; ENBF2316C120EE; ENBF2316C145EE; ENBF2316C170EE; ENBF2513C120EE; ENBF2513C145EE; ENBF2513C170EE;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0671-2022·2022-03-02

    Shoulder Implant Stem Coating Defect Due to Invalid Rework Process

    Biomet is recalling a shoulder implant stem due to a manufacturing defect in the porous plasma coating. Internal testing indicated the coating may not have sufficient adhesion strength after an unvalidated waterjet rework process.

    Product
    Comprehensive Shoulder System Primary Shoulder Stem, Micro Length, Porous Plasma, 11 MM, 55 MM Long Item Number: 113611
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0670-2022·2022-03-02

    Hip implant revision system recalled due to inadequate coating adhesion

    Biomet is recalling 19 units of the Arcos Modular Revision Hip System because an incorrect rework process may have weakened the coating's adhesion strength, posing a potential implant failure risk.

    Product
    Arcos Modular Revision Hip System, Standard Cone Prox Body, Porous Plasma,Size A, 60 MM Item Number: 11-301301
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0676-2022·2022-03-02

    Biomet Shoulder Implant Stem Recalled for Coating Adhesion Defect

    Biomet recalls 9 Comprehensive Shoulder System Mini Humeral Stems due to potential coating adhesion defects. An incorrect rework process may have compromised the porous plasma coating adhesion strength.

    Product
    Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 13 MM, 83 MM Long Item Number: 113633
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0658-2022·2022-03-02

    NobelReplace dental implant components recalled for driver engagement defect

    Nobel Biocare is recalling 702 NobelReplace dental implant components due to a manufacturing defect that prevents proper driver engagement. The defect could result in aborted or delayed surgical procedures.

    Product
    NobelReplace Conical Connection RP 4.3x11.5 mm REF 36707 STERILE R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0668-2022·2022-03-02

    Collagen Dura Substitute Membrane Recalled for Compromised Sterility

    Collagen Matrix is recalling 68 units of DuraMatrix-Onlay Collagen Dura Substitute Membrane due to unsealed outer packaging that may compromise product sterility and increase infection risk.

    Product
    DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches (10.0cm x 12.5cm) REF: CDSLM45
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0677-2022·2022-03-02

    Shoulder Implant Stem Recalled for Defective Coating Adhesion

    Biomet is recalling Comprehensive Shoulder System Mini Humeral Stems due to defective porous plasma coating adhesion. Internal testing indicated affected parts may lack sufficient coating strength.

    Product
    Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 15 MM, 83 MM Long Item Number: 113635
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0673-2022·2022-03-02

    Biomet Shoulder Stem Implants Recalled for Coating Adhesion Defect

    Biomet is recalling certain shoulder stem implants due to potential insufficient adhesion strength in the porous plasma coating. An improper rework process may have compromised the coating's integrity.

    Product
    Comprehensive Shoulder System Primary Shoulder Stem, Micro Length, Porous Plasma, 18 MM, 55 MM Long Item Number: 113618
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0674-2022·2022-03-02

    Comprehensive Shoulder System Mini Humeral Stem Recalled for Coating Adhesion Defect

    Biomet recalls 11 units of its Comprehensive Shoulder System Mini Humeral Stem due to potential coating adhesion defects. An unvalidated rework process was applied to vendor-coated parts, risking implant failure.

    Product
    Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 11 MM, 83 MM Long Item Number: 113631
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0740-2022·2022-03-02

    EpiGenius Kids Chocolate Superfood Recalled for Undeclared Milk

    Organic By Nature, Inc. is recalling Purim Health Brands EpiGenius Kids Chocolate: Daily Superfood pouches due to undeclared milk in an MCT powder ingredient. The product poses a risk to consumers with milk allergies.

    Product
    Purim Health Brands EpiGenius Kids Chocolate: Daily Superfood 630 g pouches Suggested Use: Mix approximately three tablespoons with 8-10 ounces of cold water. Shake vigorously or blend. For a creamier texture, mix with your favorite non-diary milk or in smoothie. This delicious
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0664-2022·2022-03-02

    Stryker Color Cuff tourniquet cuff mislabeled as single-bladder when dual-bladder

    Stryker Sustainability Solutions is recalling 40 units of Color Cuff 18" tourniquet cuffs (Lot #12983349) because they are mislabeled as single-bladder when they are actually dual-bladder, creating a risk of incorrect clinical use.

    Product
    REF: 5921-018-135, Stryker Color Cuff, 18" (Red), Quick Connect Single Port, Single Bladder
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0675-2022·2022-03-02

    Biomet Shoulder Implant Stem Coating Adhesion Defect Recall

    Biomet is recalling shoulder implant stems due to improper rework of porous plasma coating, which may lack sufficient adhesion strength. Affected units may fail if the coating detaches.

    Product
    Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 12 MM, 83 MM Long Item Number: 113632
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0591-2022·2022-03-02

    UP AND UP Children's Acetaminophen Oral Suspension Recalled for Contaminated Excipient

    Perrigo Company PLC is recalling UP AND UP Children's Acetaminophen Oral Suspension (160mg/5ml, 4 FL OZ bottles) because the product was manufactured with a contaminated excipient that was recalled by the supplier. The recall affects approximately 26,832 bottles distributed nationwide.

    Product
    UP AND UP CHILDRENS ACETAMINOPHEN — UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0597-2022·2022-03-02

    Parents Choice Infant Acetaminophen Recalled for Contaminated Excipient

    Perrigo Company is recalling approximately 55,656 bottles of Parents Choice Infants Pain and Fever (Acetaminophen) oral suspension nationwide due to CGMP deviations. The product was manufactured with a contaminated excipient that was recalled from the supplier.

    Product
    PARENTS CHOICE INFANTS PAIN AND FEVER — PARENTS CHOICE INFANTS PAIN AND FEVER (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0619-2022·2022-03-02

    Perrigo Nasal Oxymetazoline Spray Recalled for Contaminated Excipient

    Perrigo Company PLC is recalling approximately 10,800 bottles of NASAL Maximum Strength No Drip Nasal Spray (Oxymetazoline HCl 0.05%) nationwide due to manufacturing with a contaminated excipient supplied by their ingredient vendor.

    Product
    NASAL — NASAL (OXYMETAZOLINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0601-2022·2022-03-02

    UP AND UP Childrens Acetaminophen Recall Due to Contaminated Excipient

    Perrigo Company is recalling UP AND UP Childrens Acetaminophen oral suspension due to contamination from a recalled excipient used in manufacturing. The product was distributed nationwide.

    Product
    UP AND UP CHILDRENS ACETAMINOPHEN — UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0656-2022·2022-03-02

    Medline Michels Transport Medium Recalled for Improper Storage Conditions

    Medline is recalling 2,816 Michels Transport Medium prefilled containers due to improper storage in a temperature-controlled setting instead of refrigeration.

    Product
    Michels Transport Medium, 20ML Prefilled Cont
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0618-2022·2022-03-02

    Soothing 12 Hour Nasal Decongestant Spray Recall Due to Contaminated Excipient

    Perrigo Company PLC is recalling Soothing 12 Hour Nasal Decongestant Spray nationwide because the product was manufactured with a contaminated excipient that was recalled from the supplier.

    Product
    Soothing 12 Hour Nasal Decongestant Spray No Drip, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, Distributed By MAJOR PHARMACEUTICALS, 17177 N Laurel Park Drive, Suite 233 Livonia, MI 48152. NDC 0904-6761-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0577-2022·2022-03-02

    Bortezomib 3.5 mg Vials Recalled Due to Failed Stability Specifications

    Dr. Reddy's Laboratories is recalling Bortezomib 3.5 mg single-dose vials nationwide due to failed stability specifications. Approximately 2,980 vials of lot H210233 (expiration 3/1/2023) are affected.

    Product
    Bortezomib, 3.5 mg/vial, Single-Dose Vial, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046, India, NDC 43598-865-60
    Category
    Drug
    Distribution
    Distributed nationwide

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