The Recall Desk

Archive

March 2017 recalls

854 recalls were announced in March 2017.

What the numbers show

Critical
90
Severe
216
High
382
Moderate
134
Low
32

Of the 854 recalls this month scored against our rubric, 11% are Critical, 25% are Severe.

701–800 of 854

  • ModerateFDA (Drugs)·D-0507-2017·2017-03-08

    Dr. Reddy's Recalls Zenatane Capsules Due to Dissolution Failures

    Dr. Reddy's Laboratories is recalling specific lots of Zenatane (isotretinoin) 20 mg capsules because they failed to meet dissolution specifications.

    Product
    ZENATANE — ZENATANE (ISOTRETINOIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0490-2017·2017-03-08

    Cyclosporine Capsules Recalled for Impurity Specification Failures

    Amerisource Health Services is recalling 454 cartons of Cyclosporine Capsules, 100 mg, due to failed impurity specifications.

    Product
    CYCLOSPORINE — CYCLOSPORINE (CYCLOSPORINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1254-2017·2017-03-08

    Siemens ADVIA Centaur Calibrator A Kits Recalled for FT4 Bias

    Siemens recalls ADVIA Centaur Calibrator A kits due to negative bias in FT4 assays and potential calibration failures on specific systems.

    Product
    Siemens ADVIA Centaur Systems Calibrator A Kits, Cat No. 04800646, SMN 10285903 (2 pack)Cat No. 04800735, SMN 10285904 (6 pack) Cat No. 04800840, SMN 10285905 (6 pack - REF)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1394-2017·2017-03-08

    BD AffirM VPIII Microbial Identification Test Recalled for Invalid Results

    Becton Dickinson is recalling specific lots of the BD AffirM VPIII Microbial Identification Test because blue speckles or fibers may cause invalid test results.

    Product
    BD AffirM VPIII Microbial Identification Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1396-2017·2017-03-08

    McKesson Radiology PACS Software Recall for Potential Missing Images

    McKesson Medical Imaging is recalling McKesson Radiology 12.2 PACS software due to a defect that may cause missing images or stuck imports.

    Product
    McKesson Radiology 12.2 - Picture Archive Communication System (PACS)
    Category
    Medical Device
    Distribution
    14 states
  • ModerateFDA (Drugs)·D-0506-2017·2017-03-08

    Dr. Reddy's Recalls Zenatane Capsules for Dissolution Failure

    Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) capsules because they failed to meet dissolution specifications. The affected lot is distributed nationwide.

    Product
    ZENATANE — ZENATANE (ISOTRETINOIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1256-2017·2017-03-08

    Siemens ADVIA Centaur Calibrator A Kits Recalled for FT4 Bias

    Siemens is recalling specific Calibrator A kits due to confirmed negative bias and potential calibration failures for the FT4 assay on certain ADVIA Centaur systems.

    Product
    Siemens ADVIA Centaur Systems Calibrator A Kits, Cat No. 04800646, SMN 10285903 (2 pack)Cat No. 04800735, SMN 10285904 (6 pack) Cat No. 04800840, SMN 10285905 (6 pack - REF)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1382-2017·2017-03-08

    Matrix Surgical Recalls Mislabelled Mandible Onlay Implants

    Matrix Surgical Holdings is recalling 28 mandible onlay implants due to packaging mislabeling where left-sided packaging contained right-sided devices.

    Product
    OP7543 Design Y Mandible Onlay - Medium - Left and OP7544 Design Y Mandible Onlay - Medium - Right
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1395-2017·2017-03-08

    MED-EL SONNET Mini Battery Pack Cable Recall for Welding Defect

    MED-EL is recalling 538 SONNET Mini Battery Pack Cables because the compartment lock was not firmly welded to the housing.

    Product
    SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery Pack Cable is part of the SONNET Mini Battery Pack, which is an external battery pack used to power one MED-EL SONNET control unit. It can be worn on the upper body or the hip using different SONNET Mini Batter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0508-2017·2017-03-08

    Dr. Reddy's Recalls Zenatane Capsules for Dissolution Failure

    Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) 30 mg capsules because they failed to meet dissolution specifications.

    Product
    Zenatane (isotretinoin) capsules, 30 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By:Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 5511-113-81
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0502-2017·2017-03-08

    Sun Pharmaceutical Recalls Alfuzosin Hydrochloride Tablets Due to Foreign Matter

    Sun Pharmaceutical Industries is recalling specific lots of Alfuzosin Hydrochloride Extended-release Tablets because a consumer complaint identified a broken piece of wire rope embedded in a tablet.

    Product
    ALFUZOSIN HYDROCHLORIDE — ALFUZOSIN HYDROCHLORIDE (ALFUZOSIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0500-2017·2017-03-08

    Allegiant Health Recalls HealthA2Z Chewable Aspirin Due to Rubber Particles

    Allegiant Health is recalling HealthA2Z Chewable Aspirin 81 mg because rubber particles were found in the bulk product.

    Product
    HealthA2Z CHEWABLE Aspirin (NSAID) 81 mg, Orange Flavor, 36 Chewable Tablets, a) packaged in 36-count bottle [UPC Code 369168288362 (FP0545)], b) bulk product (6K28817), OTC, Manufactured by: Allegiant Health Deer Park, NY 11729
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0509-2017·2017-03-08

    Dr. Reddy's Recalls Zenatane Capsules Due to Dissolution Failure

    Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) capsules because they failed to meet dissolution specifications. The recall covers 4,404 cartons distributed nationwide.

    Product
    ZENATANE — ZENATANE (ISOTRETINOIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0503-2017·2017-03-08

    Perrigo Recalls Salicylic Acid Shampoo Due to Organic Impurity

    L. Perrigo Company is recalling Salicylic Acid Shampoo, 6%, because the active ingredient failed impurity specifications.

    Product
    Salicylic Acid Shampoo, 6%, 177 mL bottle, Rx only, Manufactured By Perrigo Yeruham, Israel, Distributed By Perrigo Allegan, MI 49010, NDC 45802-237-01, UPC 3 45802-237-01 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0504-2017·2017-03-08

    Perrigo Recalls Salicylic Acid Cream Due to Organic Impurity

    L. Perrigo Company is recalling Salicylic Acid Cream, 6%, due to an out-of-specification organic impurity. The FDA classified this as a Class III recall.

    Product
    Salicylic Acid Cream, 6%, 400g bottle, Rx Only, Manufactured By Perrigo Yeruham, Israel 80500, Distributed By Perrigo Allegan, MI 49010, NDC 45802-806-01, UPC 3 45802-806-01 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0788-2017·2017-03-08

    Medtronic SynchroMed II Software Card Recall for Priming Bolus Function

    Medtronic is recalling 22,298 SynchroMed II software application cards to update the priming bolus function and pump labeling.

    Product
    Medtronic SynchroMed II Implantable Drug Infusion System. This system includes: Model 8870 Software Application Card, Model 8840 N'Vision Clinician Programmer, and Model 8637 SynchroMed II Implantable Drug Infusion Pump (supplied in 20 ml or 40 ml reservoir size.) Product
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V149000·2017-03-07

    Mercedes-Benz and Freightliner Sprinter Vehicles Recalled for Driveshaft Welding Defect

    Daimler Vans USA is recalling 2016 Mercedes-Benz and Freightliner Sprinter 2500 and 3500 vehicles because a driveshaft bracket may not be properly welded, posing a fire risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E014000·2017-03-07

    H&H Sports Protection Recalls TORC T-55 V2 Motorcycle Helmets

    H&H Sports Protection is recalling TORC T-55 V2 half helmets because they may not adequately protect the wearer or stay secured during a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V148000·2017-03-07

    Mercedes-Benz Metris Recall for Non-Functioning Blind Spot Monitoring

    Daimler Vans USA is recalling 2016-2017 Mercedes-Benz Metris vans because the Blind Spot Monitoring system does not work due to incompatible parts.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17733·2017-03-07

    L.L. Bean Recalls Snowshoes Due to Plastic Frame Breakage Hazard

    L.L. Bean is recalling Adventure Adjustable Snowshoes because the plastic deck can weaken and break, posing a fall hazard. No injuries have been reported.

    Product
    Snowshoes and snowshoe packages
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V144000·2017-03-06

    Nissan Recalls 2012 Versa Vehicles Due to Air Bag Deployment Risk

    Nissan is recalling 54,751 2012 Versa vehicles because degraded side impact sensor connector pins may cause air bags to deploy unexpectedly if a door is slammed.

    Product
    NISSAN — NISSAN VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V141000·2017-03-06

    Forest River Recalls 2017 Prime Time Crusader Trailers for Placard Error

    Forest River is recalling 2017 Prime Time Crusader recreational trailers because the Federal placard incorrectly lists axle capacity as 7,000 lbs instead of 6,000 lbs, which could lead to overloading.

    Product
    PRIME TIME — PRIME TIME CRUSADER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V143000·2017-03-06

    Nissan Recalls 2017 Infiniti QX30 for Driver-Side Air Bag Defect

    Nissan is recalling 2017 Infiniti QX30 vehicles because the driver-side curtain air bag may fail to deploy in a crash, increasing injury risk.

    Product
    INFINITI — INFINITI QX30
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·021-2017·2017-03-06

    F.B. Packing Co. Recalls Shaved Beef Products Due to Plastic Contamination

    F.B. Packing Co. is recalling approximately 8,430 pounds of shaved beef products that may contain plastic strands. The recall covers products shipped to retail locations in Illinois and Massachusetts.

    Product
    Bertolino Foods, Inc. — F.B. Packing Co., Inc. Recalls Beef Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    2 states
  • LowUSDA FSIS·022-2017·2017-03-06

    Rochester Meat Company Recalls Pork Sausage Products Due To Misbranding

    Rochester Meat Company is recalling approximately 13,330 pounds of pork sausage products because they contain undeclared monosodium glutamate (MSG). The products were shipped to institutional locations in five states.

    Product
    Branding Iron Holdings — Rochester Meat Company Recalls Pork Sausage Products Due To Misbranding
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·17V140000·2017-03-03

    REV Recalls Motorhomes Due to Improperly Secured Fuel Pump and Filter

    REV Recreation Group is recalling specific 2015-2017 Fleetwood and Holiday Rambler motorhomes because an improperly secured fuel pump or filter may leak fuel, increasing the risk of fire or explosion.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER STORM, ADMIRAL XE, FLAIR, TERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V139000·2017-03-03

    REV Recalls American Coach and Holiday Rambler Motorhomes for Step Defect

    REV Recreation Group is recalling specific 2015-2017 American Coach and Holiday Rambler motorhomes because interior step supports may be inadequately secured, creating an injury risk.

    Product
    AMERICAN COACH — AMERICAN COACH, HOLIDAY RAMBLER AMERICAN EAGLE, AMERICAN DREAM, AMERICAN TRADITION, AMERICAN HERITAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17102·2017-03-02

    Polaris Recalls RZR and GENERAL Off-Highway Vehicles for Fire Hazards

    Polaris is recalling about 13,500 RZR and GENERAL off-highway vehicles due to engine misfires and brake issues that can cause fires and burns.

    Product
    Polaris recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V138000·2017-03-02

    BMW Recalls X5 and X6 Models for Driveshaft Wear Risk

    BMW is recalling 2011-2014 X5 and X6 vehicles because water and debris may cause the front driveshaft universal joint to fail, potentially affecting traction and increasing crash risk.

    Product
    BMW — BMW X5, X6, X6 ACTIVEHYBRID SAC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V133000·2017-03-02

    Porsche Recalls Macan Models Due to Passenger Air Bag Sensor Defect

    Porsche is recalling 2015-2017 Macan models because a faulty sensor may deactivate the front passenger air bag, increasing injury risk in a crash.

    Product
    PORSCHE — PORSCHE MACAN S, MACAN TURBO, MACAN GTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17103·2017-03-02

    Goodman Recalls Air Handlers Due to Electrical Shock Hazard

    Goodman is recalling approximately 210,000 air handler units because the pull-out disconnects may fail to disable power, posing an electrical shock hazard to individuals servicing the equipment.

    Product
    Air handlers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V134000·2017-03-02

    Porsche Recalls 2016-2017 911 and 718 Models for Air Bag Defect

    Porsche is recalling 2016-2017 911 and 718 models because the passenger air bag inflator may fail to ignite, increasing injury risk in a crash.

    Product
    PORSCHE — PORSCHE 911, 911 CARRERA, 911 TARGA 4, 911 GT3 RS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V136000·2017-03-02

    Volkswagen Recalls 2017 Beetle and Jetta GLI for Incorrect Tire Labels

    Volkswagen is recalling 2017 Beetle and Jetta GLI vehicles because incorrect tire information labels may cause operators to overload the vehicle, increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA, BEETLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·020-2017·2017-03-02

    Ohio Farms Recalls Veal Products Due To Possible E. Coli O103 Contamination

    Ohio Farms Packing Co. Ltd. is recalling approximately 40,680 pounds of boneless veal products and an undetermined amount of veal cutlets due to possible E. coli O103 contamination.

    Product
    Ohio Farms Packing Co. Ltd. — Ohio Farms Packing Co. Ltd. Recalls Veal Products Due To Possible E. Coli O103 Contamination
    Category
    Food
    Distribution
    7 states
  • HighCPSC·17104·2017-03-02

    Kids II Recalls Oball Rattles Due to Choking Hazard

    Kids II is recalling Oball Rattles because the plastic disc can break, releasing small beads that pose a choking hazard to young children.

    Product
    Oball Rattles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V132000·2017-03-02

    Subaru Recalls 2017 Impreza for Rearview Camera Software Issue

    Subaru is recalling 2017 Impreza vehicles because a software problem may cause the rearview camera display to malfunction, increasing crash risk.

    Product
    SUBARU — SUBARU IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17101·2017-03-02

    Ryobi Electric Jet Fan Blowers Recalled for Laceration Hazard

    One World Technologies is recalling Ryobi 8amp Electric Jet Fan Blowers because the internal plastic fan can break, discharging blades that pose a laceration hazard.

    Product
    Ryobi Electric Jet Fan Blowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateNHTSA·17V137000·2017-03-02

    Volkswagen Recalls 2017 Jetta for Incorrect Tire Information Label

    Volkswagen is recalling 2017 Jetta vehicles because incorrect tire information labels may lead to vehicle overloading, increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1512-2017·2017-03-01

    Palmer's Candies Chocolatey Tree Pretzels Recalled for Salmonella Risk

    Palmer and Company is recalling 716 cases of Chocolatey Tree Pretzels because a supplier ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies Chocolatey Tree Pretzels NET WT 28 lbs (12.7 kg), packaged cardboard boxes, UPC 77232-10799
    Category
    Food
    Distribution
    34 states
  • CriticalFDA (Food)·F-1499-2017·2017-03-01

    Palmer's Candies Drizzled Peanuts Brittle Recalled for Salmonella Risk

    Palmer and Company is recalling Drizzled Peanuts Brittle because an ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies Drizzled Peanuts Brittle A) NET WT 8 OZ (226 g) packaged in plastic clamshell containers, UPC 77232-17002; B) 20 lbs. Net Weight (9.07 kg) packaged in cardboard boxes UPC 77232-10809
    Category
    Food
    Distribution
    34 states
  • CriticalFDA (Food)·F-1494-2017·2017-03-01

    Hy-Vee Cookie and Candy Recalled for Potential Salmonella Contamination

    Hy-Vee Stores Inc is recalling specific Cookie & Candy products due to a potential Salmonella contamination risk from a supplier ingredient.

    Product
    Cookie & Candy packaged in a 9"/16oz. (UPC 026138600000), 12" /32 oz. (UPC 026138700000), and 16"/48 oz. (UPC 026138800000) plastic tray containers for retail sale, labeled with Hy-Vee scale ticket. The product was labeled HyVee West Des Moines, IA.
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1503-2017·2017-03-01

    Palmer's Candies Christmas Tree Pretzels Recalled for Salmonella Risk

    Palmer's Candies is recalling Christmas Tree Pretzels because an ingredient may be contaminated with Salmonella. The product was distributed to grocery stores in 34 states.

    Product
    Palmer's Candies Bakery Delights Christmas Tree Pretzels NET WT 5 OZ (141 g) packaged in foil bags, UPC Code 77232-13227
    Category
    Food
    Distribution
    34 states
  • CriticalFDA (Food)·F-1504-2017·2017-03-01

    Palmer's Candies Swirled Pretzels Recalled Due to Salmonella Risk

    Palmer and Company is recalling Swirled Pretzels because an ingredient may be contaminated with Salmonella. The product was distributed to grocery stores in 34 states.

    Product
    Palmer's Candies Swirled Pretzels NET WT 5 OZ (141 g) packaged in foil bags, UPC Code 77232-13990
    Category
    Food
    Distribution
    34 states
  • CriticalFDA (Food)·F-1496-2017·2017-03-01

    Palmer's Candies Christmas Tree Pretzels Recalled for Salmonella Risk

    Palmer and Company is recalling Christmas Tree Pretzels because an ingredient may be contaminated with Salmonella. The product was distributed to grocery stores in 34 states.

    Product
    Palmer's Candies Christmas Tree Pretzel, NET WT 7 OZ (198 g) packaged in plastic clamshell container, UPC Code A) 77232-16310 and B) 77232-17137
    Category
    Food
    Distribution
    34 states
  • CriticalFDA (Food)·F-1534-2017·2017-03-01

    Fromi USA Recalls Tomme Brebis Fedou Cheese Due to Listeria Risk

    Fromi USA Corp is recalling Tomme Brebis Fedou cheese in California, New York, and Massachusetts due to potential Listeria monocytogenes contamination.

    Product
    Tomme Brebis Fedou, Net Wt. 9.7lb (case)/Net Wt 4.85 lb per unit, Item number 702084
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-1501-2017·2017-03-01

    Palmer's Candies Recalled for Potential Salmonella Contamination

    Palmer and Company is recalling specific holiday candy products because an ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies A) Holiday Treats NET WT 15.5 OZ (439 g) packaged in plastic containers, UPC Code 77232-23045; B) Holiday Gift Bowl NET WT 22 OZ (623 g) packaged in plastic containers, UPC 77232-17285; C) Variety Christmas Bowl NET WT 15 OZ (425 g), packaged in plastic container
    Category
    Food
    Distribution
    34 states
  • CriticalFDA (Food)·F-1507-2017·2017-03-01

    Palmer's Candies Chocolate Pastel Pretzels Recalled for Salmonella Risk

    Palmer and Company is recalling Palmer's Candies Chocolate Pastel Pretzels because an ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies Chocolate Pastel NP Pretzels NET WT 28 lbs (12.7 kg), packaged cardboard boxes, UPC 77232-10783
    Category
    Food
    Distribution
    34 states
  • CriticalFDA (Food)·F-1489-2017·2017-03-01

    Hy-Vee Crème De Menthe Almond Bark Recalled for Salmonella Risk

    Hy-Vee is recalling Crème De Menthe Almond Bark because a supplier ingredient may be contaminated with Salmonella.

    Product
    Cr¿me De Menthe Almond Bark packaged 12 oz. (UPC 026266300000) plastic tray containers for retail sale, labeled with Hy-Vee scale ticket. The product was labeled HyVee West Des Moines, IA.
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1535-2017·2017-03-01

    True World Foods Recalls Ogo Seaweed Due to Salmonella Link

    True World Foods Portland, LLC is recalling Ogo (seaweed) because the raw material was harvested from a farm linked to Salmonella illnesses in Hawaii.

    Product
    Ogo (Seaweed) packaged in plastic bags. Label contains the product name, date of shipment, weight of the order, toute number, order number and Distributed By True World Foods Portland LLC.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1533-2017·2017-03-01

    Fromi USA Recalls Soureliette Cheese Due to Listeria Contamination

    Fromi USA Corp is recalling specific lots of Soureliette cheese due to Listeria monocytogenes contamination. The product was distributed in California, New York, and Massachusetts.

    Product
    Soureliette cheese, Net Wt 3.969 lb (case)/ Net Wt 1.323 lb per unit, Item number 707116
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-1508-2017·2017-03-01

    Palmer's Chocolate Pretzels Recalled for Potential Salmonella Contamination

    Palmer and Company is recalling Palmer's Candies Chocolate Pretzels with Frosted Swirl because a supplier ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies Chocolate Pretzels with Frosted Swirl NET WT 28 lbs (12.7 kg), packaged cardboard boxes, UPC 77232-10743
    Category
    Food
    Distribution
    34 states
  • CriticalFDA (Food)·F-1506-2017·2017-03-01

    Palmer Candy Recalls Peppermint Pretzels Due to Salmonella Risk

    Palmer Candy Co is recalling specific lots of Peppermint Pretzels because an ingredient may be contaminated with Salmonella.

    Product
    A) Peppermint Pretzels NET WT 5 OZ (141 g), packaged in foil bags, UPC 25439-20204; B) Mix Peppermint Pretzels NET WT 7 OZ, UPC 77232-12147
    Category
    Food
    Distribution
    34 states
  • CriticalFDA (Food)·F-1511-2017·2017-03-01

    Palmer's Candies Heart Pretzels Recalled for Potential Salmonella Contamination

    Palmer and Company is recalling 54 cases of Palmer's Candies Chocolatey Flavored NP Heart Pretzels because an ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies Chocolatey Flavored NP Heart Pretzels NET WT 28 lbs (12.7 kg), packaged cardboard boxes, UPC 77232-10778
    Category
    Food
    Distribution
    34 states
  • CriticalFDA (Food)·F-1490-2017·2017-03-01

    Hy-Vee Dazzled Peanut Brittle Recalled for Potential Salmonella Contamination

    Hy-Vee is recalling Dazzled Peanut Brittle because it contains an ingredient that may be contaminated with Salmonella. The product was sold in Hy-Vee stores in eight states.

    Product
    Dazzled Peanut Brittle packaged in 8oz. (UPC 026267300000) and 12 oz. (UPC 026267400000) plastic tray containers for retail sale, labeled with Hy-Vee scale ticket. The product was labeled HyVee West Des Moines, IA.
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1493-2017·2017-03-01

    Hy-Vee Candy Recalled Due to Potential Salmonella Contamination

    Hy-Vee Stores Inc is recalling candy sold in plastic trays because an ingredient may be contaminated with Salmonella.

    Product
    Candy packaged in a 9"/16oz. (UPC 026138000000), 12" /32 oz. (UPC 026138100000), and 16"/48 oz. (UPC 026138200000) plastic tray containers for retail sale, labeled with Hy-Vee scale ticket. The product was labeled HyVee West Des Moines, IA.
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0482-2017·2017-03-01

    RemedyRepack Recalls Glipizide Tablets for Failed Dissolution Specifications

    RemedyRepack Inc. is recalling Glipizide 2.5 mg ER tablets because they failed to meet dissolution specifications. The product was distributed to a customer in Florida.

    Product
    Glipizide 2.5 mg ER Tablets, Manufactured by Watson Laboratories, Inc., Parsippany, NJ 07054, Repackaged by RemedyRepack, Indiana, PA 15701, NDC 52125-0764-02
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0475-2017·2017-03-01

    Apotex Recalls Cyclosporine Capsules Due to Impurity Failures

    Apotex Inc. is recalling 19,584 bottles of Cyclosporine Capsules, USP, 100 mg, because the product failed impurity specifications.

    Product
    CYCLOSPORINE — CYCLOSPORINE (CYCLOSPORINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1488-2017·2017-03-01

    Hy-Vee Chocolate Almond Pretzels Recalled for Salmonella Risk

    Hy-Vee is recalling chocolate almond pretzels because an ingredient may be contaminated with Salmonella. The product was sold in eight states.

    Product
    Chocolate almond pretzels packaged in 4 oz. (UPC 026131900000) and 12 oz. (UPC 026131800000) plastic tray containers for retail sale, labeled with Hy-Vee scale ticket. The product was labeled HyVee West Des Moines, IA.
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0480-2017·2017-03-01

    Hospira Recalls Metronidazole Injection Bags Due to Leaking

    Hospira is recalling 578,784 bags of Metronidazole Injection due to a customer report of a leaking bag, which compromises sterility assurance.

    Product
    METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira Inc., Lake Forest, IL --- NDC 0409-7811-24
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1497-2017·2017-03-01

    Palmer's Candies Cookies & Cream Bark Recalled for Salmonella Risk

    Palmer and Company is recalling Palmer's Candies Cookies & Cream Bark because an ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies Cookies & Cream Bark, NET WT 9 OZ (255 g) packaged in plastic clamshell container, UPC Code 77232-17254
    Category
    Food
    Distribution
    34 states
  • SevereNHTSA·17V131000·2017-03-01

    REV Recalls 2017 Ambulances Due to Rear Brake Bolt Torque Issue

    REV Ambulance Group is recalling 69 specific 2017 Type I ambulances because overtightened rear brake bolts may cause loss of braking power.

    Product
    MARQUE — MARQUE, FRONTLINE, WHEELED COACH TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·019-2017·2017-03-01

    Dos Hermanos Recalls Beef Jerky Produced Without Federal Inspection

    Dos Hermanos, Inc. is recalling approximately 151 pounds of Carne Seca Beef Jerky produced without federal inspection. The products were distributed in Illinois, Iowa, Kansas, and Missouri.

    Product
    Dos Hermanos, Inc. Recalls Beef Jerky Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1164-2017·2017-03-01

    Biomet Recalls Oxford Partial Knee Instruments Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • SevereFDA (Devices)·Z-1165-2017·2017-03-01

    Biomet Recalls Oxford Partial Knee Trial Trays Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System trial trays due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Oxford Partial Knee System Left Medial Tibial Trial Tray Size C
    Category
    Medical Device
    Distribution
    14 states
  • SevereFDA (Food)·F-1510-2017·2017-03-01

    Palmer's Chocolatey Pretzels Recalled for Potential Salmonella Contamination

    Palmer and Company is recalling 198 cases of Palmer's Candies Chocolatey Pretzels because an ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies Chocolatey Pretzels NET WT 28 lbs (12.7 kg), packaged cardboard boxes, UPC 77232-10798
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Devices)·Z-1167-2017·2017-03-01

    Biomet Recalls Oxford Knee Instruments Due to Material Inclusions

    Biomet U.K. is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Left Medial Tibial Trial Tray Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • SevereFDA (Food)·F-1492-2017·2017-03-01

    Hy-Vee Holiday Candy Recalled Due to Potential Salmonella Contamination

    Hy-Vee Stores Inc. is recalling Holiday Candy in various plastic tray sizes because an ingredient may be contaminated with Salmonella.

    Product
    Holiday Candy packaged in a 10"/16oz. (UPC 026139100000), 12" /32 oz. (UPC 026139300000), 16"/48 oz. (UPC 026139500000), and 18"/64 oz. (UPC 026139700000) plastic tray containers for retail sale, labeled with Hy-Vee scale ticket. The product was labeled HyVee West Des Moines, IA
    Category
    Food
    Distribution
    8 states
  • SevereNHTSA·17V130000·2017-03-01

    New Flyer Transit Buses Recalled for Front Axle Beam Cracks

    New Flyer is recalling 2,357 transit buses from 2005-2007 because front axle beams may crack and fail, risking loss of vehicle control.

    Product
    NEW FLYER — NEW FLYER GE40LF, D60LFR, D60LF, C35LF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·018-2017·2017-03-01

    Procesadora La Hacienda Recalls Raw Meat Products Due to Undeclared Allergens

    Procesadora La Hacienda is recalling raw seasoned meat products because they contain undeclared wheat and milk allergens. No adverse reactions have been reported.

    Product
    Procesadora La Hacienda, Inc. — Procesadora La Hacienda, Inc. Recalls Meat Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1495-2017·2017-03-01

    Palmer's Candies Chocolate Almond Bark Recalled for Salmonella Risk

    Palmer and Company is recalling specific chocolate almond bark products because an ingredient may be contaminated with Salmonella.

    Product
    A) Palmer's Candies Chocolate Almond Bark , NET WT 9 OZ (255 g) packaged in plastic clamshell container, UPC 77232-17250; B) Publix Bakery Almond Bark with Cocoa, NET WT 10 OZ (283 g), packaged in paper bags, UPC 77232-22691; C) Palmer's Candies Chocolate Almond Bark, 10 lbs. Net
    Category
    Food
    Distribution
    34 states
  • HighFDA (Food)·F-1514-2017·2017-03-01

    Hostess Recalls Holiday White Peppermint Twinkies Due to Salmonella Risk

    Hostess Brands is recalling Holiday White Peppermint Twinkies because an ingredient may be contaminated with Salmonella. The product was distributed nationwide.

    Product
    Holiday White Peppermint Hostess Twinkies, cream-filled snack cakes, Net Wt. 13.02 oz. (369 g), UPC 888109111571.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1157-2017·2017-03-01

    Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Left Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Food)·F-1487-2017·2017-03-01

    Hy-Vee Chocolate Almond Bark Recalled for Potential Salmonella Contamination

    Hy-Vee Stores Inc. is recalling chocolate almond bark because it contains an ingredient that may be contaminated with Salmonella.

    Product
    Chocolate almond bark packaged in 4 oz. (UPC 026133400000) and 12 oz. (UPC 021633300000) plastic tray containers for retail sale, labeled with Hy-Vee scale ticket. The product was labeled HyVee West Des Moines, IA.
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-1491-2017·2017-03-01

    Hy-Vee Peppermint Bark Recalled Due to Potential Salmonella Contamination

    Hy-Vee Stores Inc is recalling Peppermint Bark products because an ingredient may be contaminated with Salmonella. The recall affects specific retail stores in eight states.

    Product
    Peppermint Bark packaged in 4oz. (UPC 026133800000),12 oz. (UPC 026133700000) plastic tray containers, and 9 oz. tubs (UPC 026267900000) for retail sale, labeled with Hy-Vee scale ticket. The product was labeled HyVee West Des Moines, IA.
    Category
    Food
    Distribution
    8 states
  • HighNHTSA·17V129000·2017-03-01

    Forest River Recalls 2017 Rockwood and Flagstaff Trailers for Tire Defect

    Forest River is recalling 2017 Rockwood and Flagstaff recreational trailers because a slide room bracket may damage the front tire, causing deflation and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD, FLAGSTAFF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1526-2017·2017-03-01

    Golden Flake Potato Chips Recalled for Undeclared Milk

    Golden Flake is recalling Hot Thin & Crispy Potato Chips due to undeclared milk, a major allergen. The recall covers 14 states.

    Product
    Golden Flake (R) HOT THIN & CRISPY POTATO CHIPS, NET WT. 5 OZ. (141.8g), Golden Flake Snack Foods, Inc., Birmingham, AL 35201, UPC 0-72080-00240-3
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-1525-2017·2017-03-01

    Trader Joe's Harvest Whole Wheat Bread Recalled for Undeclared Milk Allergen

    Athens Baking Company is recalling specific lots of Trader Joe's Harvest Whole Wheat Bread because they fail to declare cultured whey or list milk as an allergen.

    Product
    Trader Joe's Harvest Whole Wheat Bread; NET WT 24 oz. (1 lb. 8 oz.) SKU 00132; UPC: 0000 1328. Distributed and sold exclusively by: Trader Joe's, Monrovia, CA 91016
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1523-2017·2017-03-01

    Archer Daniels Midland Recalls Dry Roasted Almonds for Undeclared Cashews

    Archer Daniels Midland is recalling one lot of dry roasted almonds because they may contain undeclared cashews. The product was distributed in California.

    Product
    Specialty Commodities, Inc., Almond, Dry RNS, SKU 0020034064 Item number ALMO-033, 25 lb carton.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1502-2017·2017-03-01

    Palmer's Candies Peppermint Bark Recalled for Potential Salmonella Contamination

    Palmer and Company is recalling Peppermint Bark candy because an ingredient may be contaminated with Salmonella. The product was distributed to grocery stores in 34 states.

    Product
    Palmer's Candies Peppermint Bark A) NET WT 9 OZ (255 g) packaged in plastic clamshell containers, UPC Code 77232-17270; B) NET WT 10 OZ (283 g) packaged in paper bags, UPC 77232-23091; C) NET WT 8 OZ (226 g) packaged in paper boxes UPC 77232-12146; C) NET WT 9 OZ (255 g) packaged
    Category
    Food
    Distribution
    34 states
  • HighFDA (Food)·F-1498-2017·2017-03-01

    Palmer's Candies Creme De Menthe Bark Recalled for Salmonella Risk

    Palmer and Company is recalling Palmer's Candies Creme De Menthe Bark because an ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies Creme De Menthe Bark, A) NET WT 9 OZ (255 g) packaged in cardboard boxes, UPC Code 77232-16043, B) NET WT 9 OZ (255 g) packaged in plastic clamshell containers, UPS code 77232-17255; C) NET WT 10 lbs Net Weight (4.54 kg) packaged in cardboard boxes
    Category
    Food
    Distribution
    34 states
  • HighNHTSA·17V127000·2017-03-01

    Volvo Recalls 2017 Models for Side Air Bag Inflator Defect

    Volvo is recalling 2017 S60, V60, and XC60 vehicles because side air bag inflators may fail to ignite, preventing deployment in a crash.

    Product
    VOLVO — VOLVO V60, XC60, S60, V60CC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1505-2017·2017-03-01

    Palmer Candy Recalls Trail's End Chocolatey Crunch Due to Salmonella Risk

    Palmer Candy Co is recalling Trail's End Gourmet Chocolatey Crunch because an ingredient may be contaminated with Salmonella.

    Product
    Trail's End Gourmet Chocolatey Crunch A) NET WT 18 OZ (1.13 LB) 510 g, packaged in foil bags; B) NET WT 15 OZ packaged in foil bags;
    Category
    Food
    Distribution
    34 states
  • HighFDA (Food)·F-1529-2017·2017-03-01

    Mahatma Saffron Yellow Rice Mixes Recalled for Foreign Metal Material

    Riviana International is recalling Mahatma Saffron Yellow seasonings and long grain rice mixes due to the presence of foreign metal material.

    Product
    (a) Mahatma(R) Saffron YELLOW seasonings & LONG GRAIN RICE; Net Wt. 5 oz. (UPC 17400-10505) (b) Mahatma(R) Saffron YELLOW seasonings & LONG GRAIN RICE; Net Wt. 10 oz. (UPC 17400-10507) (c) Mahatma(R) Saffron YELLOW seasonings & LONG GRAIN RICE; Net Wt. 16 oz. (UPC 17400-10502)
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1527-2017·2017-03-01

    Falafel King Recalls Tzatziki Sauce for Undeclared Milk Allergen

    Falafel King is recalling 1,380 containers of Tzatziki Sauce due to undeclared milk on the label. The product was distributed in Colorado, New Mexico, Utah, and Nebraska.

    Product
    Falafel King Tzatziki Sauce. 10 ounce. Plastic container
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1155-2017·2017-03-01

    Biomet Recalls Oxford Partial Knee Instruments Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1153-2017·2017-03-01

    Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System Femoral Slap Hammers due to potential alumina inclusions that could cause the instruments to crack or separate.

    Product
    Oxford Partial Knee System Femoral Slap Hammer Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1234-2017·2017-03-01

    Custom Medical Specialties Recalls Biopsy Trays with Syringes Due to Sterility Concerns

    Custom Medical Specialties is recalling 80 biopsy trays containing syringes because the sterility of the syringes could not be assured. The affected products were distributed to Idaho and Oregon.

    Product
    CMS-2193-R7 and CMS-1911-R3 Custom Biopsy Tray containing a BD 10cc LL Syringe, Sterile, Manufactured for CMS Custom Medical Specialties, Inc.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1161-2017·2017-03-01

    Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Left Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states

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