The Recall Desk

Archive

February 2016 recalls

511 recalls were announced in February 2016.

What the numbers show

Critical
28
Severe
159
High
175
Moderate
135
Low
14

Of the 511 recalls this month scored against our rubric, 5% are Critical, 31% are Severe.

201–300 of 511

  • HighFDA (Food)·F-0376-2016·2016-02-17

    Kraft Singles Deli Deluxe American Slices Recalled for Choking Hazard

    Kraft Heinz is recalling specific lots of Kraft Singles Deli Deluxe American Slices because packaging film may remain on the cheese, posing a choking risk.

    Product
    Kraft Singles Deli Deluxe American Slices packaged in a blue box with white lettering.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0764-2016·2016-02-17

    Philips Allura Xper FD20 Ceiling Version Recalled for C-Arc Movement

    Philips is recalling 15 Allura Xper FD20 Ceiling version units because improper adjustment may cause the C-arc to continue moving after stopping.

    Product
    Philips Allura Xper FD20 Ceiling version only; 722028; imaging applications.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0789-2016·2016-02-17

    Richard Wolf Reusable Rotary Blade Recall Due to Weak Welds

    Richard Wolf Medical Instruments Corp. is recalling ten reusable rotary blade/abrader units due to weak welds that may cause the product to break during surgical use.

    Product
    Reuseable rotary blade/abrader, product number 899751305. The round burr is an attachment or accessory to the air-powered device intended for use during surgical procedures to cut hard tissue or bone and soft tissue. General hospital and plastic surgery use.
    Category
    Medical Device
    Distribution
    1 state
  • HighCPSC·16103·2016-02-17

    Michaels Recalls Artificial Poinsettias Due to Mold Exposure Risk

    Michaels is recalling Ashland artificial poinsettia stems and bushes because mold may be present, posing a risk of respiratory or other infections.

    Product
    Ashland Poinsettia Stems and Bushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0792-2016·2016-02-17

    Mizuho OSI Trios Table Base Recall for Missing Retaining Ring

    Mizuho OSI is recalling 33 Trios table bases because a missing retaining ring may cause the clutch to jam, preventing patient rotation.

    Product
    Mizuho OSI Trios, Table Base; Voltage: 100-240V ~ 50/60 Hz Amps: 5,0-5.0A; Model 7803 and 7803AP Orthopaedic: Operating room tablebase - an electronically powered mobile operating table is created, designed for temporary (<24 hours) support and positioning of a patient in
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0550-2016·2016-02-17

    Zingerman's Recalls Chocolate Marshmallows Due to Undeclared Soy

    Zingerman's Candy Manufactory is recalling 8-ounce bags of Chocolate Marshmallows because they contain undeclared soy. The recall affects 134 units distributed across 18 states and Washington, D.C.

    Product
    Chocolate Marshmallows, 8 oz., packaged in plastic bags, UPC 8 44397 00077 5
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-0761-2016·2016-02-17

    Del Medical VS200 Radiographic Cassette Holder Recall for Falling Hazard

    Del Medical is recalling VS200 radiographic cassette holders and wall stands because they can suddenly fall to the ground and contact patients.

    Product
    VS200 radiographic Cassette Holder or Wall Stand. For use in radiology department.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0771-2016·2016-02-17

    Accuray CyberKnife Robotic Recall for Potential Gun Box Mounting Bracket Failure

    Accuray is recalling CyberKnife Robotic systems because the gun box mounting bracket may fail, allowing the gun box to fall and contact a patient.

    Product
    CyberKnife Robotic; Catalog/part number 032000 and 033000 Cosmetic cover package. Product Usage: The CyberKnife Robotic Radiosurgery System is indicated for treatment planning and image guided stereotactic Radiosurgery and precision radiotherapy for lesions, tumors, and condi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0561-2016·2016-02-17

    Albertsons Recalls Coast to Coast Sourdough Hoagie Rolls Due to Foreign Material

    Albertsons Companies, Inc. is recalling Coast to Coast San Francisco Style Sourdough 6 Hoagie Rolls because cloth material from production equipment may be present in the product.

    Product
    Coast to Coast San Francisco Style Sourdough 6 Hoagie Rolls; 6 Hoagie Rolls; NET WT 16.5 oz 468 g UPC 0 21130 18091 2; Distributed by Living Better Brands, LLC, Pleasanton, CA 94566 Contains: Wheat May Contain eggs, milk.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0301-2016·2016-02-17

    E3 Artisan Recalls Dark Chocolate Bars Due to Undeclared Milk

    E3 Artisan is recalling 636 dark chocolate bars because FDA testing found undeclared milk, a major food allergen, in the product.

    Product
    Inclusion chocolate bar 66% Cacao topped with pistachios, cranberries & Sea Salt in a white and green wrapping with white and gray lettering.
    Category
    Food
    Distribution
    0 states
  • HighNHTSA·16V089000·2016-02-17

    Keystone Recalls 2016 Sprinter RVs Due to Falling Television Risk

    Keystone is recalling 2016 Sprinter recreational vehicles because a wall-mounted television may break off, posing an injury risk to occupants.

    Product
    KEYSTONE — KEYSTONE SPRINTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V090000·2016-02-17

    Navistar Recalls 2016 IC CE Buses for Hood Strap Defect

    Navistar is recalling 104 model year 2016 IC CE commercial buses because hood straps may elongate, causing the hood to open unexpectedly during braking and obstructing the driver's vision.

    Product
    IC BUS — IC BUS CE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0375-2016·2016-02-17

    Kraft Singles White American Recalled for Potential Choking Hazard

    Kraft Heinz is recalling Kraft Singles White American cheese slices because packaging film may remain on the slice, posing a choking risk.

    Product
    Kraft Singles White American singles packaged in a blue box with white lettering.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0565-2016·2016-02-17

    Celestial Seasonings Roastaroma Herbal Tea Recalled for Gluten Mislabeling

    Hain Celestial is recalling Roastaroma Herbal Tea because some packages are labeled 'Gluten Free' but contain barley.

    Product
    Celestial Seasonings Roastaroma Herbal Tea Lot code: Best Before 20DEC17 Pack size: 6 retail units (20 count)/ per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0768-2016·2016-02-17

    GE Healthcare Optima XR220amx Mobile Radiographic System Recalled for Safety Latch Failure

    GE Medical Systems is recalling 2,389 Optima XR220amx mobile radiographic systems worldwide due to a potential safety latch mechanism failure that could cause the arm assembly to fall.

    Product
    GE Healthcare, Optima XR220amx, Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0788-2016·2016-02-17

    Zimmer Biomet Recalls Endobon Xenograft Granules Due to Cytotoxicity Failure

    Biomet France SARL is recalling Endobon-Xenograft Granules because the product failed cytotoxicity tests at 36 months. Use past the 18-month shelf life may cause patient illness or injury.

    Product
    Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material, used in dental and/or surgical procedures. Endobon Xenograft Granules, Bone Grafting Material, Synthetic are used in the following dental and/or surgical procedures: " Alveolar ridge augmentation/recons
    Category
    Medical Device
    Distribution
    47 states
  • HighFDA (Devices)·Z-0797-2016·2016-02-17

    Orthofix Firebird Spinal Fixation System Torque Limiting Handle Recall

    Orthofix is recalling 36 Firebird Spinal Fixation System Torque Limiting Handles because they may deliver less torque than required after sterilization, potentially causing spinal construct loosening.

    Product
    Firebird Spinal Fixation System Torque Limiting Handle (PN 52-1512) Intended for posterior, non-cervical pedicle, and non-pedicle fixation (T1-S2/llium).
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0547-2016·2016-02-17

    Zzang! Cashew Cow Candy Bar Recalled for Undeclared Soy

    Zingerman's Candy Manufactory is recalling Zzang! Cashew Cow Candy Bars due to undeclared soy. The product was distributed in 18 states and DC.

    Product
    Zzang! Cashew Cow Candy Bar,2 oz., packaged in reprinted cardboard boxes, UPC 8 44397 00015 7
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·F-0559-2016·2016-02-17

    Signature Kitchens Hot Dog Buns Recalled for Foreign Material

    Albertsons is recalling Signature Kitchens Enriched Hot Dog Buns because cloth material from production equipment may be present in the product.

    Product
    Signature Kitchens Enriched Hot Dog; 8 buns; NET WT 12 oz 340 g UPC 0 21130 18501 6; Distributed by Living Better Brands, LLC, Pleasanton, CA 94566 Contains: Wheat May Contain eggs, milk.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0763-2016·2016-02-17

    GE Medical Systems Recalls Mavig Monitor Suspension System Due to Fall Risk

    GE Medical Systems is recalling 2,111 Mavig Monitor Suspension Systems because a reported incident involved a suspension arm falling to the floor.

    Product
    Mavig Monitor Suspension System, Model GD60, contained in the following Fluoroscopic imaging systems: Advantx LCV+, Advantx LCN+, Advantx LCLP+, Advantx LCA, INNOVA 2000, INNOVA 4100, INNOVA 3100, INNOVA 3131IQ, INNOVA 2121IQ, INNOVA 2100IQ, INNOVA 3100IQ, and INNOVA 4100IQ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0787-2016·2016-02-17

    DePuy SIGMA HP MBT Non-Keel Punch Knee Instrument Recalled

    DePuy Orthopaedics is recalling 351 SIGMA HP MBT Non-Keel Punch Knee Instruments due to a design defect that may cause surgical complications.

    Product
    SIGMA HP MBT Non-Keel Punch Knee Instrument. Designed to be used as an option in stabilizing the tibial trial during trial reduction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0374-2016·2016-02-17

    Kraft Singles American Recalled for Potential Choking Hazard

    The Kraft Heinz Company is recalling Kraft Singles American cheese slices because thin strips of packaging film may remain on the slices, posing a potential choking hazard.

    Product
    Kraft Singles American packaged in a blue box with white lettering.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0546-2016·2016-02-17

    Zzang! Original Candy Bar Recalled for Undeclared Soy and Milk

    Zingerman's Candy Manufactory is recalling Zzang! Original Candy Bars due to undeclared soy and milk allergens.

    Product
    Zzang! Original Candy Bar, 2.5 oz., packaged in preprinted cardboard boxes, UPC 8 44397 00014 0
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·F-0548-2016·2016-02-17

    Zingerman's Wowza Candy Bar Recalled for Undeclared Soy and Milk

    Zingerman's Candy Manufactory is recalling 1,499 Wowza Candy Bars due to undeclared soy and milk ingredients.

    Product
    Zzang! Wowza Candy Bar,3 oz., packaged in reprinted cardboard boxes, UPC 8 44397 00072 0
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·F-0549-2016·2016-02-17

    Zingerman's Candy Bars Recalled for Undeclared Soy and Milk Allergens

    Zingerman's Candy Manufactory is recalling Zzang! Holiday 4 pack Candy Bars due to undeclared soy and milk allergens.

    Product
    Zzang! Holiday 4 pack Candy Bars, 10.5 oz., packaged in preprinted cardboard boxes
    Category
    Food
    Distribution
    18 states
  • HighFDA (Drugs)·D-0655-2016·2016-02-17

    Fagron Recalls SyrSpend SF Grape Flavor Due to Yeast Contamination

    Fagron, Inc. is recalling SyrSpend SF Grape Flavor suspending base due to the presence of yeast. The recall affects 148 bottles distributed nationwide.

    Product
    SyrSpend SF, Suspending Base, Grape Flavored, a convenient, sweetened, sugar-free syrup-suspending vehicle specially formulated to assist in extemporaneous preparation of oral liquid dose forms, Rx Only, Shake Well, 4 L bottle, Manufactured by Fagron Inc., St. Paul, MN 55120, NDC
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0766-2016·2016-02-17

    Philips TraumaDiagnost X-ray Units Recalled for Arm Fall Hazard

    Philips is recalling TraumaDiagnost radiological examination units because the arm may not be fastened securely and could fall down.

    Product
    Philips Healthcare TraumaDiagnost; Codes: 72001, 720011, 720013, 720020; A radiological examination unit for emergency work and routine skeletal diagnosis.
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-0759-2016·2016-02-17

    Trumpf Medical Systems Recalls Patient Transport Shuttles Due to Tilting Hazard

    Trumpf Medical Systems is recalling 1,284 patient transport shuttles because the table top may tilt down quickly in the maximum Trendelenburg position.

    Product
    Patient transport Shuttle with Trendelenburg quick adjustment function (Jupiter, Mars, Titan, TruSystem and Saturn operating table systems). The shuttle is intended for the following applications: 1. Transfer, transport and storage of exchangeable table tops in the Trumpf Medica
    Category
    Medical Device
    Distribution
    2 states
  • HighCPSC·16104·2016-02-17

    Michaels Recalls Ashland Holiday Paper Boxes Due to Mold Risk

    Michaels is recalling Ashland holiday paper boxes because mold may be present, posing a risk of respiratory or other infections for consumers with compromised immune systems or mold allergies.

    Product
    Ashland® holiday paper boxes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0769-2016·2016-02-17

    GE Brivo XR285amx Mobile Radiographic System Recalled for Safety Latch Failure

    GE Medical Systems is recalling 126 Brivo XR285amx mobile radiographic systems worldwide because a safety latch mechanism may fail, posing a risk of bodily harm.

    Product
    GE Healthcare, Brivo XR285amx Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0770-2016·2016-02-17

    GE Healthcare Optima XR200amx Mobile Radiographic System Recalled for Safety Latch Failure

    GE Medical Systems is recalling 895 Optima XR200amx mobile radiographic systems worldwide due to a potential safety latch mechanism failure that could cause the arm assembly to fall.

    Product
    GE Healthcare, Optima XR200amx, Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0791-2016·2016-02-17

    Richard Wolf Reusable Rotary Blade Recalled for Weak Welds

    Richard Wolf Medical Instruments Corp. is recalling two reusable rotary blades due to weak welds that may cause the product to break during surgical use.

    Product
    Reuseable rotary blade/abrader, product number 899751514. The oval burr frontally hooded is an attachment or accessory to the air-powered device intended for use during surgical procedures to cut hard tissue or bone and soft tissue. General hospital and plastic surgery use.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0688-2016·2016-02-17

    Moog Recalls Curlin Infusion Pumps Due to Calibration Defect

    Moog is recalling specific Curlin infusion pumps because calibration errors may cause them to deliver medication faster than programmed.

    Product
    Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusion System includes Curlin Ambulatory multi-therapy and PainSmart pumps. Curlin 4000, catalog number 340; Curlin 6000, 6000 CMS, and PainSmart IOD, catalog number 360; and Curlin Pump Calibration Set, c
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0762-2016·2016-02-17

    Del Medical VS300 Radiographic Cassette Holder Recall for Falling Hazard

    Del Medical, Inc. is recalling VS300 radiographic cassette holders and wall stands because the unit can suddenly fall to the bottom of its travel and contact a patient.

    Product
    VS300 radiographic Cassette Holder or Wall Stand. For use in radiology department.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0790-2016·2016-02-17

    Richard Wolf Reusable Rotary Blade Recalled for Weak Welds

    Richard Wolf Medical Instruments Corp. is recalling four reusable rotary blade/abrader units due to weak welds that may cause the product to break during surgical use.

    Product
    Reuseable rotary blade/abrader, product number 899751504. The oval burr laterally hooded is an attachment or accessory to the air-powered device intended for use during surgical procedures to cut hard tissue or bone and soft tissue. General hospital and plastic surgery use.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-0558-2016·2016-02-17

    Signature Kitchens Crushed Wheat Hot Dog Buns Recalled for Foreign Material

    Albertsons Companies is recalling 184 packages of Signature Kitchens Crushed Wheat Hot Dog Buns because cloth material from production equipment may be present in the product.

    Product
    Signature Kitchens Crushed Wheat Hot Dog; 8 buns; NET WT 12 oz 340 g UPC 0 21130 18496 5; Distributed by Living Better Brands, LLC, Pleasanton, CA 94566 Contains: Wheat May Contain eggs, milk.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0654-2016·2016-02-17

    Fagron Recalls SyrSpend SF Syrup Due to Yeast Contamination

    Fagron, Inc. is recalling SyrSpend SF syrup-suspending vehicle due to the presence of yeast. The recall affects 44 bottles distributed nationwide.

    Product
    SyrSpend SF, a convenient, sweetened, sugar-free syrup-suspending vehicle specially formulated to assist in extemporaneous preparation of oral liquid dose forms, Rx Only, Shake Well, 500 mL bottle, Manufactured by Fagron Inc., St. Paul, MN 55120, NDC 51552-1079-5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0571-2016·2016-02-17

    Recall of CRIADA Green Pigeon Peas Due to Import Alert Status

    A.R. Food Brokerage Corp. is recalling CRIADA Green Pigeon Peas because the product was inadvertently released while under an FDA Import Alert.

    Product
    Label reading in part: "CRIADA***PREMIUM GANDULES VERDES GREEN PIGEON PEAS***In water with salt*** NET WT. 15 oz (425g)***Producido para/Produced for Empresas La Famosa, Inc.: P.O. Box 51968 Toa Baja, P.R. 00949***Product of Peru/Producto de Peru".
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0560-2016·2016-02-17

    Coast to Coast French Hoagie Rolls Recalled for Cloth Material Contamination

    Albertsons Companies is recalling Coast to Coast French Hoagie Rolls because cloth material from production equipment may be present in the product.

    Product
    Coast to Coast Parisian Style French 6 Hoagie Rolls; 6 Hoagie Rolls; NET WT 16.5 oz 468 g UPC 0 21130 18090 5; Distributed by Living Better Brands, LLC, Pleasanton, CA 94566 Contains: Wheat May Contain eggs, milk.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0661-2016·2016-02-17

    Safecor Health Recalls Haloperidol Oral Solution Due to Leaking Bottles

    Safecor Health is recalling 3,532 bottles of Haloperidol Oral Solution because customer complaints confirmed the bottles were leaking.

    Product
    Haloperidol Oral Solution, USP (Concentrate) 2 mg/mL 15 mL amber bottle, Rx Only, Manufactured by Silarx Pharmaceuticals Inc. Carmel, NY 10512, Packaged by Safecor Health, Woburn, MA 01801, NDC 54838-0501-40.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0657-2016·2016-02-17

    Safecor Recalls Midazolam Syrup Cups Due to Cardboard Contaminant

    Safecor Health is recalling specific lots of Midazolam HCl Syrup unit dose cups found to contain a small piece of cardboard.

    Product
    Midazolam HCl Syrup, 10 mg/5 mL, 5 mL unit dose cups, packaged in 2 shelf boxes, one shelf box containing 72 cups and one shelf box containing 60 cups, Cherry Brandy Flavor, Rx only, MFG: Roxane; PKG BY Safecor, Woburn, MA; Barcode 0054356605.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0656-2016·2016-02-17

    Fagron Recalls SyrSpend SF Suspending Base Due to Yeast Contamination

    Fagron, Inc. is recalling SyrSpend SF Suspending Base because the product contains yeast. The recall covers 88 bottles distributed nationwide.

    Product
    SyrSpend SF, Suspending Base, a convenient, sweetened, sugar-free syrup-suspending vehicle specially formulated to assist in extemporaneous preparation of oral liquid dose forms, Rx Only, Shake Well, 4 L bottle, Manufactured by Fagron Inc., St. Paul, MN 55120, NDC 51552-1079-9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0578-2016·2016-02-17

    Sunbest Natural Lemon Juice Recalled for Unapproved and Undeclared Color

    Sunco & Frenchie LLC is recalling Sunbest Natural Lemon Juice because it contains unapproved and undeclared color.

    Product
    Sunbest Natural Lemon Juice 33.5 Fl. Oz. Distributed by Sunco & Frenchie LLC Clifton, NJ 07011 UPC 089625403007
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0778-2016·2016-02-17

    Zimmer Dental Implants Recalled for Missing Safety Information in Instructions

    Zimmer Dental Inc is recalling specific dental implants because the instructions for use omitted safety information regarding the 3.7 mmD and 4.1 mmD Trabecular Metal models.

    Product
    IMPLANT,TM, MTX FULL 4.1 mm x 10 mm diameter 3.5 mm Catalog #TMT4B10 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one o
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0574-2016·2016-02-17

    Bearded Brothers BOLD The Greek Energy Bars Recalled for Mold

    Bearded Brothers LLC is recalling BOLD The Greek energy bars due to mold. The recall covers 150 cases distributed nationwide.

    Product
    Bearded Brothers BOLD The Greek Net Wt. 1.5 oz/43 g UPC: 8-50430-00414-2.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0794-2016·2016-02-17

    Merge Healthcare Recalls RadSuite Picture Archive System for Measurement Errors

    Merge Healthcare is recalling RadSuite picture archive systems because they may display incorrect Standardized Uptake Values (SUV). The recall covers 164 units distributed nationwide.

    Product
    RadSuite, a picture archive and communications system. Model Numbers Versions 5.30.0, 5.30.1, 5.30.2, 5.30.2 SB0344, 5.30.3, 5.30.4, 5.30.4 HF0418E, 5.30.5, 5.30.5 HF0404E, 5.30.5 HF0413E, 5.30.5 HF390E, 5.30.5 SB0368, 5.30.6, 5.30.6 HF0405E, 5.30.6 HF0406E, 5.30.7, 5.30.7 HF0429
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0785-2016·2016-02-17

    Bard Distaflo Vascular Bypass Graft Recalled for Size Mislabeling

    Bard Peripheral Vascular Inc is recalling four units of Bard Distaflo Vascular Bypass Grafts due to size mislabeling. The 8 mm grafts are incorrectly labeled as 6 mm.

    Product
    Bard Distaflo Vascular Bypass Graft; Product Code: DF6006SC; 8 mm x 60 cm. Intended for bypass or reconstruction of peripheral arterial blood vessels.
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0774-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was missing from the instructions for use.

    Product
    IMPLANT,TM, MTX 4.1 mm x 13 mm diameter 3.5 mm Catalog #TMM4B13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or mor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0786-2016·2016-02-17

    Bard Distaflo Vascular Bypass Graft Recalled for Size Mislabeling

    Bard Peripheral Vascular Inc is recalling four units of the Bard Distaflo Vascular Bypass Graft because the product is mislabeled as 6 mm when it is actually 8 mm.

    Product
    Bard Distaflo Vascular Bypass Graft; Product Code: DF8006SC; 6 mm x 80 cm. Intended for bypass or reconstruction of peripheral arterial blood vessels.
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Food)·F-0577-2016·2016-02-17

    Bulletproof Recalls Tangerine FATwater Bottles Due to Microbial Growth

    Bulletproof Digital Inc is recalling 5,748 bottles of Tangerine FATwater due to microbial growth detection. No pathogens were detected.

    Product
    FATwater bottle, 16.9 fl. oz., Tangerine flavor, UPC 6 41871 93693 9
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0772-2016·2016-02-17

    Zimmer Dental Implants Recalled for Missing Instructions

    Zimmer Dental Inc. is recalling specific dental implants because the latest instructions omitted information for certain models.

    Product
    IMPLANT,TM, MTX 4.1 mm x 10 mm diameter 3.5 mm Catalog #TMM4B10 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or mor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0568-2016·2016-02-17

    Thai Green Curry Sauce Recalled Due to Potential Mold Presence

    Thai Culinary Arts Studio LLC is recalling Watcharee's Thai Green Curry Sauce because it may contain mold and fail quality standards.

    Product
    Watcharee's Thai Green Curry Sauce (UPC 094368999991), product is in a glass jar, NET WT 11.5 OZ (326 g)
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0758-2016·2016-02-17

    Spectranetics Recalls Expired 2.3mm Turbo-Power Laser Atherectomy Catheters

    Spectranetics Corp. is recalling 8 units of 2.3mm Turbo-Power OTW Manual laser atherectomy catheters because they are past their expiration date.

    Product
    2.3mm Turbo-Power OTW, Manual, Model No 423-050 Product Usage The Turbo-Power System (Laser Atherectomy Catheter) is a laser atherectomy device designed for use with the CVX-300" Excimer Laser System. The Turbo-Power Laser Atherectomy Catheter is a sterile, single use, prescript
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0795-2016·2016-02-17

    PharmaCaribe PulmoSal 7% Sodium Chloride Inhalation Solution Recalled for Mislabeling

    Pharmacaribe LLC is recalling PulmoSal 7% Sodium Chloride inhalation solution because vials were labeled as USP 7% Hypertonic saline instead of PulmoSal 7% (pH+).

    Product
    PharmaCaribe PulmoSal 7% Sodium chloride, Inhalation Solution, 7% Sterile, Preservative -free, Non-pyrogenic, pH 7.4 For Inhalation Only Rx Product Usage: The contents of these vials are used in conjunction with a nebulizer for the induction of sputum production where sputu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0555-2016·2016-02-17

    Albertsons Recalls Pantry Essentials Hamburger Buns Due to Foreign Material

    Albertsons Companies is recalling Pantry Essentials Hamburger Buns because cloth material from production equipment may be present in the product.

    Product
    Pantry Essentials Hamburger Buns; 8 buns; NET WT 12 oz 340 g UPC 0 21130 27085 9; Distributed for: Lucerne Foods Inc. Pleasanton, CA 94566 Contains: Wheat May Contain eggs, milk.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0783-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc is recalling specific Trabecular Metal dental implants because safety information was missing from the instructions for use.

    Product
    IMPLANT,TM, MTX FULL 3.7 mm x 13 mm diameter 3.5 mm Catalog #TMTB13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0575-2016·2016-02-17

    Bulletproof Recalls Berry FATwater Bottles Due to Microbial Growth

    Bulletproof Digital Inc is recalling 12,583 bottles of Berry FATwater due to microbial growth detection. No pathogens were detected.

    Product
    FATwater bottle, 16.9 fl. oz., Berry flavor, UPC 6 09015 50477 2
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0566-2016·2016-02-17

    Thai Culinary Arts Studio Recalls Thai Peanut Sauce Due to Mold

    Thai Culinary Arts Studio LLC is recalling 4,327 jars of WATCHAREE'S thai peanut sauce because the product may contain mold.

    Product
    WATCHAREE'S thai peanut sauce (UPC 094368999977), product is in a glass jar, NET WT 11.75 OZ (333 g)
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0781-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc. is recalling specific Trabecular Metal implants because safety information was omitted from the instructions for use.

    Product
    IMPLANT,TM, MTX FULL 3.7 mm x 10 mm diameter 3.5 mm Catalog #TMTB10 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0563-2016·2016-02-17

    Albertsons Recalls White Diner Rolls Due to Potential Cloth Contamination

    Albertsons Companies, Inc. is recalling Old Fashioned White Diner Rolls because cloth material from production equipment may be present in the product.

    Product
    Old Fashioned White Diner Rolls 8 Count Pack size 20 oz. UPC 2 24246 00000
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0779-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was omitted from the latest instructions for use.

    Product
    IMPLANT,TM, MTX FULL 4.1 mm x 11.5 mm diameter 3.5 mm Catalog #TMT4B11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0552-2016·2016-02-17

    Open Nature Seeded Sandwich Rolls Recalled for Foreign Material

    Albertsons is recalling Open Nature Seeded Sandwich Rolls because cloth material from production equipment may be present in the product.

    Product
    Open Nature Seeded Sandwich Rolls; 8 buns; NET WT 21 oz (1 lb 5 oz) 595 g UPC 0 79893 11439 2; Distributed by: Lucerne Foods, inc. Pleasanton, CA 94566 Contains: Wheat May Contain egg, milk.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-0553-2016·2016-02-17

    Safeway Kitchens Hamburger Buns Recalled for Potential Cloth Material Contamination

    Albertsons Companies is recalling Safeway Kitchens Enriched Hamburger Buns because cloth material from production equipment may be present in the product.

    Product
    Safeway Kitchens Enriched Hamburger Buns; 8 buns; NET WT 17 oz (1 lb 1 oz) 482 g UPC 0 21130 18456 9; Distributed by:Safeway Inc. Pleasanton, CA 94566 Contains: Wheat May Contain eggs, milk.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0776-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc is recalling specific dental implants because safety information was omitted from the instructions for use.

    Product
    IMPLANT,TM, MTX 3.7 mm x 11.5 mm diameter 3.5 mm Catalog #TMMB11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or mo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0780-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc is recalling specific Trabecular Metal dental implants because safety information was omitted from the instructions for use.

    Product
    IMPLANT,TM, MTX FULL 4.1 mm x 13 mm diameter 3.5 mm Catalog #TMT4B13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one o
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0572-2016·2016-02-17

    A.R. Food Brokerage Recalls Green Pigeon Peas Due to Import Alert

    A.R. Food Brokerage Corp. is recalling 15-ounce cans of Green Pigeon Peas because the product was inadvertently released for distribution while under an FDA Import Alert.

    Product
    Label reading in part: "ECONO***Gandules Verde***Hervidos en Agua y Sal*** Green Pigeon Peas***PREMIUM***NET WT. 15 oz (425g)***PRODUCTO DE PERU***EMPACADO PARA: SUPERMERCADOS ECONO, INC. Carolina, P.R. 00984".
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0659-2016·2016-02-17

    Sandoz Recalls Candesartan Cilexetil Tablets Due to Impurity Failures

    Sandoz Inc. is recalling Candesartan Cilexetil Tablets, 16 mg, because the product failed impurities and degradation specifications at a 9-month stability timepoint.

    Product
    Candesartan Cilexetil Tablets, 16 mg, a) 30 count (NDC 00781-5938-31) and b) 90 count (NDC 00781-5938-92) bottles, Rx Only, Manufactured by Mylan Laboratories Limited Hyderabad 500 034, India for Sandoz Inc. Princeton, NJ 08540
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0554-2016·2016-02-17

    Albertsons Recalls Pantry Essentials Hot Dog Buns Due to Foreign Material

    Albertsons Companies, Inc. is recalling Pantry Essentials Hot Dog Buns because cloth material from production equipment may be present in the product.

    Product
    Pantry Essentials Hot Dog Buns; 8 buns; NET WT 12 oz 340 g UPC 0 21130 27084 2; Distributed for: Lucerne Foods Inc. Pleasanton, CA 94566 Contains: Wheat May Contain eggs, milk.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0775-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Instructions in Manual

    Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because critical safety information was missing from the instruction manual.

    Product
    IMPLANT,TM, MTX 3.7 mm x 10 mm diameter 3.5 mm Catalog #TMMB10 Product Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or more missing
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0796-2016·2016-02-17

    Salter Labs Recalls T-piece Nebulizers Due to Fit Issues

    Salter Labs is recalling 70 T-piece Nebulizers because the T-piece does not fit on the nebulizer. The devices were distributed in six US states and China.

    Product
    T-piece Nebulizer with in-line connectors, Part number 8915-7-50. Single patient use, non-sterile prescription device designed for use in a hospital or home care environment.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·F-0576-2016·2016-02-17

    Bulletproof FATwater Lemon Bottles Recalled for Microbial Growth

    Bulletproof Digital Inc is recalling FATwater Lemon bottles due to microbial growth detection. No pathogens were found.

    Product
    FATwater bottle, 16.9 fl. oz., Lemon flavor, UPC 6 09015 50475 8
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0567-2016·2016-02-17

    Thai Massaman Curry Sauce Recalled for Potential Mold Presence

    Thai Culinary Arts Studio LLC is recalling WATCHAREE'S Thai Massaman curry sauce because the product may contain mold.

    Product
    WATCHAREE'S Thai Massaman curry sauce (UPC 094368999984), product is in a glass jar, NET WT 11.5 OZ (326 g)
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-0573-2016·2016-02-17

    Bearded Brothers BOLD Coconut Curry Energy Bars Recalled for Mold

    Bearded Brothers LLC is recalling 128 cases of BOLD Coconut Curry energy bars due to mold. The product was distributed nationwide.

    Product
    Bearded Brothers BOLD Coconut Curry Net Wt. 1.5 oz/43 g UPC: 8-50430-00513-5.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0556-2016·2016-02-17

    Signature Kitchens Whole Wheat Hot Dog Buns Recalled for Cloth Material

    Albertsons Companies is recalling Signature Kitchens 100% Whole Wheat Hot Dog Buns because cloth material from production equipment may be present in the product.

    Product
    Signature Kitchens 100% Whole Wheat Hot Dog Buns; 8 buns; NET WT 16 oz 454 g UPC 0 21130 15456 2; Distributed by Living Better Brands, LLC, Pleasanton, CA 94566 Contains: Wheat May Contain eggs, milk.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-0564-2016·2016-02-17

    Albertsons Recalls Wheat Diner Rolls for Potential Cloth Contamination

    Albertsons Companies is recalling Old Fashioned Wheat Diner Rolls because cloth material from production equipment may be present in the product.

    Product
    Old Fashioned Wheat Diner Rolls 8 Count Pack size 20 oz. UPC 2 24247 00000
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0752-2016·2016-02-17

    Toshiba INFX-8000V X-Ray System Recalled for Dose Meter Error

    Toshiba is recalling four INFX-8000V Bi-Plane X-Ray Interventional Systems because a software error caused dose data to be lost during specific imaging procedures.

    Product
    INFX-8000V Bi-Plane X-Ray Interventional System X-ray systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0562-2016·2016-02-17

    Albertsons Recalls Hawaiian Dinner Rolls Due to Foreign Material

    Albertsons Companies is recalling Coast to Coast Hawaiian Dinner Rolls because cloth material from production equipment may be present in the product.

    Product
    Coast to Coast Traditional Hawaiian Sweet 12 Dinner Rolls; 12 Dinner Rolls; NET WT 14 oz 397 g UPC 0 21130 18580 1; Distributed by Living Better Brands, LLC, Pleasanton, CA 94566 Contains: Wheat. milk May Contain eggs
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-0551-2016·2016-02-17

    Albertsons Recalls Open Nature Hot Dog Buns Due to Foreign Material

    Albertsons is recalling Open Nature Whole Grain White Hot Dog Buns because cloth material from production equipment may be present in the product.

    Product
    Open Nature Whole Grain White Hot Dog Buns; 8 buns; NET WT 12 oz (340 g) UPC 0 79893 11057 8; Distributed by: Lucerne Foods, inc. Pleasanton, CA 94566 Contains: Wheat, milk May Contain egg, milk.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0773-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was omitted from the instructions for use.

    Product
    IMPLANT,TM, MTX 4.1 mm x 11.5 mm diameter 3.5 mm Catalog #TMM4B11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or m
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0557-2016·2016-02-17

    Signature Kitchens Hamburger Buns Recalled for Potential Cloth Contamination

    Albertsons is recalling Signature Kitchens Enriched Hamburger Buns because cloth material from production equipment may be in the product.

    Product
    Signature Kitchens Enriched Hamburger Buns, Sesame; 8 buns; NET WT 12 oz 340 g UPC 0 21130 18467 5; Distributed by Living Better Brands, LLC, Pleasanton, CA 94566 Contains: Wheat May Contain eggs, milk.
    Category
    Food
    Distribution
    3 states
  • LowFDA (Devices)·Z-0782-2016·2016-02-17

    Zimmer Dental Implants Recalled for Missing Instructions in Manual

    Zimmer Dental Inc is recalling specific Trabecular Metal implants because the latest instruction manual omitted critical safety information for certain sizes.

    Product
    IMPLANT,TM, MTX FULL 3.7 mm x 11.5 mm diameter 3.5 mm Catalog #TMTB11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0660-2016·2016-02-17

    Amerisource Recalls Candesartan Cilexetil Tablets Due to Impurity Failures

    Amerisource Health Services is recalling 716 cartons of Candesartan Cilexetil Tablets, 16 mg, due to failed impurities and degradation specifications.

    Product
    Candesartan Cilexetil Tablets, 16 mg, 30 Tablets (5 x 6) blister pack, Rx, Distributed by: American Health Packaging Columbus, Ohio 43217, NDC 68084-877-25(carton), NDC 68084-877-95(individual dose)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0784-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc. is recalling specific dental implants because safety information was missing from the instructions for use.

    Product
    IMPLANT,TM, MTX FULL 3.7 mm x 16 mm diameter 3.5 mm Catalog #TMTB16 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0777-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Instructions

    Zimmer Dental Inc. is recalling specific dental implants because important safety information was missing from the latest instruction manual.

    Product
    IMPLANT,TM, MTX 3.7 mm x 13 mm diameter 3.5 mm Catalog #TMMB13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or more
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V086000·2016-02-16

    Starcraft AR-One Toy Hauler Recall for Incorrect Tire Labels

    Starcraft is recalling 2016 AR-One toy hauler trailers because incorrect tire labels may lead to improper tire replacement, increasing crash risk.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AR-ONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V088000·2016-02-16

    IMT Recalls Dominator Cranes Due to Valve Bank Cover Defect

    Iowa Mold Tooling is recalling 2013-2016 Dominator vehicles because a valve bank cover may crack and fall off, creating a road hazard.

    Product
    IMT — IMT DOMINATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V087000·2016-02-16

    Mercedes-Benz Recalls 2016 C300 and C450 Models for Sunroof Defect

    Mercedes-Benz is recalling specific 2016 C300 and C450 vehicles because the panoramic sunroof glass may not be properly bonded and could detach during operation.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C300, C450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·018-2016·2016-02-16

    Winter Gardens Recalls Chicken Salad Due to Plastic Contamination

    Winter Gardens Quality Foods is recalling approximately 3,710 pounds of Southwest Chicken Salad due to possible contamination with extraneous plastic materials.

    Product
    Sandridge - PA, LLC — Winter Gardens Quality Foods, Inc. Recalls Chicken Salad Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·017-2016·2016-02-13

    Canyon Creek Soup Co. Recalls Uninspected Vietnamese Beef Meatball Soup Kits

    Canyon Creek Soup Co. is recalling approximately 7,275 pounds of beef meatball soup kits that were imported without U.S. inspection. The products were shipped to retail outlets in California.

    Product
    Canyon Creek Soup Co. Recalls Beef Products Produced Without Benefit Of Import Inspection
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·016-2016·2016-02-12

    McCain Recalls Bacon Fritters Due To Possible Plastic Contamination

    McCain Foods USA is recalling approximately 25,215 pounds of potato, egg, cheese, and bacon fritters that may contain extraneous plastic materials.

    Product
    McCain Foods USA, Inc. — McCain Foods USA, Inc. Recalls Pork Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    12 states
  • SevereNHTSA·16V085000·2016-02-12

    Trans Tech Student Safety Transporter School Bus Barrier Recall

    Transportation Collaborative is recalling 2012-2015 Trans Tech Student Safety Transporter school buses because the driver's side barrier may not deform properly in a crash.

    Product
    TRANS TECH BUS — TRANS TECH BUS STUDENT SAFETY TRANSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16101·2016-02-12

    Crescent Point Energy Recalls Propane Gas Due to Fire and Burn Hazards

    Crescent Point Energy is recalling approximately 118 million gallons of propane gas in the U.S. because insufficient odorant levels may prevent consumers from detecting leaks, posing fire and burn risks.

    Product
    Propane (LP) Gas
    Category
    Consumer Product
    Distribution
    Distributed nationwide

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