The Recall Desk

Archive

April 2016 recalls

764 recalls were announced in April 2016.

What the numbers show

Critical
20
Severe
108
High
373
Moderate
207
Low
56

Of the 764 recalls this month scored against our rubric, 3% are Critical, 14% are Severe.

1–100 of 764

  • SevereNHTSA·16V260000·2016-04-29

    Thor Motor Coach Recalls 2017 ACE and Road Bear Rental Motorhomes

    Thor Motor Coach is recalling 2017 ACE and Road Bear Rental motorhomes because seat belt anchorages in the slide-out section may pull loose during a crash.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH ROAD BEAR RENTAL, ACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·033-2016·2016-04-29

    Foster Farms Recalls Frozen Chicken Nuggets Due to Foreign Materials

    Foster Farms is recalling approximately 220,450 pounds of frozen chicken nuggets that may contain blue plastic and black rubber.

    Product
    Case Farms, Processing — Foster Poultry Farms Recalls Poultry Products Due To Possible Foreign Materials Contamination
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·16V261000·2016-04-29

    Mercedes-Benz and Freightliner Sprinter Vans Recalled for Window Separation Risk

    Daimler Vans USA is recalling 2015-2016 Mercedes-Benz and Freightliner Sprinter vans because multiple paint layers may cause windows to separate in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·032-2016·2016-04-29

    Greencore USA Recalls Meat and Poultry Products Produced Without Inspection

    Greencore USA is recalling approximately 1,341 pounds of meat and poultry wraps and salads produced without federal inspection. No adverse reactions have been reported.

    Product
    Greencore USA Recalls Meat, Poultry Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    7 states
  • HighNHTSA·16C005000·2016-04-29

    Kiddy USA Recalls World Plus Child Seats Due to Buckle Defect

    Kiddy USA is recalling World Plus child seats because the harness buckle may not fully latch, increasing injury risk in a crash.

    Product
    CHILD SEAT:HARNESS/CROTCH BUCKLE recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V258000·2016-04-29

    Forest River Cardinal RVs Recalled for Incorrect Tire Placard Information

    Forest River is recalling 2016-2017 Cardinal RVs because the tire placard lists incorrect tire and rim specifications, which could lead to under-inflation and tire blowouts.

    Product
    FOREST RIVER — FOREST RIVER CARDINAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V259000·2016-04-29

    Monroe Truck Equipment Recalls 2013 Ford F-550 Trucks with IMT Cranes

    Monroe Truck Equipment is recalling one 2013 Ford F-550 truck equipped with an IMT crane because the valve bank cover may crack and fall off, creating a road hazard.

    Product
    MONROE — MONROE FORD F-550 W/IMT CRANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V252000·2016-04-28

    Newmar Recalls 2014-2016 Motorhomes Due to Brake Signal Defect

    Newmar is recalling 1,150 recreational vehicles because the brake signal to towed devices may not deactivate, causing dragging brakes, overheating, or fire.

    Product
    NEWMAR — NEWMAR LONDON AIRE, ESSEX, MOUNTAIN AIRE, DUTCH STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V256000·2016-04-28

    GM Recalls 2016-2017 Trucks and SUVs for Front Control Arm Weld Defect

    General Motors is recalling specific 2016-2017 Chevrolet, GMC, and Cadillac vehicles because inadequate welds on the front upper control arms may separate, compromising steering and increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC SILVERADO 1500, SIERRA 1500, TAHOE, YUKON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V255000·2016-04-28

    Legacy Equipment Recalls Dominator Trucks Due to Crane Cover Defect

    Legacy Equipment is recalling 2013-2016 Dominator trucks because a crane valve bank cover may crack and fall off, creating a road hazard.

    Product
    LEGACY EQUIPMENT — LEGACY EQUIPMENT DOMINATOR I, DOMINATOR II, DOMINATOR III, DOMINATOR IV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V253000·2016-04-28

    RAM ProMaster Recall for Trailer Brake Light Software Error

    Chrysler is recalling 2014-2016 RAM ProMaster and 2015-2016 ProMaster City vehicles because a software error may prevent trailer brake lights from illuminating, increasing crash risk.

    Product
    RAM — RAM PROMASTER, PROMASTER CITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V254000·2016-04-28

    Custom Truck Recalls Dominator Trucks with IMT Crane Valve Cover Defect

    Custom Truck is recalling 2013-2016 Dominator trucks equipped with specific IMT cranes because the valve bank cover may crack and fall off, creating a road hazard.

    Product
    CUSTOM TRUCK — CUSTOM TRUCK DOMINATOR I, DOMINATOR-PROPANE, DOMINATOR IV, DOMINATOR III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E039000·2016-04-28

    RAM ProMaster Trailer Light Module Recall for Brake Light Failure

    Chrysler is recalling RAM ProMaster Trailer Light Modules due to a software error that can prevent trailer brake lights from illuminating, increasing crash risk.

    Product
    RAM — RAM PROMASTER, PROMASTER CITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·16V257000·2016-04-28

    GM Recalls 2013-2016 Chevrolet Vehicles for Theft Protection Software Defect

    General Motors is recalling certain 2013-2016 Chevrolet Sonic, Trax, and Spark vehicles because the radio software may fail to provide an audible warning chime, increasing the risk of vehicle theft.

    Product
    CHEVROLET — CHEVROLET TRAX, SPARK, SONIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1099-2016·2016-04-27

    Ricotta Cheese Recalled for Listeria monocytogenes Contamination

    Delicious Food Distributors Inc is recalling 47 tubs of 33 Kopobbi A Whole Milk Cheese Ricotta due to Listeria monocytogenes contamination.

    Product
    33 Kopobbi A WHOLE MILK CHEESE, Ricotta, Net Weight: 17.14 lb.
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-1121-2016·2016-04-27

    Shakti Group Recalls Asafoetida Powder for Potential Salmonella Contamination

    Shakti Group USA LLC is recalling approximately 10,000 bottles of L.G. Compounded Asafoetida Powder due to potential Salmonella contamination. The product was distributed in New Hampshire, New Jersey, Pennsylvania, Ohio, and Virginia.

    Product
    1) COMPOUNDED ASAFOETIDA POWDER L.G.¿, NET WT. 50g (1.75OZ.), MANUFACTURED BY: LALJEE GODHOO & CO. 213, Samuel Street, Mumbai - 400 003, (INDIA) MANUFACTURED AT: LALJEE GODHOO & CO. Plot No. 53/4, Road 7/15, M.I.D.C.,Andheri (E). Mumbai - 400 093. (INDIA) Lot No., Pkd & Best Be
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1085-2016·2016-04-27

    Thomas Produce Recalls Cucumbers Contaminated with Salmonella

    Thomas Produce Co. is recalling cucumbers contaminated with Salmonella. The affected produce was distributed to firms in Florida and Georgia.

    Product
    Cucumbers packed in 1 1/9 cardboard bushel boxes (~55-lb) and 1000-lb cardboard bins. Refrigerate at 40-60 degF. Pick date of 12/15/2015.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Devices)·Z-1529-2016·2016-04-27

    Mevion S250 Proton Therapy System Recalled for Gantry Motion Hazard

    Mevion Medical Systems is recalling five MEVION S250 proton therapy systems because an aperture may fall out during gantry motion, posing a risk of traumatic injury or death to patients.

    Product
    MEVION S250 for Proton Radiation Therapy
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1092-2016·2016-04-27

    Peru Food Mote Corn Recalled for Undeclared Sulfites

    Peru Food Import Inc. is recalling 2,664 bags of Mote Corn Maiz Mote due to undeclared sulfites. The product was distributed in New York and Connecticut.

    Product
    Peru Food Mote Corn Maiz Mote Net Wt. 15 oz. Imported and distributed by: Peru Food Import Inc.PO Box 419 West New York, NJ 07093 UPC 812125009628
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0829-2016·2016-04-27

    Hospira Recalls Dextrose Injection Bags Due to Chemical Contamination Risk

    Hospira Inc. is recalling 552 bags of Dextrose Injection, USP, 20% due to potential contamination with an aromatic hydrocarbon resin.

    Product
    Dextrose Injection, USP, 20%, Packaged as 500 mL in 1000 mL Bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7935-19, Barcode (01) 0 030409 793519 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V249000·2016-04-27

    2016 Jeep Grand Cherokee Recall for Brake Shift Interlock Defect

    Chrysler is recalling 2016 Jeep Grand Cherokee vehicles because a loose electrical connection in the brake transmission shift interlock solenoid may cause the transmission to lock in Park or Neutral.

    Product
    JEEP — JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1097-2016·2016-04-27

    Chicago Kimchee Recalls Korea White Kimchee for Undeclared Anchovies

    Chicago Kimchee is recalling Korea white Kimchee because it contains undeclared anchovies. Consumers with this product should stop using it.

    Product
    Korea white Kimchee packaged in 1 gallon, 1/2 gallon, packaged in glass jars inside plastic containers with multi colored label and black lettering.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1082-2016·2016-04-27

    Brian's Cauliflower Recalled for Undeclared Sulfites

    European Natural Foods & Trading Company is recalling Brian's Cauliflower 83 oz jars due to undeclared sulfites. The product was distributed in Connecticut, Massachusetts, New Jersey, and New York.

    Product
    Brians Cauliflower 83 oz Imported by EUROPEAN NATURAL FOOD & TRADING CO. Inc, 72 Lehigh Avenue Paterson, NJ 07593 UPC 858567002421
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0825-2016·2016-04-27

    Impax Recalls Dextroamphetamine Sulfate Tablets Due to Failed Impurity Specifications

    Impax Laboratories is recalling 67,428 bottles of Dextroamphetamine Sulfate Tablets USP, 10 mg, because the product failed impurities and degradation specifications.

    Product
    Dextroamphetamine Sulfate Tablets USP, 10 mg, 100-count bottle, Rx only, Manufactured and Distributed by: Corepharma, LLC, Middlesex, NJ 08846, NDC 64720-0216-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1098-2016·2016-04-27

    Chicago Kimchee Recalls Kimchee for Undeclared Anchovies

    Chicago Kimchee is recalling 1-gallon jars of Korea whole Kimchee due to undeclared anchovies, a major food allergen.

    Product
    Korea whole Kimchee packaged in 1 gallon packaged in glass jars inside plastic containers with multi colored label and black lettering.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1123-2016·2016-04-27

    Native Catch Salmon Bacon Recalled for Potential Botulism Contamination

    Swinomish Fish Company is recalling Native Catch Salmon Bacon due to potential Clostridium botulinum contamination discovered during a routine inspection.

    Product
    Native Catch Salmon Bacon, Traditional flavor. UPC 7 83583 27965 9. Traditional Salmon Bacon is ground and seasoned skinless/boneless salmon, extruded, peppered, smoked, cooled and vacuum packed in 8 oz., 14 oz., and 5 lbs. clear vacuum bags. Label states keep refrigerated
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1088-2016·2016-04-27

    Bimbo and Sara Lee Whole Wheat Bread Recalled for Glass Contamination

    BIMBO Bakeries USA Inc. is recalling multiple brands of 100% Whole Wheat Bread due to possible glass contamination. Consumers should check their bread bags for the specific UPCs and dates listed.

    Product
    Bimbo 100% Whole Wheat Bread, 16oz, On bag: SEP 01, UPC: 7432309230 Sara Lee 100% Whole Wheat Bread 16 oz On bag: SEP 01 UPC: 7294561103; Sara Lee 100% Whole Wheat Bread 20 oz On bag: SEP 01 UPC: 7294560134; Kroger 100% Whole Wheat Round Top Bread, 16 oz, On ba
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-1530-2016·2016-04-27

    Acorn 180 Curved Stairlift Recalled Due to Broken Rivets

    Acorn Stairlifts Inc is recalling 1,290 Acorn 180 Curved Stairlifts in the US because aluminum rivets may break under prolonged use.

    Product
    Acorn 180 Curved Stairlift
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1124-2016·2016-04-27

    Native Catch Salmon Bacon Recalled for Potential Botulism Risk

    Swinomish Fish Company is recalling Native Catch Salmon Bacon, Peppered flavor, due to potential Clostridium botulinum contamination discovered during a routine inspection.

    Product
    Native Catch Salmon Bacon, Peppered flavor. UPC: 7 51778 15900 0. Peppered Salmon Bacon is ground and seasoned skinless/boneless salmon, extruded, peppered, smoked, cooled and vacuum packed in 8 oz., 14 oz. and 5 lbs. clear vacuum bags. Label states keep refrigerated or fro
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0828-2016·2016-04-27

    Hospira Recalls Dextrose Injection Bags Due to Chemical Contamination

    Hospira Inc. is recalling 4,368 bags of Dextrose Injection, USP, 50% due to potential contamination with an aromatic hydrocarbon resin.

    Product
    Dextrose Injection, USP, 50%, Packaged as 500 mL in 1000 mL Bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7936-19, Barcode (01) 0 030409 793619 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0826-2016·2016-04-27

    Impax Recalls Dextroamphetamine Sulfate Tablets Due to Failed Impurity Specifications

    Impax Laboratories is recalling specific lots of Dextroamphetamine Sulfate Tablets because they failed impurity and degradation specifications.

    Product
    Dextroamphetamine Sulfate Tablets USP, 5 mg, 100-count bottle, Rx only, Manufactured and Distributed by: CorePharma, LLC, Middlesex, NJ 08846, NDC 64720-215-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V248000·2016-04-27

    Ford Recalls 2011-2012 F-150, Mustang, Expedition, Navigator for Transmission Defect

    Ford is recalling specific 2011-2012 F-150, Mustang, Expedition, and Navigator vehicles because the automatic transmission may unexpectedly downshift to first gear, increasing crash risk.

    Product
    FORD — FORD, LINCOLN F-150, MUSTANG, EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1551-2016·2016-04-27

    Smith & Nephew Recalls TC-PLUS Knee Prosthesis Due to Dimensional Deviation

    Smith & Nephew is recalling 6 units of TC-PLUS tibial knee prostheses due to a dimensional deviation that may prevent the polyethylene insert from seating correctly during surgery.

    Product
    TC-PLUS(TM), Primary Fixed Tibial Component VKS Right, SIZE 12 RIGHT, STERILE R, REF 12 000 028, S&N 7500283, Smith & Nephew Orthopaedics AG Product Usage: Tibial knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0832-2016·2016-04-27

    Hospira Recalls Potassium Chloride Injection Bags Due to Chemical Contamination

    Hospira Inc. is recalling 81,888 bags of Potassium Chloride Injection due to potential contamination with an aromatic hydrocarbon resin.

    Product
    Potassium Chloride Injection 20 mEq, 400 mEq/L, Packaged in 50 mL Bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7077-14
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1521-2016·2016-04-27

    Siemens CT Systems Recalled for Software Bugs Causing Scan Aborts

    Siemens Medical Solutions is recalling 1,096 CT systems due to software bugs that may cause scan aborts, rescans, or accidental x-radiation.

    Product
    Siemens SOMATOM Definition, SOMATOM Definition AS, SOMATOM Definition Flash and SOMATOM Definition Edge; Intended to produce cross-sectional images of the body. Computed tomography (CT) x-ray system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1547-2016·2016-04-27

    Smith & Nephew Recalls TC-PLUS Tibial Knee Prosthesis Components

    Smith & Nephew is recalling 33 units of TC-PLUS tibial knee prosthesis components due to a dimensional deviation that may prevent proper seating of the polyethylene insert during surgery.

    Product
    TC-PLUS(TM), Primary Fixed Tibial Component VKS Right, SIZE 4 RIGHT, STERILE R, REF 12 000 024, S&N 7500279, Smith & Nephew Orthopaedics AG Product Usage: Tibial knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1504-2016·2016-04-27

    Philips AutoSPECT Pro Software Recalled for Incorrect Cardiac Image Reconstruction

    Philips Medical Systems is recalling the AutoSPECT Pro software application because it may produce erroneous results when processing cardiac SPECT data acquired at detector angles other than 90 or 180 degrees.

    Product
    Extended Brilliance Workspace NM Nuclear medicine image display and processing application suite. AutoSPECT Pro Software Application. Philips Medical Systems, Cleveland, OH. Provides software applications used to process, analyze, and display medical images/data.
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Food)·F-1084-2016·2016-04-27

    Specialty Commodities Recalls Dry Roasted Almonds Due to Undeclared Cashews

    Specialty Commodities, Inc. is recalling dry roasted almonds because cashews were mixed with the product but the cashew allergen was not declared on the packaging.

    Product
    Almonds, dry roasted, not salted, packaged in 25 lb. cardboard cartons
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1008-2016·2016-04-27

    True Nature Original Hummus Recalled for Undeclared Soy

    True Nature LLC is recalling Original Hummus 9oz containers due to undeclared soy from the ingredient Tamari. The recall affects 464 units sold in Oregon and Washington.

    Product
    Original Hummus 9oz container
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1087-2016·2016-04-27

    Sara Lee Multi-Grain Bread Recalled for Possible Glass Contamination

    BIMBO Bakeries USA Inc. is recalling specific Sara Lee Delightful Healthy Multi-Grain Bread products due to possible glass contamination.

    Product
    Sara Lee Delightful Healthy Multi-Grain Bread Twin pack, 2 lbs 8 oz, On bag: AUG 29, UPC: 7294561169; Sara Lee Delightful Healthy Multi-Grain Bread, 20 oz, On bag: SEP 01, UPC: 7294571588
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-1089-2016·2016-04-27

    Bimbo Bakeries Recalls Fit & Active Multigrain Bread for Glass Contamination

    BIMBO Bakeries USA Inc. is recalling 2,080 bags of Fit & Active Multigrain Bread due to possible glass contamination. The product was distributed across ten southeastern and mid-Atlantic states.

    Product
    Fit & Active Multigrain Bread, 20 oz, On bag: AUG 31, UPC: 4149821093
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-1550-2016·2016-04-27

    Smith & Nephew Recalls TC-Plus Knee Prosthesis Due to Dimensional Deviation

    Smith & Nephew is recalling specific TC-Plus knee prostheses distributed in Germany and Switzerland because a dimensional deviation may prevent the polyethylene insert from seating correctly during surgery.

    Product
    TC-PLUS(TM), Primary Fixed Tibial Component VKS Right, SIZE 10 RIGHT, STERILE R, REF 12 000 027, S&N 7500282, Smith & Nephew Orthopaedics AG Product Usage: Tibial knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1525-2016·2016-04-27

    Coloplast Recalls Pediatric Catheters Due to Missing Eyelets

    Coloplast is voluntarily recalling a single lot of Self-Cath Pediatric Catheters because some units have missing eyelets, which can cause catheter malfunction.

    Product
    Self-Cath¿ Pediatric Catheter Size CH 06, Product # 5044101400, Catakig # 306. Product Usage: The Self-Cath intermittent urinary catheter discussed in this document is a pediatric size CH06 French catheter. The catheter is indicated for use by patients with chronic urine ret
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1543-2016·2016-04-27

    Smith & Nephew Recalls TC-Plus Tibial Knee Prosthesis Components

    Smith & Nephew is recalling 6 units of TC-Plus tibial knee prosthesis components due to a dimensional deviation that may prevent proper seating of the polyethylene insert during surgery.

    Product
    TC-PLUS(TM), Primary Fixed Tibial Component VKS Right, SIZE 10 RIGHT, STERILE R, REF 12 000 0013, S&N 7500268, Smith & Nephew Orthopaedics AG Product Usage: Tibial knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1090-2016·2016-04-27

    Brett Anthony Foods Recalls Wild Mushroom Soup for Undeclared Chestnuts

    Brett Anthony Foods is recalling 24 oz containers of Wild Mushroom Soup because the product is mislabeled and does not declare chestnuts.

    Product
    Wild Mushroom Soup packaged in a 24 oz clear plastic container with green and white label and green lettering.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1519-2016·2016-04-27

    Siemens SOMATOM Definition AS CT Systems Recalled for Software Bugs

    Siemens is recalling 1,096 SOMATOM Definition AS CT systems due to software bugs that may cause scan aborts, rescans, or accidental radiation.

    Product
    Siemens SOMATOM Definition AS; Intended to produce cross-sectional images of the body. Computed tomography (CT) x-ray system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1520-2016·2016-04-27

    Siemens SOMATOM Definition Flash CT Systems Recalled for Software Bugs

    Siemens Medical Solutions is recalling 1,096 CT systems due to software bugs that may cause scan aborts, rescans, or accidental radiation.

    Product
    Siemens SOMATOM Definition Flash; Intended to produce cross-sectional images of the body. Computed tomography (CT) x-ray system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1096-2016·2016-04-27

    Chicago Kimchee Recalls Kimchee for Undeclared Anchovies

    Chicago Kimchee is recalling chopped Kimchee products due to undeclared anchovies, a major food allergen.

    Product
    Korea chopped Kimchee packaged in 1 gallon, 1/2 gallon, 1/4 gallon, and 1/8 gallon packaged in glass jars inside plastic containers with multi colored label and black lettering.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1083-2016·2016-04-27

    Hill Country Fare Chunk Light Tuna Recalled for Underprocessing

    HEB is recalling 5,376 cans of Hill Country Fare Chunk Light Tuna in Texas because the product may have been underprocessed.

    Product
    Hill Country Fare Chunk Light Tuna in pure vegetable oil NET WT. 5 OZ (142g) packaged in a metal can.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1009-2016·2016-04-27

    True Nature Garlic Hummus Recalled for Undeclared Soy

    True Nature LLC is recalling Garlic Hummus due to undeclared soy from the ingredient Tamari. The product was sold in Oregon and Washington.

    Product
    Garlic Hummus - 9 oz container
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1086-2016·2016-04-27

    Sara Lee Bread Recalled for Possible Glass Contamination

    BIMBO Bakeries USA Inc. is recalling specific Sara Lee bread products due to possible glass contamination. Consumers should check their bags for the listed dates and UPCs.

    Product
    Sara Lee Delightful 100% Whole Wheat made with Real Honey Bread 20oz On bag: AUG 29 UPC: 7294571589; Sara Lee Honey Wheat Bread; 20 oz; On bag: SEP 01 UPC: 7294560136; Sara Lee Honey Wheat Bread Twin pack 2 lbs 8oz On bag: SEP 01 UPC: 7294561159;
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-1511-2016·2016-04-27

    Ossur Lil Angel Vest Recalled for Potential Plastic Strap Fracture

    Ossur H / F is recalling Lil Angel Vest P2 Lambswool units because the plastic stabilizer strap may partially or completely fracture.

    Product
    Ossur Lil Angel Vest P2 Lambswool. Pediatric sized vest is a support structure used with the halo system for traumatic or chronic disorders requiring traction along the cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1539-2016·2016-04-27

    Smith & Nephew Recalls TC-PLUS Tibial Knee Prosthesis Components

    Smith & Nephew is recalling three TC-PLUS tibial knee prosthesis components due to a dimensional deviation that may prevent proper seating of the polyethylene insert during surgery.

    Product
    TC-PLUS(TM), Primary Fixed Tibial Component VKS Left, SIZE 10 LEFT, STERILE R, REF 12 000 006, S&N 7500261, Smith & Nephew Orthopaedics AG Product Usage: Tibial knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1502-2016·2016-04-27

    Spacelabs Xhibit Telemetry Receiver Recall for Signal Loss

    Spacelabs Healthcare is recalling Xhibit Telemetry Receivers due to frequent signal loss that may cause offline errors on central monitors.

    Product
    The Spacelabs Healthcare Xhibit Telemetry Receiver (XTR), Model 96280 is used to transmit patient(s) physiological measurements and data to a monitor.
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Devices)·Z-1518-2016·2016-04-27

    Siemens SOMATOM Definition CT Systems Recalled for Software Bugs

    Siemens Medical Solutions USA is recalling 1,096 SOMATOM Definition CT systems due to software bugs that may cause scan aborts, re-scans, or accidental radiation.

    Product
    Siemens SOMATOM Definition: Intended to produce cross-sectional images of the body. Computed tomography (CT) x-ray system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1544-2016·2016-04-27

    Smith & Nephew Recalls TC-Plus Tibial Knee Prosthesis Components

    Smith & Nephew is recalling 24 units of TC-Plus tibial knee prosthesis components due to a dimensional deviation that may prevent proper seating during surgery.

    Product
    TC-PLUS(TM), Primary Fixed Tibial Component VKS Left, SIZE 4 LEFT, STERILE R, REF 12 000 017, S&N 7500272, Smith & Nephew Orthopaedics AG Product Usage: Tibial knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1122-2016·2016-04-27

    Servatii Christmas Cookie Tray Recalled for Misleading Allergen Labeling

    Servatii Inc is recalling Christmas Cookie Trays because the labels do not accurately describe allergens, including butter, margarine, and nuts.

    Product
    SERVATii Pastry Shop & Deli 12" Christmas Cookie Tray INGREDIENTS: ***Butter, Margarine***Nuts***1.51lb(682gr) EUROPEAN SPECIALTIES Cincinnati, Ohio 45227 UPC 0 36746 03992 9
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1514-2016·2016-04-27

    Ossur Lil Angel Vest Recalled for Potential Plastic Strap Fracture

    Ossur H / F is recalling Lil Angel Vest P3 Lambswool units because the plastic stabilizer strap may fracture. The recall covers 435 units distributed in the US and Hong Kong.

    Product
    Ossur Lil Angel Vest P3 Lambswool. Pediatric sized vest is a support structure used with the halo system for traumatic or chronic disorders requiring traction along the cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1549-2016·2016-04-27

    Smith & Nephew Recalls TC-Plus Tibial Knee Prosthesis Components

    Smith & Nephew is recalling 34 units of TC-Plus tibial knee prosthesis components due to a dimensional deviation that may prevent proper seating during surgery.

    Product
    TC-PLUS(TM), Primary Fixed Tibial Component VKS Right, SIZE 8 RIGHT, STERILE R, REF 12 000 026, S&N 7500281, Smith & Nephew Orthopaedics AG Product Usage: Tibial knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1538-2016·2016-04-27

    Smith & Nephew Recalls TC-PLUS Tibial Knee Prosthesis Components

    Smith & Nephew is recalling six units of TC-PLUS tibial knee prosthesis components due to a dimensional deviation that may prevent the polyethylene insert from seating correctly during surgery.

    Product
    TC-PLUS(TM), Primary Fixed Tibial Component VKS Left, SIZE 8 LEFT, STERILE R, REF 12 000 005, S&N 7500260, Smith & Nephew Orthopaedics AG Product Usage: Tibial knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1537-2016·2016-04-27

    Smith & Nephew Recalls TC-PLUS Knee Prosthesis Due to Dimensional Deviation

    Smith & Nephew is recalling two units of the TC-PLUS Primary Fixed Tibial Component due to a dimensional deviation that may prevent the polyethylene insert from seating properly during surgery.

    Product
    TC-PLUS(TM), Primary Fixed Tibial Component VKS Left, SIZE 2 LEFT, STERILE R, REF 12 000 002, S&N 7500257, Smith & Nephew Orthopaedics AG Product Usage: Tibial knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1507-2016·2016-04-27

    Stryker Recalls VariAx Compression Plating System Due to Screw Failure

    Stryker Howmedica Osteonics Corp. is recalling 118 units of the VariAx Compression Plating System because bone screws may pass through oblong holes during insertion.

    Product
    VariAx Compression Plating System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1512-2016·2016-04-27

    Ossur Lil Angel Vest Recalled Due to Potential Plastic Strap Fracture

    Ossur H / F is recalling Lil Angel Vest P2 Sorbatex pediatric vests because the plastic stabilizer strap may partially or completely fracture.

    Product
    Ossur Lil Angel Vest P2 Sorbatex. Pediatric sized vest is a support structure used with the halo system for traumatic or chronic disorders requiring traction along the cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1091-2016·2016-04-27

    Aldi Season's Choice Prince Edward Medley Recalled for Listeria

    Camericam International Inc. is recalling Aldi Season's Choice Prince Edward Medley because a limited number of products tested positive for Listeria monocytogenes.

    Product
    Seasons Choice Prince Edward Medley Net Wt. 16 oz. Distributed by: Aldi Inc. Batavia, IL 60510 Product of Netherlands UPC will be entered.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1545-2016·2016-04-27

    Smith & Nephew Recalls TC-Plus Tibial Knee Components Due to Dimensional Deviation

    Smith & Nephew is recalling 22 units of TC-Plus tibial knee components distributed in Germany and Switzerland due to a dimensional deviation that may prevent proper seating of the polyethylene insert.

    Product
    TC-PLUS(TM), Primary Fixed Tibial Component VKS Left, SIZE 6 LEFT, STERILE R, REF 12 000 018, S&N 7500273, Smith & Nephew Orthopaedics AG Product Usage: Tibial knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1505-2016·2016-04-27

    Philips AutoSPECT Pro Software Recalled for Incorrect Cardiac Image Reconstruction

    Philips Medical Systems is recalling the AutoSPECT Pro software application because it may incorrectly reconstruct cardiac SPECT data acquired with non-standard detector angles.

    Product
    Extended Brilliance Workspace NM Special Nuclear medicine image display and processing application suite. AutoSPECT Pro Software Application. Philips Medical Systems, Cleveland, OH. Provides software applications used to process, analyze, and display medical images/data.
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-1542-2016·2016-04-27

    Smith & Nephew Recalls TC-PLUS Knee Prosthesis Due to Dimensional Deviation

    Smith & Nephew is recalling specific TC-PLUS knee prostheses because a dimensional deviation may prevent surgeons from seating the polyethylene insert during surgery.

    Product
    TC-PLUS(TM), Primary Fixed Tibial Component VKS Right, SIZE 8 RIGHT, STERILE R, REF 12 000 0012, S&N 7500267, Smith & Nephew Orthopaedics AG Product Usage: Tibial knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1540-2016·2016-04-27

    Smith & Nephew Recalls TC-Plus Knee Prosthesis Due to Dimensional Deviation

    Smith & Nephew is recalling one unit of a TC-Plus knee prosthesis due to a dimensional deviation that may prevent the polyethylene insert from seating correctly during surgery.

    Product
    TC-PLUS(TM), Primary Fixed Tibial Component VKS Right, SIZE 2 RIGHT, STERILE R, REF 12 000 009, S&N 7500264, Smith & Nephew Orthopaedics AG Product Usage: Tibial knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1548-2016·2016-04-27

    Smith & Nephew Recalls TC-PLUS Knee Prosthesis Components

    Smith & Nephew is recalling 33 units of TC-PLUS tibial knee prosthesis components due to a dimensional deviation that may prevent proper assembly during surgery.

    Product
    TC-PLUS(TM), Primary Fixed Tibial Component VKS Right, SIZE 6 RIGHT, STERILE R, REF 12 000 025, S&N 7500280, Smith & Nephew Orthopaedics AG Product Usage: Tibial knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1499-2016·2016-04-27

    Leica Surgical Microscopes Recalled for Potential Overheating and Smoke

    Leica Microsystems is recalling 381 M525 and M720 surgical microscopes because an electronic component may overheat, causing smoke and smell.

    Product
    Leica Microsystems (Schweiz) Ag. The common name of the device is surgical microscope. It has been assigned the product code FSO by the FDA and is classified as a Class I medical device. Intended for improving the visibility of objects through magnification and illumination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1541-2016·2016-04-27

    Smith & Nephew Recalls TC-Plus Tibial Knee Prosthesis Components

    Smith & Nephew is recalling four units of TC-Plus tibial knee prosthesis components due to a dimensional deviation that may prevent proper seating during surgery.

    Product
    TC-PLUS(TM), Primary Fixed Tibial Component VKS Right, SIZE 6 RIGHT, STERILE R, REF 12 000 0011, S&N 7500266, Smith & Nephew Orthopaedics AG Product Usage: Tibial knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1510-2016·2016-04-27

    Ossur Lil Angel Vest P2 Kodel Recalled for Potential Plastic Strap Fracture

    Ossur H / F is recalling 435 Lil Angel Vest P2 Kodel units due to a potential for partial or complete fracture of the plastic stabilizer strap.

    Product
    Ossur Lil Angel Vest P2 Kodel. Pediatric sized vest is a support structure used with the halo system for traumatic or chronic disorders requiring traction along the cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1081-2016·2016-04-27

    Starbucks Cheese and Fruit Bistro Box Recalled for Undeclared Cashews

    Flying Foods LLC is recalling Starbucks Cheese & Fruit Bistro Boxes because they may contain undeclared cashews. The product was distributed in Florida, Texas, and Oklahoma.

    Product
    Starbuck's Cheese & Fruit Bistro Box NET WT 5.3 OZ/150g packaged in non-flexible plastic container.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1546-2016·2016-04-27

    Smith & Nephew Recalls TC-PLUS Knee Prosthesis Due to Dimensional Deviation

    Smith & Nephew is recalling 15 units of TC-PLUS Primary Fixed Tibial Components due to a dimensional deviation that may prevent proper seating of the polyethylene insert.

    Product
    TC-PLUS(TM), Primary Fixed Tibial Component VKS Left, SIZE 8 LEFT, STERILE R, REF 12 000 019, S&N 7500274, Smith & Nephew Orthopaedics AG Product Usage: Tibial knee prosthesis
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0831-2016·2016-04-27

    Hospira Recalls Mannitol I.V. Bags Due to Chemical Contamination Risk

    Hospira Inc. is recalling 22,292 bags of Mannitol I.V. 20% due to potential contamination with an aromatic hydrocarbon resin.

    Product
    Mannitol I.V., 20%, USP (20 g/ 100 mL), Packaged in 250 mL Bags, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC: 0409-7715-02, Barcode (01) 0 030409 771502 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1500-2016·2016-04-27

    Siemens ADVIA 560 Hematology System Software Recall

    Siemens is recalling ADVIA 560 Hematology Systems because a software defect prevents the system from flagging immature granulocytes and atypical lymphocytes in patient samples.

    Product
    ADVIA 560 Hematology Systems, Siemens Material Number (SMN) 11170842, IVD The ADVIA 560 Hematology System is a fully-automated, high-quality hematology system for in vitro diagnostic use in clinical laboratories
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-1342-2016·2016-04-27

    Boston Scientific Recalls Fetch 2 Aspiration Catheters Due to Shaft Breaks

    Boston Scientific is recalling Fetch 2 Aspiration Catheters because the catheter shafts may break, potentially requiring additional procedures to remove the broken piece from patients.

    Product
    Boston Scientific Fetch 2 Aspiration Catheter, Catalog No. 109400-001. Product The Fetch 2 Aspiration Catheter is indicated for the removal of fresh, soft emboli and thrombi from vessels in the peripheral and coronary vasculature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1506-2016·2016-04-27

    Philips AutoSPECT Pro Software Recalled for Incorrect Cardiac Image Reconstruction

    Philips Medical Systems is recalling 33 units of AutoSPECT Pro software because it may incorrectly reconstruct cardiac SPECT data acquired at non-standard detector angles.

    Product
    IntelliSpace Portal DX/HX/EX AutoSPECT Pro Software Application, Philips Medical Systems, Cleveland, OH. Provides software applications used to process, analyze, and display medical images/data.
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-1513-2016·2016-04-27

    Ossur Lil Angel Vest Recalled for Potential Plastic Strap Fracture

    Ossur H / F is recalling Lil Angel Vest P3 Kodel units due to a potential for partial or complete fracture of the plastic stabilizer strap.

    Product
    Ossur Lil Angel Vest P3 Kodel. Pediatric sized vest is a support structure used with the halo system for traumatic or chronic disorders requiring traction along the cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1515-2016·2016-04-27

    Ossur Lil Angel Vest Recalled for Potential Plastic Strap Fracture

    Ossur H / F is recalling Lil Angel Vest P3 Sorbatex units because the plastic stabilizer strap may partially or completely fracture.

    Product
    Ossur Lil Angel Vest P3 Sorbatex. Pediatric sized vest is a support structure used with the halo system for traumatic or chronic disorders requiring traction along the cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1114-2016·2016-04-27

    Materne Recalls GoGo squeeZ Applesauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ applesauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, Apple/Pumpkin Spice Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1105-2016·2016-04-27

    Materne Recalls GoGo squeeZ Applesauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ applesauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12 x4, Apple/Pear Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1093-2016·2016-04-27

    Gerber Recalls Organic Infant Pouches Due to Packaging Air Holes

    Gerber is voluntarily recalling two batches of Organic 2ND FOODS pouches because packaging defects may allow air in, leading to mold, yeast, and spoilage.

    Product
    GERBER Organic 2ND FOODS Pears, Carrots & Peas, 3.5 oz., film pouches, 6 pouches per display box/ 2 display boxes per case; Asst Ecom PK2 18 pc, 3.94 Lbs.
    Category
    Food
    Distribution
    36 states
  • ModerateFDA (Food)·F-1109-2016·2016-04-27

    Materne Recalls GoGo squeeZ Applesauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ applesauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 4x18, Apple/Berry Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1117-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, Apple/Mixed Berry/Carrot (Boulder Berry) Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1104-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches for Potential Adulteration

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12 x4, 6 x12, 1 x 18, 1 x 48, 1 x100, 36 x 4, Mighty Mango Fruit & Veggies on the Go, (Apple/Mango/ButternutSquash) Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0827-2016·2016-04-27

    Hospira Recalls Dextrose Injection Bags Due to Chemical Contamination Risk

    Hospira is recalling 11,256 bags of Dextrose Injection, USP, 70% due to potential contamination with an aromatic hydrocarbon resin.

    Product
    Dextrose Injection, USP, 70%, Packaged as 500 mL in 1000 mL Bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7918-19, Barcode (01) 0 030409 791819 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1113-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    Gogo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, Apple/Strawberry Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1094-2016·2016-04-27

    Gerber Organic 2nd Foods Pouches Recalled for Packaging Air Holes

    Nestle Infant Nutrition is voluntarily recalling two batches of Gerber Organic 2nd Foods pouches because packaging air holes may cause mold and yeast growth.

    Product
    GERBER Organic 2ND FOODS¿ Carrots, Apples & Mangoes, 3.5 oz., film pouches, 6 pouches per display box/ 2 display boxes per case, 9Pc AsstA CbPk 1.96 Lbs; Asst EcomPk1 18 pc, 3.94 Lbs.; 48 Pc 10.48 Lbs.; 4 x 3.5 oz.
    Category
    Food
    Distribution
    36 states
  • ModerateFDA (Food)·F-1107-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12 x4, 6 x12, 1x18, 4 x16, Apple/Cinnamon Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateNHTSA·16T006000·2016-04-27

    Pirelli Recalls Tires Missing Required Date Codes

    Pirelli is recalling specific P Zero Trofeo tires that may lack required date codes, which could hinder identification during safety issues.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1095-2016·2016-04-27

    Centro Naturista Recalls Smart Lipo Dietary Supplement Capsules

    Centro Naturista is recalling Smart Lipo dietary supplements due to multiple regulatory violations. Consumers should stop using the product.

    Product
    Smart Lipo Dietary Supplement capsules, 950 mg, packaged in 30-count plastic bottle, Distributed by: SmartLipo365, Arlington, TX 76011
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1116-2016·2016-04-27

    Materne Recalls GoGo squeeZ Applesauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ applesauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, Apple/Peach/SweetPotato (Pedal Pedal Peach) Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1115-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches Due to Residue

    Materne North America Corp is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, Apple/Pear/Carrot (Zippin'Zingin'Pear) Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1111-2016·2016-04-27

    Materne Recalls GoGo squeeZ Apple Sauce Pouches Due to Residue

    Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.

    Product
    GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12x4, 6 x 12, Apple/Mango Flavor Variety
    Category
    Food
    Distribution
    Distributed nationwide

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