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.

401–500 of 764

  • LowFDA (Food)·F-0829-2016·2016-04-20

    Pioneer Brand Buttermilk Pancake Mix Recalled for Metal Fragments

    Morrison Milling is recalling Pioneer Brand Original Buttermilk Pancake and Waffle Mix because it may contain small metal fragments from a wire mesh sifter.

    Product
    Pioneer Brand Original Buttermilk Pancake and Waffle Mix Premium Quality NET WT 32 oz. (2 lb) 907g packed in paper box
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0852-2016·2016-04-20

    Morrison Milling Recalls FBR Batter Mix for Metal Fragments

    Morrison Milling is recalling FBR Batter Mix because it may contain small metal fragments from a wire mesh sifter.

    Product
    FBR Batter Mix NET WT 30 LBS (13.61 kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0854-2016·2016-04-20

    Morrison Milling Recalls Tempura Batter Mix Due to Metal Fragments

    Morrison Milling is recalling Original Tempura Batter Mix because it may contain small metal fragments from a wire mesh sifter.

    Product
    Original Tempura Batter Mix Net Weight 5 Lbs (2.27 KG)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0889-2016·2016-04-20

    Morrison's Pancake Mix Recalled for Potential Metal Fragments

    Morrison's Pancake Mix is being recalled because it may contain small metal fragments from a wire mesh sifter.

    Product
    Morrison's Pancake Mix Net Wt 5 LB (2.27 kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0817-2016·2016-04-20

    Biocon Recalls Subpotent Simvastatin Tablets Due to Quality Concerns

    Biocon Inc is voluntarily recalling 5,505 bottles of Simvastatin Tablets USP 5 mg because the drug was found to be subpotent. The affected lots were distributed in Pennsylvania, California, and Ohio.

    Product
    Simvastatin Tablets, USP 5 mg Rx only, a) 90 count (NDC 24658-0300-90) and b) 1000 count (NDC 24658-0300-10 )bottles, Manufactured by: Blu Caribe Dorado PR 00646, Manufactured for: Blu Pharmaceuticals Franklin, KY 42134
    Category
    Drug
    Distribution
    3 states
  • LowFDA (Food)·F-0899-2016·2016-04-20

    Pioneer Buttermilk Pancake Mix Recalled for Metal Fragment Risk

    Morrison Milling is recalling Pioneer Buttermilk Pancake Mix because it may contain small metal fragments from a wire mesh sifter.

    Product
    Pioneer Buttermilk Pancake Mix NET WT 5 LBS (2.27 kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0886-2016·2016-04-20

    Ben E. Keith Pancake Mix Recalled for Potential Metal Fragments

    Ben E. Keith Keith's Exclusive Complete Pancake Mix is being recalled because it may contain small metal fragments from a wire mesh sifter.

    Product
    Ben E. Keith Keith's Exclusive Complete Pancake Mix NET WT 5 lb (2.27 kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0869-2016·2016-04-20

    Morrison's Cornbread Mix Recalled for Potential Metal Fragments

    Morrison's Home Style Cornbread Mix is being recalled because it may contain small metal fragments from a wire mesh sifter.

    Product
    Morrison's Home Style Cornbread Mix NET WT 5 LB (2.27 kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0821-2016·2016-04-20

    Impax Recalls Fenofibrate Capsules Due to Incorrect or Missing Labeling

    Impax Laboratories is recalling 42,239 bottles of Fenofibrate Capsules (Micronized) 200 mg because some bottles have incorrect or missing lot and expiration dates.

    Product
    Fenofibrate Capsules (Micronized) 200 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0533-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0830-2016·2016-04-20

    Pioneer Brand Buttermilk Pancake Mix Recalled for Metal Fragments

    Morrison Milling is recalling Pioneer Brand No Fat Complete Buttermilk Pancake & Waffle Mix because it may contain small metal fragments from a wire mesh sifter.

    Product
    Pioneer Brand No Fat Complete Buttermilk Pancake & Waffle Mix Premium Quality NET WT 32 oz. (2 lb) 907g packed in paper box
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0879-2016·2016-04-20

    Pioneer Multi-Grain Pancake Mix Recalled for Metal Fragments

    Morrison Milling is recalling Pioneer Multi-Grain Pancake & Waffle Mix because it may contain small metal fragments from a wire mesh sifter.

    Product
    Pioneer Mulit-Grain Pancake & Waffle Mix NET WT 5 LBS (2.27 kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0832-2016·2016-04-20

    Morrison Milling Recalls HEB Cornbread Mix for Metal Fragment Risk

    Morrison Milling is recalling HEB Rosemary Olive Oil with Sea Salt Cornbread Mix because it may contain small metal fragments from a wire mesh sifter.

    Product
    HEB Rosemary Olive Oil with Sea Salt Cornbread Mix NET WT. 13.3 OZ (377g) packed in paper box
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0878-2016·2016-04-20

    Conestoga Buttermilk Pancake Mix Recalled for Metal Fragment Risk

    Morrison Milling is recalling Conestoga Buttermilk Pancake & Waffle Mix because it may contain small metal fragments from a wire mesh sifter.

    Product
    Conestoga Buttermilk Pancake & Waffle Mix NET WT 25 LB (11.34 kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1390-2016·2016-04-20

    BD Retic-Count Reagent System Recalled for Incorrect Storage Labeling

    Becton, Dickinson and Company is recalling one lot of BD Retic-Count Reticulocyte Reagent System because the carton label listed incorrect storage conditions.

    Product
    BD-Retic-Count Reticulocyte Reagent System; Hematology: Used for in vitro diagnostics
    Category
    Medical Device
    Distribution
    10 states
  • LowFDA (Food)·F-0831-2016·2016-04-20

    Pioneer Brand Maple Flavor Pancake Mix Recalled for Metal Fragments

    C. H. Guenther & Son is recalling Pioneer Brand Maple Flavor Pancake Mix because it may contain small metal fragments from a wire mesh sifter.

    Product
    Pioneer Brand Maple Flavor Pancake & Waffle Complete Mix Premium Quality NET WT 6 oz. (170g) packed in paper box
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0900-2016·2016-04-20

    Morrison's Cornmeal Mix Recalled for Potential Metal Fragments

    Morrison's Self-Rising Cornmeal Mix is being recalled because it may contain small metal fragments from a wire mesh sifter.

    Product
    Morrison's Premuim Self-Rising Cornmeal Mix NET WT 25 LB (11.33 kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0875-2016·2016-04-20

    Morrison Milling Recalls Legendary Baking Trans Fat Free Flour

    Morrison Milling is recalling 1,911 cases of Legendary Baking Trans Fat Free flour nationwide due to potential small metal fragments from a wire mesh sifter.

    Product
    Legendary Baking Trans Fat Free 93375
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0847-2016·2016-04-20

    Pioneer Hush Puppy Mix Recalled for Potential Metal Fragments

    Morrison Milling is recalling Pioneer Hush Puppy Mix because it may contain small metal fragments from a wire mesh sifter.

    Product
    Pioneer Hush Puppy Mix NET WT 5 LB 2.27 kg
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0837-2016·2016-04-20

    Parade Cornbread Mix Recalled for Potential Metal Fragments

    Morrison Milling is recalling Parade Cornbread Mix White due to the potential presence of small metal fragments from a wire mesh sifter.

    Product
    Parade Cornbread Mix White NET WT/PESO NETO 6 OZ (170g) packed in paper box
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0823-2016·2016-04-20

    Amerisource Recalls Fenofibrate Capsules Due to Incorrect or Missing Labeling

    Amerisource Health Services is recalling 5,034 cartons of Fenofibrate Capsules (Micronized), 200 mg, due to incorrect or missing lot and expiration dates.

    Product
    Fenofibrate Capsules (Micronized), 200 mg , 30-count Unit Dose Blister Packs per carton, Rx Only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217 Carton of 30:NDC 68084-835-32, Individual Dose: NDC 68084-835-33.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0820-2016·2016-04-20

    Impax Recalls Fenofibrate Capsules Due to Incorrect or Missing Labeling

    Impax Laboratories is recalling 28,001 bottles of Fenofibrate Capsules (Micronized) 134 mg because the bottles have incorrect or missing lot and expiration dates.

    Product
    Fenofibrate Capsules (Micronized) 134 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0522-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0895-2016·2016-04-20

    Razzoo's Seasoned Corn Flour Recalled for Potential Metal Fragments

    Morrison Milling is recalling Razzoo's Seasoned Corn Flour because it may contain small metal fragments from a wire mesh sifter.

    Product
    Razzoo's Seasoned Corn Flour NET WT 25 LB (11.33 kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0822-2016·2016-04-20

    Amerisource Health Services Recalls Fenofibrate Capsules Due to Labeling Errors

    Amerisource Health Services is recalling 228 cartons of Fenofibrate Capsules because some units have incorrect or missing lot and expiration dates.

    Product
    Fenofibrate Capsules (Micronized), 134 mg Capsules, 20-count Unit Dose Blister Packs per carton, Rx Only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217, Carton of 20: NDC 68084-835-32, Individual Dose: NDC 68084-835-33.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0834-2016·2016-04-20

    Morrison Milling Recalls HEB Cheddar Bacon Cornbread Mix for Metal Fragments

    Morrison Milling is recalling HEB Cheddar Bacon Flavored Cornbread Mix because it may contain small metal fragments from a wire mesh sifter.

    Product
    HEB Cheddar Bacon Flavored Cornbread Mix NET WT. 13.3 OZ (377g) packed in paper box
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0872-2016·2016-04-20

    Ben E. Keith Cornbread Mix Recalled for Metal Fragments

    Morrison Milling is recalling Ben E. Keith Home Style Cornbread Mix because it may contain small metal fragments from a wire mesh sifter.

    Product
    Ben E. Keith Home Style Cornbread Mix NET WT 5 lb. (2.27kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0818-2016·2016-04-20

    Fresenius Kabi Recalls Haloperidol Decanoate Injection Due to Impurity

    Fresenius Kabi USA, LLC is recalling Haloperidol Decanoate Injection due to an impurity out-of-specification result. The recall affects 48,210 units distributed nationwide and in Puerto Rico.

    Product
    HALOPERIDOL DECANOATE — HALOPERIDOL DECANOATE (HALOPERIDOL DECANOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1350-2016·2016-04-20

    Siemens Recalls One CT System Due to Front Cover Welding Defect

    Siemens is recalling one SOMATOM Definition AS CT system because a front cover weld defect could cause a bolt to break during service, though no clinical risk exists.

    Product
    SOMATOM Definition AS, a family of CT systems intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission dta from either the same axial plane taken at different angles or spiral planes taken at different angles.
    Category
    Medical Device
    Distribution
    0 states
  • CriticalCPSC·16146·2016-04-19

    Polaris Recalls RZR Recreational Off-Highway Vehicles Due to Fire Hazard

    Polaris is recalling about 133,000 RZR recreational off-highway vehicles because they can catch fire while driving, posing fire and burn hazards.

    Product
    Polaris RZR recreational off-highway vehicles (ROVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V225000·2016-04-19

    Forest River Recalls 2016 Glaval Buses Due to Seat Separation Risk

    Forest River is recalling 2016 Glaval Entourage and Universal buses because seats may separate from the base frame due to bolt failure, increasing injury risk in a crash.

    Product
    GLAVAL BUS — GLAVAL BUS ENTOURAGE, UNIVERSAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16148·2016-04-19

    Brunton Recalls Rechargeable Battery Packs Due to Fire Hazard

    Brunton Outdoor Inc. is recalling Impel and Impel 2 rechargeable battery packs because they can overheat and catch fire during charging.

    Product
    Rechargeable battery packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16147·2016-04-19

    Flying Tiger Copenhagen Recalls Wooden Toys Due to Choking Hazard

    Flying Tiger Copenhagen is recalling wooden blocks and giraffe toys because parts can detach and pose a choking hazard to young children.

    Product
    Wooden Toy Blocks and Giraffes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V223000·2016-04-19

    New Flyer Transit Buses Recalled for Rear Door Software Defect

    New Flyer is recalling specific transit buses because a software defect may cause the rear door to open unexpectedly while the bus is moving, increasing injury risk.

    Product
    NEW FLYER — NEW FLYER XN40, XN60, C40LFR, XN35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·030-2016·2016-04-16

    AdvancePierre Recalls Breaded Pork Patties for Undeclared Egg Allergen

    AdvancePierre Foods is recalling approximately 3,469 pounds of breaded pork patties because they contain eggs, a known allergen, that are not declared on the label.

    Product
    AdvancePierre Foods, Inc. — Advancepierre Foods Recalls Pork Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    4 states
  • HighCPSC·16145·2016-04-15

    Miniland Recalls Moogy Plush Toys Due to Choking Hazard

    Miniland Educational is recalling Moogy plush toys because buttons can detach, posing a choking hazard to young children.

    Product
    Moogy plush toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V215000·2016-04-14

    Toyota Recalls 2016 Camry and Avalon for Air Bag Calibration Issues

    Toyota is recalling 58,515 model year 2016 Camry and Avalon vehicles because the occupant classification system may be improperly calibrated, potentially preventing front passenger air bags from deploying.

    Product
    TOYOTA — TOYOTA CAMRY, AVALON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V217000·2016-04-14

    Glaval Bus Transit Models Recalled for Emergency Exit Label Placement

    Forest River is recalling 2008-2016 Glaval Bus transit models because rear emergency exit labels are not placed within 16 centimeters of release mechanisms, potentially hindering quick escape.

    Product
    GLAVAL BUS — GLAVAL BUS TITAN II, APOLLO, TITAN II LOW FLOOR, TITAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E035000·2016-04-14

    Steve Johnson Induction Solutions Recalls Nitrous Oxide Solenoid Valves

    Steve Johnson Induction Solutions is recalling specific nitrous oxide solenoid valves because end stops may break under pressure, posing an injury risk.

    Product
    FUEL SYSTEM, OTHER:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16143·2016-04-14

    Fisher-Price Recalls Infant Cradle Swings Due to Fall Hazard

    Fisher-Price is recalling about 34,000 infant cradle swings because the seat peg may not be fully engaged, allowing the seat to fall unexpectedly.

    Product
    Cradle 'n Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1275-2016·2016-04-13

    FDA Recalls Guardian II Hemostasis Valves Due to Air Embolism Risk

    Vascular Solutions is recalling Guardian II Hemostasis Valves because the low-pressure seal may fail, potentially allowing air into the device and causing an air embolism.

    Product
    Guardian II Hemostasis Valve, models 8210 and 8211. The following models are only available Outside the US: FH101, FH101-T, FH101-25, and FH101-50. Product Usage: The Guardian hemostasis valves are designed to be used as conduits when interventional devices with diameters
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1030-2016·2016-04-13

    Country Life Raw Pistachios Recalled for Potential Salmonella Contamination

    Country Life Natural Foods is recalling raw shelled pistachios due to potential Salmonella contamination. The product was sold in 2 lb bags and 30 lb boxes.

    Product
    SAM International RAW WHOLE PISTACHIO 80%VP Labeled 30 pound box
    Category
    Food
    Distribution
    14 states
  • CriticalFDA (Food)·F-1027-2016·2016-04-13

    R.J. Van Drunen Recalls Organic Spinach Powder Due to Salmonella

    R.J. Van Drunen & Sons is recalling 4,398.59 pounds of air-dried organic spinach powder because an FDA sample tested positive for Salmonella.

    Product
    Air dried Organic Spinach Powder packaged in 50 lb. polyethylene liner inside of a cardboard box.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0904-2016·2016-04-13

    Peking Food LLC Recalls Chef Hon Steamed Buns for Undeclared Eggs

    Peking Food LLC is recalling Chef Hon brand steamed buns with seafood because they contain undeclared eggs. The product was distributed across 22 states and Puerto Rico.

    Product
    Chef Hon brand STEAMED BUNS WITH SEAFOOD MARINATED IN XO-SAUCE, Net Wt. 1 lb. 8 oz. (682g), UPC 7 47518 00163 0, KEEP FROZEN --- Peking Food LLC Brooklyn, NY
    Category
    Food
    Distribution
    22 states
  • CriticalFDA (Food)·F-1028-2016·2016-04-13

    GSN Organic Mediterranean Blend Recalled for Salmonella Contamination

    R.J. Van Drunen & Sons is recalling GSN organic Mediterranean Blend because an FDA sample tested positive for Salmonella.

    Product
    GSN organic Mediterranean Blend packaged in 44 lb. polyethylene liner inside of a cardboard box.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1020-2016·2016-04-13

    Country Life Raw Shelled Pistachios Recalled for Salmonella Risk

    Country Life Natural Foods is recalling raw shelled pistachios due to potential Salmonella contamination.

    Product
    Country Life Natural Foods Labeled SHELLED PISTACHIOS RAW NET WT. 2lb (906 g) plastic bags item 030244 and Batch 1357 batch number 1357 in the lower left corner of the label
    Category
    Food
    Distribution
    14 states
  • CriticalFDA (Food)·F-1019-2016·2016-04-13

    Wholesome Soy Mung Bean Sprouts Recalled for Listeria Contamination

    Wholesome Soy Products is recalling mung bean sprouts in Illinois due to Listeria monocytogenes contamination found by FDA environmental sampling.

    Product
    Mung bean sprouts are packaged 1 lb., 5 lbs., 10 lbs., 15 lbs., or 30 lbs. per plastic bag.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1033-2016·2016-04-13

    Sweetwater Sprouts Recalled for Potential Salmonella Contamination

    Sweetwater Farms LLC is recalling sprouted mung beans due to potential Salmonella contamination. The product was distributed in Arkansas, Kansas, and Oklahoma.

    Product
    Sweetwater Sprouts 100% Pure Sprouted Mung Bean packaged in the following configurations: 8 oz. plastic bags packed 10 per case; 16 oz. plastic bags packed in cases of 5 or 10; 5 lb. bulk case; 10 lb. bulk case. The product is shipped in cardboard cases labeled with prod
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-1036-2016·2016-04-13

    Dutch Farmstead Smoked Plain Gouda Recalled for Salmonella

    Dutch Cheesemaking is recalling 3.5-pound packages of Dutch Farmstead Cheese Smoked Plain Gouda because the product tested positive for Salmonella.

    Product
    DUTCH FARMSTEAD CHEESE SMOKED PLAIN GOUDA
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0903-2016·2016-04-13

    Peking Food LLC Recalls Chef Hon Steamed Buns for Undeclared Eggs

    Peking Food LLC is recalling Chef Hon brand steamed buns with seafood and vegetable due to undeclared eggs. The product was distributed across 22 states and Puerto Rico.

    Product
    Chef Hon brand STEAMED BUNS WITH SEAFOOD & VEGETABLE, Net Wt. 1 lb. 8 oz. (682g), UPC 7 47518 00156 2, Product Code # 69, KEEP FROZEN --- Peking Food LLC Brooklyn, NY
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Devices)·Z-1323-2016·2016-04-13

    MicroAire French Rasp Aspiration Cannula Recalled for Bending or Breaking

    MicroAire Surgical Instruments is recalling 37 units of the PAL-R4011XL French Rasp aspiration cannula because they bent or broke during surgery.

    Product
    MicroAire PAL-R4011XL - 40cm x 4 mm Del Vecchio French Rasp aspiration cannula
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V211000·2016-04-13

    Mercedes-Benz Recalls 2016 SLK300 Vehicles Due to Ignition Wiring Defect

    Mercedes-Benz is recalling 2016 SLK300 vehicles because a backup power supply for the ignition switch may not be properly connected, creating a risk of the vehicle rolling.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SLK300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V214000·2016-04-13

    Hillsboro Aluminum Utility Trailer Recall for Axle Hardware Defect

    Hillsboro is recalling 2016 aluminum utility trailers because improperly installed axle hardware may cause the axle to shift, increasing crash risk.

    Product
    HILLSBORO — HILLSBORO ALUMINUM UTILITY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0808-2016·2016-04-13

    Meditech Formula 2 Vials Recalled Due to Expired Active Ingredient

    Meditech Laboratories is recalling Formula 2 vials because an active ingredient expired before the labeled Beyond Use Date.

    Product
    Formula 2 (Papaverine 9 mg, Phentolamine 1 mg, Atropine 0.1 mg, PGE 10 mcg/mL), 5 mL vials, Meditech Laboratories, Inc., 3200 Polaris Ave., Suite 27, Las Vegas, NV 89102.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V213000·2016-04-13

    Karavan Recalls 2016 KPSD Trailers Due to Axle Spindle Flange Defect

    Karavan is recalling 2016 KPSD trailers because a defective axle spindle flange may bend, causing excessive tire wear and increasing the risk of tire failure and a crash.

    Product
    KARAVAN — KARAVAN KPSD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0804-2016·2016-04-13

    Meditech Formula 9 Injection Recalled for Sterility Assurance Issues

    Meditech Laboratories is recalling Formula 9 Injection vials due to incomplete production data regarding sterility assurance.

    Product
    Formula 9 (Papaverine 0.9 mg, Phentolamine 0.1 mg, Atropine 0.01 mg, PGE 20 mcg/mL) Injection, 5 mL vial, Rx only, Meditech Laboratories, Inc., 3200 Polaris Ave., Suite 27, Las Vegas, NV 89102.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0802-2016·2016-04-13

    Meditech Formula 2 Injection Recalled for Superpotent Drug Ingredient

    Meditech Laboratories is recalling Formula 2 Injection vials because one ingredient exceeded assay specifications, making the drug superpotent.

    Product
    Formula 2 (Papaverine 9 mg, Phentolamine 1 mg, Atropine 0.1 mg, PGE 10 mcg/mL) Injection, 5 mL vials, Rx only, Meditech Laboratories, Inc., 3200 Polaris Ave., Suite 27, Las Vegas, NV 89102.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1012-2016·2016-04-13

    Loki Fish Company Recalls Wild Smoked Pink Salmon for Listeria

    Loki Fish Company is recalling Wild Smoked Pink Salmon portions due to a positive test result for Listeria monocytogenes. The product was distributed in Oregon and Washington and sold via mail order to Florida, Georgia, and Ohio.

    Product
    Wild Smoked Pink Salmon, 4-7 ounce portions in clear plastic package. No UPC. Label is read in parts: "***Smoked PINK SALMON***KEEP REFRIGERATED BELOW 38F***LOKI FISH CO***SEATTLE-WA***".
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1032-2016·2016-04-13

    Sweetwater Sprouted Clover Recalled for Potential Salmonella Contamination

    Sweetwater Farms LLC is recalling specific lots of 100% Pure Sprouted Clover due to potential Salmonella contamination. The product was distributed in Arkansas, Kansas, and Oklahoma.

    Product
    Sweetwater Sprouts100% Pure Sprouted Clover packaged in plastic bags and shipped in cardboard cases labeled with product, Net Wt. 5 lb. and lot number. The responsible name on the label is Sweetwater Farms, Inman, KS 67546.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0803-2016·2016-04-13

    Meditech Formula 4 Injection Recalled for Sterility Assurance Issues

    Meditech Laboratories is recalling Formula 4 Injection vials due to incomplete data regarding production sterility.

    Product
    Formula 4 (Papaverine 18 mg, Phentolamine 2 mg, Atropine 0.2 mg/mL) Injection, 5 mL vials, Rx only, Meditech Laboratories, Inc., 3200 Polaris Ave., Suite 27, Las Vegas, NV 89102. .
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0807-2016·2016-04-13

    Meditech Formula 0 Injection Recalled for Sterility Assurance Issues

    Meditech Laboratories is recalling Formula 0 Injection due to incomplete production data regarding sterility assurance.

    Product
    Formula 0 (PGE 20 mcg/mL) Injection, 5 mL vials, Rx only, Meditech Laboratories, Inc., 3200 Polaris Ave., Suite 27, Las Vegas, NV 89102.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0926-2016·2016-04-13

    BJ's Wholesale Club Recalls Cittero Mortadella Due to Undeclared Pistachios

    BJ's Wholesale Club is recalling Cittero Mortadella because it contains undeclared pistachios. The product was sold at 71 locations in eight states.

    Product
    Cittero Mortadella, packaged in deli bags. This is a deli service item.
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-1002-2016·2016-04-13

    Whole Foods Market Recalls Maytag Blue Cheese for Listeria Risk

    Whole Foods Market is recalling Maytag Blue Cheese products due to possible contamination with Listeria monocytogenes.

    Product
    Whole Foods Market Maytag Blue Cheese, Maytag Blue Raw Milk, Maytag Iowa Blue Cheese cut and wrapped in clear plastic wrap, Dist. by Whole Foods Market 550 Bowie Street Austin, TX 78703, PLU: 0293308
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1037-2016·2016-04-13

    NutraKey Recalls VPro Raw Plant Protein Due to Undeclared Soy

    NutraKey, Inc. is recalling VPro Raw Plant Protein, Mocaccino, because it contains undeclared soy. The product was distributed nationwide.

    Product
    VPro Raw Plant Protein, Mocaccino. Packaged in a plastic bottle with green, white, and black adhesive label. Packaged in 1 lb (15 serving) and 2 lb (30 serving).
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0816-2016·2016-04-13

    Actavis Recalls Amphetamine Tablets Due to Impurity Failures

    Actavis is recalling specific lots of amphetamine tablets because they failed impurity specifications. Consumers should stop using the product and contact their pharmacist.

    Product
    Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 5 mg, 100 ct. bottle, Rx Only. Manufactured by: Actavis Elizabeth LLC, Elmora Avenue, Elizabeth, NJ 07207. Distributed by: Actavis, Inc., 80 Columbia Road, Bldg B, Mo
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1327-2016·2016-04-13

    Synthes Recalls Titanium Low Profile Neuro Screws Due to Thread Defect

    Synthes (USA) Products LLC is recalling specific lots of Titanium Low Profile Neuro Screws because the thread height is undersized, potentially compromising the device's structural integrity.

    Product
    Titanium Low Profile Neuro Screw, Self Drilling, 3mm, part numbers: 400.833, 400.833E Product Usage: The Low Profile Neuro Plating System is intended for use in selective trauma of the midface and craniofacial skeleton; craniofacial surgery; reconstructive procedures; and sel
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1315-2016·2016-04-13

    ScottCare TeleSentry Battery Recall Due to Explosion Risk During Recharging

    ScottCare is recalling 9,067 TeleSentry batteries after a complaint that one exploded while recharging. The batteries are used in cardiac monitoring devices.

    Product
    TeleSentry Battery, 3.7 Li-Ion Polymer Battery, CAUTION Do not expose to high temperature. Do not disassemble. Dispose of properly. Use specified charger only. 60pC/140pF The ScottCare Corporation. Intended for diagnostic evaluation of patients who experience transient sympto
    Category
    Medical Device
    Distribution
    24 states
  • SevereFDA (Drugs)·D-0814-2016·2016-04-13

    Actavis Recalls Dextroamphetamine Tablets Due to Impurity Failures

    Actavis Elizabeth LLC is recalling 257,746 bottles of Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 20 mg, because they failed impurity specifications.

    Product
    Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 20 mg, 100 ct. bottle, Rx Only. Manufactured by: Actavis Elizabeth LLC, Elmora Avenue, Elizabeth, NJ 07207. Distributed by: Actavis, Inc., 80 Columbia Road, Bldg B, M
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1038-2016·2016-04-13

    NutraKey Recalls VPro Raw Plant Protein for Undeclared Soy

    NutraKey, Inc. is voluntarily recalling VPro Raw Plant Protein nationwide due to undeclared soy, a major food allergen.

    Product
    VPro Raw Plant Protein, Natural. Packaged in a plastic bottle with green, white, and black adhesive label. Packaged in 2 lb (30 serving).
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1040-2016·2016-04-13

    NutraKey Recalls VPro Raw Plant Protein for Undeclared Soy

    NutraKey, Inc. is voluntarily recalling VPro Raw Plant Protein, Vanilla, due to undeclared soy. The product was distributed nationwide.

    Product
    VPro Raw Plant Protein, Vanilla. Packaged in a plastic bottle with green, white, and black adhesive label. Packaged in 1 lb (15 serving) and 2 lb (30 serving).
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1018-2016·2016-04-13

    Jensens Recalls Teriyaki Hot Smoked Salmon for Undeclared Wheat and Soy

    Jensens Old Fashioned Smokehouse is recalling teriyaki hot smoked salmon products due to undeclared wheat and soy sauce ingredients.

    Product
    Teriyaki hot smoked Atlantic salmon, Teriyaki hot smoked King salmon, Teriyaki hot smoked Sockeye salmon, Teriyaki hot smoked salmon (no species listed). Product was packed in bulk cases, 10 lbs. each, sold in bulk bin. There are no retail packages and NO UPC.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0978-2016·2016-04-13

    Bj's Wholesale Club Recalls Deli Sliced Pastrami for Cross-Contact Risk

    Bj's Wholesale Club is recalling deli-sliced pastrami that may have been cut on equipment used for mortadella with pistachios, posing a potential allergen exposure risk.

    Product
    WF PASTRAMI, sold in a deli bag. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1273-2016·2016-04-13

    Focus Diagnostics Recalls Simplexa Direct Amplification Discs for Diagnostic Errors

    Focus Diagnostics is recalling Simplexa Direct Amplification Discs because they may cause false test results or error codes.

    Product
    Simplexa Flu A/B & RSV Direct (MOL2650) with Direct Amplification Disc (MOL1451, MOL1452, MOL1455) Model Number: MOL2650, MOL1451, MOL1452, MOL1455
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0968-2016·2016-04-13

    Bj's Recalls Black Forest Ham Sliced on Shared Equipment

    Bj's Wholesale Club is recalling Black Forest Ham sold in deli bags because it may have been sliced on equipment used for mortadella with pistachios.

    Product
    WF Black Forest Ham, sold in a deli bag. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-0939-2016·2016-04-13

    BJ's Recalls D&W Gourmet LITE Turkey Deli Meat

    BJ's Wholesale Club is recalling D&W Gourmet LITE Turkey deli meat sold in eight states due to potential cross-contact with pistachio-containing mortadella.

    Product
    D&W Gourmet LITE Turkey, packaged in deli bag. This is a deli service item.
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-0973-2016·2016-04-13

    Bj's Recalls WF Honey Ham Due to Cross-Contact Risk

    Bj's Wholesale Club is recalling WF Honey Ham deli items that may have been sliced on equipment used for mortadella with pistachios.

    Product
    WF Honey Ham. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1328-2016·2016-04-13

    MicroAire PAL-R4011XL Cannula Recalled Due to Breakage During Surgery

    MicroAire is recalling PAL-R4011XL cannulas because three reports indicated the devices bent or broke during surgical procedures.

    Product
    MicroAire PAL¿ Cannula Product Usage - Power Aspiration Device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0932-2016·2016-04-13

    Bj's Recalls Sriracha Chicken Deli Item for Cross-Contact Risk

    Bj's Wholesale Club is recalling D&W Sriracha Chicken deli items because they may have been sliced on equipment used for pistachio-containing mortadella.

    Product
    D&W SRIRACHA CHICKEN, packaged in deli bag. This is a deli service item.
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1344-2016·2016-04-13

    AngioDynamics Recalls Renown Regional Medical Center Convenience Kits

    AngioDynamics is recalling 100 Renown Regional Medical Center Convenience Kits because the needle inner lumen is too small to accept the intended guidewire.

    Product
    NAMIC CONVENIENCE KIT RENOWN REGIONAL MEDICAL CENTER, REF Catalog No. 65230029, UPN Product No. H965652300290, Product is packed as a box of 30 pieces, box label contains UPN Product No. H965652300291 Product Usage - This needle is intended to be placed over the guidewire to e
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0957-2016·2016-04-13

    BJ's Wholesale Club Recalls Harvestland Roasted Turkey Deli Items

    BJ's Wholesale Club is recalling Harvestland Roasted Turkey deli items that may have been sliced on equipment used for pistachio-containing mortadella.

    Product
    Harvestland Roasted Turkey, sold in a deli bag. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1316-2016·2016-04-13

    Recall of eValueMed Infant Heel Warmers and Transport Mattresses

    Philips is recalling eValueMed Infant Heel Warmers and Transport Mattresses because they lack expiration dates and warnings about overheating risks after shelf life.

    Product
    evaluemed Infant Heel Warmer 301-1223; Distributed by Tri-anim A disposable heel warmer for use when circulation needs to be stimulated in the infant heel in order for blood sampling to occur
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0976-2016·2016-04-13

    Bj's Recalls Oven Honey Chicken Due to Potential Cross-Contact

    Bj's Wholesale Club is recalling Oven Honey Chicken deli items that may have been sliced on equipment used for mortadella with pistachios.

    Product
    WF Oven Honey Chicken, sold in a deli bag. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1346-2016·2016-04-13

    AngioDynamics Recalls NAMIC Convenience Kits Due to Needle Lumen Defect

    AngioDynamics is recalling 45 NAMIC Convenience Kits because the needle inner lumen may be too small to accept a 0.038-inch guidewire.

    Product
    NAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT, REF Catalog No. 601319810, UPN Product No. H7496013198101 Product Usage - This needle is intended to be placed over the guidewire to enlarge the opening in the vessel, and is then removed before sliding the catheter ove
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0991-2016·2016-04-13

    Bj's Recalls Citterio Hard Salami Due to Potential Cross-Contact

    Bj's Wholesale Club is recalling Citterio Hard Salami sold in deli bags because it may have been sliced on equipment used for pistachio mortadella.

    Product
    CITTERIO HARD SALAMI, sold in a deli bag. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-0996-2016·2016-04-13

    BJ's Wholesale Club Recalls Deli Roast Beef Due to Cross-Contact Risk

    BJ's Wholesale Club is recalling 3FT American Substitute Roast Beef sold in eight states because it may have been sliced on equipment used for pistachio mortadella.

    Product
    3FT American Substitute Roast Beef. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1348-2016·2016-04-13

    Ortho-Clinical VITROS 5600 Integrated System Recalled for Wiring Error

    Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems because a wiring error may leave a module energized when the power cord is unplugged.

    Product
    VITROS 5600 Integrated System, Unique Device Identifier No. 10758750002740 & 10758750007110. Intended for use in the in vitro measurement of a variety of analytes of clinical interest.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0980-2016·2016-04-13

    BJ's Wholesale Club Recalls Turkey Deli Slices for Cross-Contact Risk

    BJ's Wholesale Club is recalling deli turkey slices that may have been sliced on equipment used for mortadella with pistachios, posing a potential allergen cross-contact risk.

    Product
    WF Sandwich Ring substitute Turkey. This is a deli service item
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-1039-2016·2016-04-13

    NutraKey Recalls VPro Raw Plant Protein Due to Undeclared Soy

    NutraKey, Inc. is recalling VPro Raw Plant Protein, Chocolate, because it contains undeclared soy. The recall covers 17,730 units distributed nationwide.

    Product
    VPro Raw Plant Protein, Chocolate. Packaged in a plastic bottle with green, white, and black adhesive label. Packaged in 1 lb (15 serving) and 2 lb (30 serving).
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1031-2016·2016-04-13

    Sweetwater Sprouts Recalled for Potential Salmonella Contamination

    Sweetwater Farms LLC is recalling sprouted alfalfa due to potential Salmonella contamination. The product was distributed in Arkansas, Kansas, and Oklahoma.

    Product
    Sweetwater Sprouts 100% Pure Sprouted Alfalfa packaged in the following configurations: 4 oz. plastic bags (UPC 7 56733 00104 2) packed 12 per case; 16 oz. (1 lb.) plastic bags; and 5 lb. bulk boxes The product is shipped in cardboard cases labeled with product and lot n
    Category
    Food
    Distribution
    3 states

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