The Recall Desk

Archive

March 2015 recalls

559 recalls were announced in March 2015.

What the numbers show

Critical
102
Severe
148
High
245
Moderate
50
Low
14

Of the 559 recalls this month scored against our rubric, 18% are Critical, 26% are Severe.

Which agencies issued them

101–200 of 559

  • ModerateFDA (Devices)·Z-1268-2015·2015-03-25

    Med-logics Recalls ML 7090 Calibrated LASIK Blades Due to Fit Issues

    Med-logics Inc is recalling 360 units of ML 7090 Calibrated LASIK Blades because they do not fit into the AMO Amadeus Metal Blade Holder.

    Product
    ML 7090 Calibrated LASIK Blade (CLB); CLB CALIBRATED LASIK BLADE 10. ML 7090 Calibrated LASIK Blade (CLB) is to be used as replacement blades for the AMO Amadeus Microkeratome, to perform lamellar keratectomy procedures.
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-1287-2015·2015-03-25

    Materialise Recalls Signature TKA Surgical Guides Due to Incorrect Patient Images

    Materialise N.V. is recalling Signature TKA GDE/MDL Set 04-05 surgical guides because images from a different patient were used for production.

    Product
    Signature TKA GDE/MDL Set 04-05 (Femur & Tibia) The Signature Patient-Specific Surgical Guides are intended to be used as part of the Signature Personalized Patient Care System. Lt is intended to be used as a guide during the surgical procedure for total and partial knee arthr
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1277-2015·2015-03-25

    US Infusion Recalls Medstream IV Sets Due to Leaking

    US Infusion is recalling 62,700 Medstream IV infusion sets because they may leak at the Y site. The sets were distributed in six states.

    Product
    Medstream 81" (206 cm) 20 drop Universal Administration Sets. Disposable IV infusion set with 3 year expiration date.
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1275-2015·2015-03-25

    Bard Access Systems Recalls BD PosiFlush Saline Flush Syringes Due to Open Seals

    Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes included in certain device kits because open seals may compromise product sterility.

    Product
    BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: Groshong Midline Bard MYPICC Kit 4F (Single-Lumen) The syringe is used to pre-flush the catheter prior to placement and may also be used to verify patency post-placement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1452-2015·2015-03-25

    Mi Pepito Ground Shrimp Recalled for Unallowed Dyes and Sulfites

    N.A.C. Foods is recalling Mi Pepito Ground Shrimp in New Jersey and New York due to unallowed dyes and undeclared sulfites.

    Product
    Mi Pepito Camaron Molido Ground Shrimp, Net wt. .75 oz (16 gr), Packaged in a plastic bag, Packed & Distributed by: N.A.C. Corp., Palisades Park, NJ, UPC 707425900051
    Category
    Food
    Distribution
    2 states
  • LowFDA (Devices)·Z-1294-2015·2015-03-25

    LeMaitre Vascular TCI System Recalled for Incorrect Expiration Date Labeling

    LeMaitre Vascular is recalling 54 units of the Tumescent Catheter Inversion System because they were mislabeled with an incorrect expiration date.

    Product
    LeMaitre Vascular Tumescent Catheter Inversion (TCI) System. The TCI System is intended to provide a system to the removal of an incompetent greater saphenous vein. Catalog Number: 7210023, lot #61049252
    Category
    Medical Device
    Distribution
    7 states
  • LowFDA (Devices)·Z-1289-2015·2015-03-25

    Siemens N Latex IgM Reagent Recalled for Proficiency Testing Failures

    Siemens Healthcare Diagnostics is recalling specific lots of N Latex IgM reagents because they failed proficiency testing, resulting in low recovery rates for serum samples.

    Product
    N Latex IgM; In-vitro diagnostic reagent for the quantitative determination of IgM in human cerebrospinal fluid (CSF) and in paired CSF/serum samples by means of particle-enhanced immunonephelometry using the BN II and BN ProSpec Systems. The determination of IgM aids in the eval
    Category
    Medical Device
    Distribution
    7 states
  • LowUSDA FSIS·052-2015·2015-03-25

    Viz Cattle Recalls Flap Meat Beef for Missing Ingredient Labeling

    Viz Cattle is recalling 62,841 pounds of flap meat beef because the product labels lack an ingredient statement. No undeclared allergens or adverse reactions have been reported.

    Product
    Recall Notification Report 052-2015 (Flap Meat Beef)
    Category
    Food
    Distribution
    1 state
  • LowFDA (Drugs)·D-0412-2015·2015-03-25

    Mylan Recalls Doxorubicin Vials Due to Potential Mispackaging

    Mylan Institutional LLC is recalling 936 vials of Doxorubicin Hydrochloride Injection because they may have been mispackaged with Ifosfamide Injection.

    Product
    DOXOrubicin Hydrochloride Injection, USP, 200 mg/100 mL (2 mg/mL), For IV Use Only, Sterile, ISOTONIC SOLUTION, Caution: Cytotoxic Agent, 100 mL Multi-Dose Vial, Rx Only, Manufactured By: Onco Therapies Limited, Bangalore, 560105, INDIA, Distributed By: Amneal-Agila, LLC, Glasgow
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V172000·2015-03-24

    Ford Recalls 2013-2015 Lincoln MKT Vehicles Due to Fire Risk

    Ford is recalling specific 2013-2015 Lincoln MKT vehicles with limousine or hearse packages because a vacuum pump relay may overheat, increasing the risk of a vehicle fire.

    Product
    LINCOLN — LINCOLN MKT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V170000·2015-03-24

    Spartan Recalls 2011-2016 School Bus Chassis Due to Fire Risk

    Spartan Motors is recalling 2011-2016 school bus chassis because fuel system components may melt, causing engine stalls or vehicle fires.

    Product
    SPARTAN — SPARTAN SB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V173000·2015-03-24

    KZ-RV Recalls 723 Recreational Vehicles Due to Failing Entry Step Rivets

    KZ-RV is recalling 723 recreational vehicles because a rivet on the quad entry steps may shear and fail, causing the steps to give and increasing the risk of personal injury.

    Product
    KZ-RV — KZ-RV STONERIDGE, GOLDRUSH DISCOVERY, GOLDRUSH, GOLDRUSH NUGGET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V171000·2015-03-24

    Ford Recalls 2011-2013 Explorers for Door Handle Spring Defect

    Ford is recalling 2011-2013 Explorers because an interior door handle spring may unseat, preventing the handle from returning to its stowed position. This could cause the door to unlatch in a side impact crash.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V168000·2015-03-23

    Navistar Recalls 2015 IC RE Transit Buses for Brake Hose Defect

    Navistar is recalling 2015 IC RE non-school Transit Buses because the front air brake hose may contact the tire, causing leaks and increased crash risk.

    Product
    IC BUS — IC BUS RECB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V165000·2015-03-23

    Navistar Recalls 2015-2016 International Trucks Due to Brake Fire Risk

    Navistar is recalling 2015-2016 International and IC Bus vehicles because defective brake actuators may cause dragging, overheating, and wheel end fires.

    Product
    INTERNATIONAL — INTERNATIONAL, IC BUS TRANSTAR, CE, DURASTAR, WORKSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V166000·2015-03-23

    Navistar Recalls 2015-2016 IC School Buses for Brake Fire Risk

    Navistar is recalling specific 2015-2016 IC school buses because defective air brake actuators may cause dragging brakes and wheel end fires.

    Product
    IC BUS — IC BUS CASB, CESB, RESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V164000·2015-03-23

    GM Recalls 2013-2015 Chevrolet Malibu for Sunroof Pinch Hazard

    General Motors is recalling 2013-2015 Chevrolet Malibus because the sunroof switch may be pressed inadvertently, causing the roof to close unexpectedly and risk pinch injuries.

    Product
    CHEVROLET — CHEVROLET MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·051-2015·2015-03-23

    Stock Yards Meat Packing Recalls Mislabeled Roast Beef Product

    Stock Yards Meat Packing Co. is recalling approximately 2,149 pounds of roast beef mistakenly labeled as corned beef. The product was shipped to businesses in Arizona and California.

    Product
    Stock Yards Meat Packing Co., Inc. Recalls Roast Beef Product Due to Misbranding
    Category
    Food
    Distribution
    2 states
  • CriticalUSDA FSIS·049-2015·2015-03-20

    Van Lang Foods Recalls Pork and Chicken Products for Undeclared Egg

    Van Lang Foods is recalling pork potstickers and chicken dim sum because they contain egg, a known allergen not listed on the label.

    Product
    Van-Lang Enterprises, Inc. — Van Lang Foods Recalls Pork And Chicken Products Due To Misbranding And Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·15V160000·2015-03-20

    Forest River Recalls 2013-2014 Sabre Trailers Due to Brake Wiring Defect

    Forest River is recalling 2013-2014 Sabre travel trailers and fifth wheels because improperly routed brake wires may chafe, break, or short, increasing crash and fire risks.

    Product
    FOREST RIVER — FOREST RIVER SABRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V159000·2015-03-20

    Charles Machine Recalls Ditch Witch T26 Trailers Due to Bearing Defect

    Charles Machine is recalling 2002-2015 Ditch Witch T26 trailers because incorrect wheel bearings may fail, causing the wheel to detach and increasing crash risk.

    Product
    CHARLES MACHINE — CHARLES MACHINE DITCH WITCH T26
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·050-2015·2015-03-20

    Boa Vida Imports Recalls Pork and Beef Products from Portugal

    Boa Vida Imports is recalling pork and beef products imported from Portugal without inspection because the country is ineligible to export meat to the U.S.

    Product
    Boa Vida Imports Recalls Pork And Beef Products Imported From An Ineligible Country Without Benefit Of Import Inspection
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·15V162000·2015-03-20

    GM Recalls 2015 Buick Encore and Chevrolet Trax for Tire Label Defect

    General Motors is recalling 2015 Buick Encore and Chevrolet Trax vehicles because tire placards lack rim size information, which may lead to incorrect rim replacement and increased crash risk.

    Product
    CHEVROLET — CHEVROLET, BUICK TRAX, ENCORE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V161000·2015-03-20

    Jerr-Dan Recalls 2010 Standard Duty Wreckers Due to Boom Drift Risk

    Jerr-Dan is recalling 50 model year 2010 Standard Duty Wreckers because the underlift boom may drift down during towing, increasing the risk of a crash.

    Product
    JERR-DAN — JERR-DAN STANDARD DUTY WRECKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·15102·2015-03-19

    Residential Elevators Recalled Due to Crushing Hazard and Brain Injury

    CPSC recalls Elmira Hydraulic residential elevators sold by Coastal Carolina Elevators because the gate door can open while operating, causing a crushing hazard.

    Product
    Residential hydraulic elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1395-2015·2015-03-18

    First Spice Mixing Recalls Karl's Hot Chorizo Seasoning Due to Peanut Contamination

    First Spice Mixing Co. is recalling specific lots of Karl's Hot Chorizo Seasoning because ground cumin may be contaminated with undeclared peanut protein.

    Product
    KARL'S HOT CHORIZO SEASONING R-1 (CH0-015), Net Weight XXXX Lbs. -- FIRST SPICE MIXING COMPANY LONG ISLAND CITY, N.Y. --- INGREDIENTS: SALT, PAPRIKA, SPICES, GARLIC POWDER, FLAVORING (SPICE EXTRACTIVES). NO MORE THAN 2% PROPYLENE GLYCOL AS ANTI-CAKING AGENT. --- The % of cumin u
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1412-2015·2015-03-18

    Chili Powder Recalled for Undeclared Peanut Protein

    Wm. E. Martin & Sons Co., Inc. is recalling 50-pound bags of chili powder because they contain undeclared peanut protein.

    Product
    CHILI POWDER 50 LBS
    Category
    Food
    Distribution
    14 states
  • CriticalFDA (Food)·F-1388-2015·2015-03-18

    First Spice Mixing Recalls Ground Cumin for Undeclared Peanut

    First Spice Mixing Co. is recalling specific lots of pure ground cumin because they may contain undeclared peanut protein.

    Product
    PURE GROUND CUMIN, Net Weight XXX Lbs. -- FIRST SPICE MIXING COMPANY - LONG ISLAND CITY, N. Y.
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1406-2015·2015-03-18

    Korean Food Co. Recalls Soybean Sprouts Due to Listeria Risk

    Korean Food Co. is recalling specific bags of soybean spruts sold in Texas because they may be contaminated with Listeria monocytogenes.

    Product
    SOYBEAN SPROUTS Go-Hang Net Wt. 1 LBS.and 2 LBS.(Keep Refrigerated) TEL: (972)790-4800 1311LUKEST IRVING. TX.75061 Korean Food Co.; SOYBEAN SPROUTS Go-Hang NET. WT 10 LBS. (KEEP REFRIGERATED) Korean Food Grop 1311 LUKEST IRVING. TX.75061
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1396-2015·2015-03-18

    First Spice Mixing Recalls Pinata's Asada Seasoning for Undeclared Peanut

    First Spice Mixing Co. is recalling Pinata's Asada Seasoning because it may contain undeclared peanut protein, posing a risk to individuals with peanut allergies.

    Product
    PINATA'S ASADA SEASONING (SEA-164), Net Weight XXXX Lbs. -- FIRST SPICE MIXING COMPANY LONG ISLAND CITY, N.Y. --- INGREDIENTS: SALT, SPICES, SUGAR, CITRIC ACID, DEHYDRATED GARLIC, PAPRIKA, NATURAL SMOKE, OIL OF LIME. --- The % of cumin used in the finished seasoning mix is 3.30%
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1399-2015·2015-03-18

    First Spice Mixing Company Recalls Salsa Pica Asada for Undeclared Peanut

    First Spice Mixing Company is recalling specific lots of Salsa Pica Asada because ground cumin ingredients may contain undeclared peanut protein.

    Product
    SALSA PICA ASADA (SEA-268), Net Weight XXXX Lbs. -- FIRST SPICE MIXING COMPANY LONG ISLAND CITY, N.Y. --- INGREDIENTS: SALT, SPICES, SUGAR, PAPRIKA, CITRIC ACID, GARLIC POWDER, DEHYDRATED ONION. --- The % of cumin used in the finished seasoning mix is 4.50%. --- The affected lo
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1387-2015·2015-03-18

    Julian Bakery Recalls Paleo Protein Bars for Undeclared Cashews

    Julian Bakery is recalling Paleo Protein Bars in Chocolate Brownie and Cookies N' Creme flavors due to undeclared cashews.

    Product
    Paleo Protein Bar Cookies N' Creme NET WT. 2.1OZ (60G) Manufactured by Julian Bakery, Inc. Developed by Paleo, Inc. GMO-Free, Gluten-Free, No Sugar Alcohols Ingredients: Egg Whites, Isomalto-Olgosaccharide (Prebiotic Fiber), Organic Sunflower Seeds, Chocolate, Water, Col
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1391-2015·2015-03-18

    First Spice Mixing Recalls Burrito Loco Seasoning for Peanut Allergen

    First Spice Mixing Co. is recalling specific lots of Burrito Loco All-Purpose Seasoning because ground cumin ingredients may contain undeclared peanut protein.

    Product
    BURRITO LOCO ALL-PURPOSE SEASONING (SEA-189) -- FIRST SPICE MIXING COMPANY LONG ISLAND CITY, N.Y. --- INGREDIENTS: SALT, HYDROLYZED SOY PROTEIN, SUGAR, SPICES, FLAVORINGS (SPICE EXTRACTIVES). --- The % of cumin used in the finished seasoning mix is 0.75%. --- The affected lots we
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1398-2015·2015-03-18

    First Spice Mixing Recalls Rieker Grill & Braten for Peanut Allergen

    First Spice Mixing Co. is recalling Rieker Grill & Braten seasoning because ground cumin may contain undeclared peanut protein.

    Product
    RIEKER GRILL & BRATEN (SAU-048), Net Weight XXXX Lbs. -- FIRST SPICE MIXING COMPANY LONG ISLAND CITY, N.Y. --- INGREDIENTS: SALT, SPICES, PAPRIKA, MONOSODIUM GLUTAMATE, ONION POWDER, GARLIC POWDER. --- The % of cumin used in the finished seasoning mix is 0.50%. --- The affected
    Category
    Food
    Distribution
    7 states
  • CriticalUSDA FSIS·048-2015·2015-03-18

    StoneRidge Recalls Pork Tenderloin Due To Undeclared Milk Allergen

    StoneRidge Wholesale Division LLC is recalling pork tenderloin products because they contain undeclared milk, a known allergen.

    Product
    StoneRidge Wholesale Division LLC — Stoneridge Wholesale Division, LLC Recalls Pork Tenderloin Product Due To Misbranding And Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1394-2015·2015-03-18

    First Spice Mixing Recalls Green Cactus Spicy Special Seasoning for Peanut Allergen

    First Spice Mixing Co. is recalling Green Cactus Spicy Special Seasoning because it may contain undeclared peanut protein.

    Product
    GREEN CACTUS SPICY SPECIAL SEASONING (SEA-903), Net Weight XXXX Lbs. -- FIRST SPICE MIXING COMPANY LONG ISLAND CITY, N.Y. --- INGREDIENTS: SALT, SUGAR, SPICES, PAPRIKA, ONION POWDER, GARLIC POWDER, CORN STARCH, LESS THAN 2% CALCIUM SILICATE AS AN ANTI-CAKING AGENT. --- The % of
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1401-2015·2015-03-18

    First Spice Mixing Recalls Taco Seasoning for Undeclared Peanut

    First Spice Mixing Co. is recalling Taco Perfectos All-Purpose Seasoning because it may contain undeclared peanut protein.

    Product
    TACO PERFECTOS ALL-PURPOSE SEASONING (SEA-323), Net Weight XXXX Lbs. -- FIRST SPICE MIXING COMPANY LONG ISLAND CITY, N.Y. --- INGREDIENTS: SALT, HYDROLYZED SOY PROTEIN, SUGAR, SPICES, FLAVORINGS (SPICE EXTRACTIVES). ALLERGEN: CONTAINS SOY. --- The % of cumin used in the finished
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1392-2015·2015-03-18

    First Spice Mixing Recalls Hot Southwestern Seasoning for Peanut Contamination

    First Spice Mixing Co. is recalling 24,000 lbs of Worthington Hot Southwestern Seasoning II-B because it may contain undeclared peanut protein.

    Product
    WORTHINGTON HOT SOUTHWESTERN SEASONING II- B, Net Weight 50 Lbs. -- FIRST SPICE MIXING COMPANY LONG ISLAND CITY, N. Y. --- INGREDIENTS: SPICES, ONION POWDER, GARLIC POWDER, PAPRIKA, LEMON EXTRACT. --- The % of cumin used in the finished seasoning mix is 4.0%. --- The affected
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1397-2015·2015-03-18

    First Spice Mixing Recalls Asada Seasoning Due to Undeclared Peanut

    First Spice Mixing Co. is recalling Pinata's Asada Seasoning R-1 because it may contain undeclared peanut protein. The product was distributed in seven states.

    Product
    PINATA'S ASADA SEASONING R-1 (BBQ-140), Net Weight XXXX Lbs. -- FIRST SPICE MIXING COMPANY LONG ISLAND CITY, N.Y. --- INGREDIENTS: SALT, TURBINADO SUGAR, BROWN SUGAR, SPICES, DEHYDRATED GARLIC AND ONION, PAPRIKA. --- The % of cumin used in the finished seasoning mix is 1.70%. --
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1411-2015·2015-03-18

    Ground Cumin Recalled for Undeclared Peanut Protein

    Wm. E. Martin & Sons Co. is recalling 396 units of ground cumin due to undeclared peanut protein. The product was distributed to 14 states.

    Product
    GROUND CUMIN STERILE TREATED PROD. OF TURKEY, 50 LBS.
    Category
    Food
    Distribution
    14 states
  • CriticalFDA (Food)·F-1389-2015·2015-03-18

    First Spice Mixing Recalls Andouille Sausage Seasoning for Undeclared Peanut

    First Spice Mixing Co. is recalling specific lots of Ehmer Cooked Andouille Sausage Seasoning because ground cumin may contain undeclared peanut protein.

    Product
    EHMER COOKED ANDOUILLE SAUSAGE SEASONING (AND-119), Net Weight XXX Lbs. -- INGREDIENTS: SALT, BROWN SUGAR, SPICES, PAPRIKA, DEHYDRATED GARLIC, OLEORESIN PAPRIKA AND SPICE EXTRACTIVES. FIRST SPICE MIXING COMPANY NEW YORK --- The % of cumin used in the finished seasoning product
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1413-2015·2015-03-18

    Soyko International Recalls Non-GMO Soybeans for Sprouting Due to Listeria

    Soyko International is recalling Non-GMO soybeans for sprouting because FDA testing found Listeria monocytogenes. The affected product was distributed in Texas.

    Product
    Byglands, Non-GMO soybeans for Sprouting in 25KG bags and 1MT tote bags.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1390-2015·2015-03-18

    First Spice Mixing Recalls Seasoning for Undeclared Peanut Allergen

    First Spice Mixing Co. is recalling specific lots of Blue Tortilla All-Purpose Seasoning because ground cumin ingredients may contain undeclared peanut protein.

    Product
    BLUE TORTILLA ALL-PURPOSE SEASONING R-1 (SEA-188), Net Weight XXX Lbs. -- FIRST SPICE MIXING COMPANY LONG ISLAND CITY, NEW YORK -- INGREDIENTS: SALT, HYDROLYZED SOY PROTEIN, SUGAR, SPICES, FLAVORINGS (SPICE EXTRACTIVES). ALLERGEN: CONTAINS SOY. --- The % of cumin used in the fini
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Devices)·Z-1249-2015·2015-03-18

    Microport Evolution Tibial Base Recalled for Casting Tool Defect

    Microport Orthopedics is recalling 17 units of the Evolution Tibial Base knee prosthesis component due to a casting tool issue causing varying retaining wall thickness and keel offset.

    Product
    EVOLUTION MP TIBIAL BASE, REF ETPKN8SR, SIZE 8 RIGHT, TYPE PRIMARY, FIT CEMENTED, STYLE KEELED, STERILE R, Rx ONLY, MicroPort Orthopedics, Inc. Knee prosthesis component.
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-1247-2015·2015-03-18

    Arjo Pressure IQ Evolve Mattress Recalled for Pressure Ulcer Risk

    Arjo is recalling 1,034 Pressure IQ Evolve mattresses nationwide due to failures that resulted in pressure ulcers.

    Product
    Pressure IQ Evolve Mattress; Non-powered mattress replacement system. Intended for patients with medium to high risk for developing pressure ulcers while on a mattress.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1251-2015·2015-03-18

    Philips DuraDiagnost X-Ray System Recalled for Installation Defects

    Philips Medical Systems is recalling 71 DuraDiagnost X-Ray systems worldwide due to improper installation risks that could cause equipment to fall or float.

    Product
    Philips DuraDiagnost X-Ray system, Stationary X-Ray System Radiographic Models: 712210, 712211
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-1386-2015·2015-03-18

    Julian Bakery Recalls Paleo Protein Bars Due to Undeclared Cashews

    Julian Bakery is recalling Paleo Protein Bars because they contain undeclared cashews, a major allergen.

    Product
    Paleo Protein Bar Chocolate Brownie NET WT. 2.1OZ (60G) GMO-Free, Gluten-Free, No Sugar Alcohols Ingredients: Egg (White Protein, Isomalto-Olgosaccharide (Prebiotic Fiber), Organic Sunflower Seeds, Coconut Oil, Cold Presses Organic Palm Oil, Chocolate, Water, Vanilla, Ora
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1400-2015·2015-03-18

    Taco Hut Enchilada Sauce Base Seasoning Recalled for Undeclared Peanut

    First Spice Mixing Co. is recalling Taco Hut Enchilada Sauce Base Seasoning because it may contain undeclared peanut protein.

    Product
    TACO HUT ENCHILADA SAUCE BASE SEASONING (ENC--101), Net Weight XXXX Lbs. -- FIRST SPICE MIXING COMPANY LONG ISLAND CITY, N.Y. --- INGREDIENTS: WHEAT FLOUR, SALT, SUGAR, SPICES, GARLIC POWDER, HYDROLYZED SOY PROTEIN, ONION POWDER, MONOSODIUM GLUTAMATE, CARAMEL POWDER, OLEORESIN P
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1402-2015·2015-03-18

    First Spice Mixing Recalls Vallarta's Asada R-1 for Undeclared Peanut

    First Spice Mixing Co. is recalling Vallarta's Asada R-1 seasoning due to potential peanut contamination not listed on the label.

    Product
    VALLARTA'S ASADA R-1 (SEA-230), Net Weight XXXX Lbs. -- FIRST SPICE MIXING COMPANY LONG ISLAND CITY, N.Y. --- INGREDIENTS: SALT, SUGAR, CITRIC ACID, SPICES, DEHYDRATED GARLIC, PAPRIKA, DEHYDRATED TOMATO, NATURAL SMOKE, LIME OIL. --- The % of cumin used in the finished seasonin
    Category
    Food
    Distribution
    7 states
  • SevereNHTSA·15V157000·2015-03-18

    GM Recalls 2015 Chevrolet Colorado and GMC Canyon for Air Bag Defect

    General Motors is recalling 2015 Chevrolet Colorado and GMC Canyon vehicles because the driver's air bag inflator may be misaligned, posing a risk of injury during deployment.

    Product
    CHEVROLET — CHEVROLET, GMC COLORADO, CANYON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V156000·2015-03-18

    Forest River Recalls 2014 Palomino SolAire Trailers Due to Furnace Vent Defect

    Forest River is recalling 2014 Palomino SolAire trailers manufactured between July and August 2014 because they may lack an exterior furnace vent, posing risks of carbon monoxide poisoning and fire.

    Product
    FOREST RIVER — FOREST RIVER PALOMINO SOLAIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0410-2015·2015-03-18

    Fusion Pharmaceuticals Recalls Contaminated Diphenhydramine Oral Suspension Kits

    Fusion Pharmaceuticals is recalling 9,439 kits of Dicopanil oral suspension due to microbial contamination with Burkholderia multivorans. The affected kits were distributed in California.

    Product
    DICOPANOL (diphenhydramine hydrochloride in 5 mg/mL oral suspension kit) FusePaq, 150 mL Kits, Rx Only. Fusion Pharmaceuticals LLC., 768 Calle Plano, Camarillo, CA 93012. NDC: 43093-104-01.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-1415-2015·2015-03-18

    CSM Bakery Recalls Frozen Cookie Dough Due to Undeclared Peanuts

    CSM Bakery Products is recalling frozen unbaked cookie dough because it contains undeclared peanuts. The product was distributed to 14 states.

    Product
    TranSmart Raspberry Filled frozen unbaked cookie dough, 108/1.75 oz. units, CSM Bakery Products, 3301 Montreal Industrial Way Tucker, GA 30084..
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-1250-2015·2015-03-18

    Pivotal Health Solutions Recalls Apollo Laser Desktop Control Units

    Pivotal Health Solutions is recalling 35 Apollo Laser Desktop Control Units because internal mounting kits do not meet safety standards, increasing the risk of electric shock.

    Product
    Apollo (cold) Laser Desktop Control Units, Model AP2-DT. The Apollo IR Heat Lamp System is intended to emit energy in the infrared spectrum to provide topical heating for the purpose of elevating tissue temperature for the temporary relief of minor muscle and joint pain and st
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Food)·F-1403-2015·2015-03-18

    Gonnella Baking Recalls Jewel Gourmet Sandwich Rolls for Undeclared Milk

    Gonnella Baking Co. is recalling Jewel brand Gourmet Sandwich Rolls because they contain undeclared milk (whey). The product was distributed in Illinois, Indiana, and Wisconsin.

    Product
    Gourmet Sandwich Rolls sold under the Jewel brand and packaged with 8 rolls to a 20 oz. plastic transparent bag.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1248-2015·2015-03-18

    GE Healthcare Recalls Proteus XR/a X-ray Systems Due to Cable Breakage Risk

    GE Healthcare is recalling Proteus XR/a X-ray systems because a steel cable supporting the bucky device may break. A falling bucky could injure a patient or operator.

    Product
    GE Healthcare Proteus XR/a with wall stand model number 2260354. Intended for use in generating radiographic images of human anatomy in all general purpose diagnostic procedures. This device is not intended for mammographic applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1405-2015·2015-03-18

    Dr. Praeger's Bombay Curry Veggie Burgers Recalled for Peanut Contamination

    Ungar's Food Products is recalling Dr. Praeger's Bombay Curry Veggie Burgers because a cumin ingredient tested positive for peanut protein.

    Product
    Dr. Praeger's Sensible Foods Bombay Curry Veggie Burgers 11 oz retail box Manufactured by Dr. Praeger's Sensible Foods Elmwood Park, NJ 07047 www.drpraegers.com Made in the USA UPC 80868 00050
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-1079-2015·2015-03-18

    Villa Radiology Juno DFR X-ray System Recalled for Control Defects

    Villa Radiology Systems LLC is recalling 30 Juno DFR X-ray systems because they lack required audible signals, permanent activation, and manual override features.

    Product
    Juno DFR X-ray system
    Category
    Medical Device
    Distribution
    21 states
  • HighFDA (Devices)·Z-1256-2015·2015-03-18

    Siemens Healthcare Recalls Capillary Caps Due to Breakage Risk

    Siemens Healthcare is recalling capillary caps for RAPIDLyte blood collection devices because they may not attach properly, causing glass capillaries to break.

    Product
    Siemens Healthcare Caps for capillary 100 uL , Package count 200 For use with blood collection Multicap glass and Multicap-S plastic capillaries SMN: 10311053 Legacy Part number: 478601
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V158000·2015-03-18

    Charles Machine Recalls Ditch Witch T18 Trailers Due to Wheel Lockup Risk

    Charles Machine is recalling 2013-2015 Ditch Witch T18 trailers because incorrect bearing pre-loads may cause wheels to lock up, increasing crash risk.

    Product
    CHARLES MACHINE — CHARLES MACHINE DITCH WITCH T18
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1260-2015·2015-03-18

    Synthes Inserter for Titanium Elastic Nails Recalled for Mechanical Failure

    Synthes, Inc. is recalling Inserter for Titanium Elastic Nails due to potential mechanical failures including shaft breakage and chuck malfunction.

    Product
    Synthes Inserter for Titanium Elastic Nails; The Inserter for Titanium Elastic Nails (TEN) is intended for fixation of diaphyseal fractures where the canal is narrow or flexibility of the implant is paramount. This includes: lower extremity fractures in pediatric and small-statu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1414-2015·2015-03-18

    La Centro Americana Ground Cumin Recalled for Undeclared Peanut

    La Centro Americana Corporation is recalling 5-pound containers of ground cumin because the product may contain undeclared peanut protein.

    Product
    La Centro Americana COMINO MOLIDO Ground Cumin, Net Wt. 5 LBS held in clear plastic containers. Distributed by: La Centro Americana Corp. 2280 Union Blvd. Bay Shore, NY 11706 Tel. (631) 206-3097
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·15C001000·2015-03-18

    Graco Recalls Child Seats Due to Missing Instruction Manual Label

    Graco is recalling specific child seats manufactured in 2014-2015 because they lack a label indicating where to find the instruction manual, potentially leading to improper use.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15E022000·2015-03-18

    Woodstock Stop Arms Recalled for Non-Compliant Border Width

    Woodstock Safety Mirror Co. is recalling specific Stop Arms because the border width is too narrow, reducing visibility and failing federal safety standards.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1393-2015·2015-03-18

    First Spice Mixing Recalls Esposito Mild Chorizo Seasoning for Peanut Allergen

    First Spice Mixing Co. is recalling Esposito Mild Chorizo seasoning because it may contain undeclared peanut protein. The product was distributed in seven states.

    Product
    ESPOSITO MILD CHORIZO (CHO-122), Net Weight XXXX Lbs. -- FIRST SPICE MIXING COMPANY LONG ISLAND CITY, N.Y. --- INGREDIENTS: SALT, PAPRIKA, SPICES, DEHYDRATED GARLIC, EXTRACT OF PAPRIKA, LESS THAN 2% PROPYLENE GLYCOL AS ANTI-CAKING AGENT. --- The % of cumin used in the finished
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1267-2015·2015-03-18

    Siemens CT System Recalled for Image Artifacts and Safety Issues

    Siemens Medical Solutions is recalling 12 SOMATOM Force CT systems due to potential image artifacts and safety-related software issues.

    Product
    SIEMENS SOMATOM Force with software version VA50A and /or VA50A_FP1 and/or VA50A_SP0; Computed tomography system. Product Usage: The intended use of computed tomography is to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data f
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1410-2015·2015-03-18

    Strawberry Tray Recalled for Undeclared Egg and Soy Allergens

    Real Foods of Seattle is recalling strawberry trays with Devonshire dip due to the addition of an incorrect dressing containing undeclared egg and soy.

    Product
    Product labeling is on the bottom of the container. Label reads in part "SMALL HEART STRAWBERRY TRAY WITH DEVONSHIRE DIP***Use By: 02/16/15 Net Weight 1.5# ***KEEP REFRIGERATED***" Product is packaged in a non flex plastic heart shaped container which is pink on the bottom an
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1261-2015·2015-03-18

    Dako Automated Slide Stainers Recalled for Potential Diagnostic Errors

    Dako North America Inc. is recalling four models of automated slide stainers because a defect may cause buffer leakage, leading to false negative diagnostic results.

    Product
    Autostainer Link 48 (AS480), Autostainer Plus Link Instrument (AS100), Autostainer (S3400), and Autostainer Plus (S3800). Automated slide stainer for in vitro diagnostic use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1266-2015·2015-03-18

    Zimmer Persona Trabecular Metal Tibial Plate Recall for Loosening Complaints

    Zimmer, Inc. is recalling Persona Trabecular Metal Tibial Plates due to increased complaints of loosening and radiolucent lines.

    Product
    Persona Trabecular Metal Tibial Plate / Persona TM Tibia-Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer For use in either posterior cruciate retaining or sacrificing surgical procedures.
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-1262-2015·2015-03-18

    Medela Recalls Sterile Enteral Feeding Syringes Due to Packaging Breach

    Medela Inc. is recalling sterile enteral feeding syringes because a potential packaging breach may have compromised their sterility.

    Product
    - NTL-30 30ml Nutrio Enteral Feeding Syringe (sterile) - NTL-60 60ml Nutrio Enteral Feeding Syringe (sterile) - TL-INT-60 60ml Nutrio Enteral Feeding Syringe with Twistlok adapter (sterile) - INT-60 60mL Nutrio Intopo Enteral Feeding Syringe (sterile) - NGF-60 60ml Nutrio Gra
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1259-2015·2015-03-18

    Arrow Intra-Aortic Balloon Catheter Kit Recalled for Potential Helium Leak

    Arrow International Inc is recalling 166 units of Intra-Aortic Balloon Catheter Kits due to a potential leak that allows helium to escape.

    Product
    Arrow Intra-Aortic Balloon Catheter Kit Fiberoptix (IAB), 8 Fr 40 cc Model: IAB-05840-LWS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1258-2015·2015-03-18

    Siemens Healthcare Recalls Capillary Caps Due to Breakage Risk

    Siemens Healthcare is recalling capillary caps that may fail to attach, causing glass capillaries to break.

    Product
    Siemens Healthcare Caps for capillary 50/60 uL, Package count 200 For use with blood collection Multicap glass and Multicap-S plastic capillaries SMN: 10328655 Legacy Part number: 478527
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1257-2015·2015-03-18

    Siemens Healthcare Recalls Capillary Caps Due to Breakage Risk

    Siemens Healthcare is recalling capillary caps that may fail to attach, causing glass capillaries to break.

    Product
    Siemens Healthcare Caps for capillary 140/175 uL, Package count 100 For use with blood collection Multicap glass and Multicap-S plastic capillaries SMN: 10311054 Legacy Part number: 478605
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1404-2015·2015-03-18

    Gonnella Sub Buns Recalled for Undeclared Milk Allergen

    Gonnella Baking Co. is recalling Sub Buns due to an undeclared milk allergen (whey). The product was distributed in Illinois, Indiana, and Wisconsin.

    Product
    Sub Buns sold under the Gonnella brand and packaged with 8 buns to a 20 oz. plastic transparent bag.
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1252-2015·2015-03-18

    Siemens RAPIDPoint 405 Blood Gas Analyzer Recalled for Neonatal Bilirubin Variability

    Siemens is recalling 3,420 RAPIDPoint 405 Blood Gas Analyzers worldwide because the neonatal bilirubin parameter may show increased variability under specific high-concentration conditions.

    Product
    RAPIDPoint 405 Blood Gas Analyzer; Siemens Material Number: 10310464, 10322347, 10314817, 10317193, 10318999, 10320055, 10322347, 10328278, 10328302, 10336784. These systems are intended for near-patient and laboratory testing of blood gases, electrolytes, metabolites, total
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1253-2015·2015-03-18

    Siemens RAPIDPoint 500 Blood Gas Analyzer Recalled for Neonatal Bilirubin Variability

    Siemens is recalling 4,376 RAPIDPoint 500 Blood Gas Analyzers worldwide because the neonatal bilirubin parameter may show increased variability under specific high-concentration conditions.

    Product
    RAPIDPoint 500 Blood Gas Analyzer; Siemens Material Number: 10492730, 10696855, 10696857, 10697306. The RAPIDPoint 500 system is designed for professional use in a point-of-care or laboratory environment. This system tests blood gases, electrolytes, metabolites, total hemoglo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1254-2015·2015-03-18

    Siemens RapidLab 1245 System Recalled for Neonatal Bilirubin Variability

    Siemens is recalling 241 RapidLab 1245 systems because the neonatal bilirubin parameter may show increased variability under specific high-concentration conditions.

    Product
    RAPIDLab 1245 System; Siemens Material Number: 10321844, 10491393, 10337179. The Rapidlab 1200 systems are intended for in vitro diagnostic use by healthcare professionals in the quantitative testing of human whole blood. The systems can determine the following parameters: RA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1265-2015·2015-03-18

    Southern Implants Recalls Dental Implants Due to Labeling Mismatch

    Southern Implants, Inc. is recalling 130 units of MAX-TL and Z-MAX dental implants because the labeled packages contained the wrong implant type.

    Product
    MAX-TL 9.0 x 7.0 mm Implant, Catalog No. 15711K; Z-MAX Implant 9.0 x 7 mm Length, Catalog No. Z-MAX9-7. Dental implant. Product Usage: The MAX Implant is intended to be implanted in the upper and lower jaw arches to provide support for fixed or removable dental prostheses
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1255-2015·2015-03-18

    Siemens RAPIDLab 1265 System Recalled for Neonatal Bilirubin Variability

    Siemens Healthcare Diagnostics Inc is recalling 2,863 RAPIDLab 1265 Systems because the neonatal bilirubin parameter may show increased variability under specific high-concentration conditions.

    Product
    RAPIDLab 1265 System; Siemens Material Number: 10491395, 10321852, 10335524. The Rapidlab 1200 systems are intended for in vitro diagnostic use by healthcare professionals in the quantitative testing of human whole blood. The systems can determine the following parameters: RA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0408-2015·2015-03-18

    Micro Labs Recalls Simvastatin Tablets Due to Impurity Failure

    Micro Labs USA Inc. is recalling Simvastatin Tablets, 40mg, because the product failed a known impurity specification. The recall affects 13,488 bottles distributed nationwide.

    Product
    Simvastatin Tablets, USP, 40mg, Rx Only, 90 count bottles, Manufactured by: Micro Labs Limited Goa-403 722, India, Manufactured for: Micro Labs USA Inc., Princeton, NJ 08540 NDC 42571-0040-90.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1409-2015·2015-03-18

    Similac Advance Infant Formula Recalled for Chinese Labeling

    Abbott Laboratories is recalling Similac Advance infant formula because export-bound product with Chinese labeling was distributed in the US.

    Product
    Similac¿ Advance Complete Nutrition Infant Formula with Iron, 1.45lb plastic container.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1263-2015·2015-03-18

    Ortho-Clinical VITROS Hand-held Barcode Scanner Recall for Sample Skipping

    Ortho-Clinical Diagnostics is recalling VITROS Hand-held Barcode Scanners because they may skip sample cup positions when using the Batch Programming option.

    Product
    VITROS Hand-held Barcode Scanner, Catalog Number 6844210, for use with the following VITROS Systems: VITROS 5,1 FS Chemistry System, VITROS 3600 Immunodiagnostics System, VITROS 4600 Chemistry System, VITROS 5600 Integrated System. This product is an accessory for use with VITRO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0409-2015·2015-03-18

    Micro Labs Recalls Simvastatin Tablets Due to Impurity Failure

    Micro Labs USA Inc. is recalling 13,464 bottles of Simvastatin 80mg tablets because the product failed a known impurity specification.

    Product
    Simvastatin Tablets, USP, 80mg, Rx Only, 90 count bottles, Manufactured by: Micro Labs Limited Goa-403 722, India, Manufactured for: Micro Labs USA Inc., Princeton, NJ 08540 NDC 42571-080-90.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0411-2015·2015-03-18

    Qualitest Recalls Promethazine DM Syrup Due to Plastic Particulates

    Qualitest Pharmaceuticals is recalling 972 bottles of Promethazine DM Syrup because plastic cap closure particulates may be present in the product.

    Product
    PROMETHAZINE DM SYRUP (Promethazine Hydrochloride, USP and Dextromethorphan Hydrobromide, USP), EACH 5 ml (ONE TEASPOONFUL) CONTAINS: Promethazine Hydrochloride 6.25 mg, Dextromethorphan Hydrobromide 15 mg, alcohol 7%, ONE PINT (574 mL), Rx only, Manufactured for: QUALITEST PH
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0407-2015·2015-03-18

    Micro Labs Recalls Simvastatin Tablets Due to Impurity Failure

    Micro Labs USA Inc. is recalling specific lots of Simvastatin Tablets, 20mg, because the product failed a known impurity specification.

    Product
    Simvastatin Tablets, USP, 20mg a) 90- count bottle (42517-0020-10), b) 1000-count-bottle (NDC 42571-0020-10), Rx only, Manufactured by: Micro Labs Limited Goa-403 722, India, Manufactured for: Micro Labs USA Inc.,Princeton, NJ 08540
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1264-2015·2015-03-18

    Richard-Allan Scientific Recalls Mislabelled CYTO-STAIN R Stain Bottles

    Richard-Allan Scientific is recalling 132 gallons of CYTO-STAIN R Stain because the bottles were incorrectly labeled as CYTO-STAIN G, although the contents are correct.

    Product
    Carton: Richard-Allan Scientific CYTO-STAIN; REF 7501R; Quantity: 1x1 Gallon; Size: 1 Gallon/3.8L; LOT 313833; 11/2016; Bottle: Richard-Allan Scientific CYTO-STAIN G; REF 7501G; 1 Gallon/3.8L; Thermo Scientific.
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Food)·F-1408-2015·2015-03-18

    Keystone Food Products Recalls Veggie Sticks and Straws Due to Labeling Error

    Keystone Food Products is recalling specific brands of veggie sticks and straws because the sodium content listed on the label is incorrect.

    Product
    Weis Veggie Sticks Net Wt. 6 oz. Packed For Weis Markets, Inc. Sunbury, PA 17801 With code dates: 10 Dec 2014 thru 7 Apr 2015 Natures Place Veggie Straws Net Wt. 6 oz Distributed By: DZA Brands, LLC, Salisbury NC 28147/Scarborough, ME 04074 With code dates: 6 Jan 2015
    Category
    Food
    Distribution
    8 states
  • LowFDA (Food)·F-1407-2015·2015-03-18

    Keystone Food Products Recalls Veggie Chips for Incorrect Sodium Labeling

    Keystone Food Products Inc. is recalling specific brands of veggie chips because the sodium content on the label is incorrect. The product contains approximately 290 mg of sodium per serving, not the 55 mg claimed.

    Product
    Weis Veggie Chips Net Wt. 6 oz. Packed For Weis Markets, Inc. Sunbury, PA 17801 With code dates: 10 Dec 2014 thru 7 Apr 2015 Natures Place Veggie chips Net Wt. 6 oz Distributed By: DZA Brands, LLC, Salisbury NC 28147/Scarborough, ME 04074 With code dates: 15 Dec 2014 t
    Category
    Food
    Distribution
    8 states
  • SevereNHTSA·15V154000·2015-03-17

    Hyundai Translead Recalls 2014-2015 Trailers Due to Brake Drag Risk

    Hyundai Translead is recalling 3,412 model year 2014-2015 trailers because improperly seated brake diaphragms may cause drag, potentially leading to wheel end fires.

    Product
    HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD CONVERTER DOLLY TRAILER, VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·047-2015·2015-03-17

    Alewel's Country Meats Recalls Buffalo Jerky Due to Misbranding

    Alewel's Country Meats is recalling approximately 134 pounds of Buffalo Jerky because the product was produced using the wrong inspection legend.

    Product
    Alewel's Country Meats — Recall Notification Report 047-2015 (Buffalo Jerky)
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·15V151000·2015-03-16

    Spartan Tool Sewer Jetter Trailer Hitch Weld Failure Recall

    Spartan Tool is recalling 2013-2014 Sewer Jetters because trailer hitch welds may fail, causing the trailer to detach from the tow vehicle.

    Product
    SPARTAN TOOL — SPARTAN TOOL SEWER JETTER 740, SEWER JETTER 758, SEWER JETTER 738
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V152000·2015-03-16

    Ducati Recalls Multistrada 1200 Motorcycles Due to Throttle Cable Defect

    Ducati is recalling 2010-2014 Multistrada 1200 motorcycles because a moving throttle cable sleeve may prevent the throttle from closing fully, increasing crash risk.

    Product
    DUCATI — DUCATI MULTISTRADA 1200
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V150000·2015-03-16

    Altec Recalls 2014 Aerial Devices Due to Counterbalance Valve Defect

    Altec is recalling 2014 Aerial Devices because a counterbalance valve may crack, causing hydraulic leaks and unintended boom movement that increases injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide

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