The Recall Desk

Archive

April 2014 recalls

645 recalls were announced in April 2014.

What the numbers show

Critical
60
Severe
167
High
236
Moderate
162
Low
20

Of the 645 recalls this month scored against our rubric, 9% are Critical, 26% are Severe.

Which agencies issued them

1–100 of 645

  • CriticalFDA (Food)·F-1880-2014·2014-04-30

    Frontier and Simply Organic Black Peppercorns Recalled for Salmonella

    Frontier Natural Products Co-op is recalling various brands of organic whole black peppercorns because testing revealed the presence of Salmonella.

    Product
    1) Frontier Natural Products Co-op, Whole Black Peppercorns, Certified Organic, Piper nigrum. Net 11.3 Kg 25 LB. Packaged in corrugated cardboard boxes. Firm name on the label is Frontier in Norway, IA. UPC 0-89836-82603-9.; 2) Frontier Natural Products Co-op, Whole Black…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1251-2014·2014-04-30

    Shire Recalls VPRIV Vials Due to Presence of Particulate Matter

    Shire Human Genetic Therapies is recalling 8,359 vials of VPRIV (velaglucerase alfa) because they contain stainless steel and barium sulfate particles.

    Product
    VPRIV — VPRIV (VELAGLUCERASE ALFA)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1248-2014·2014-04-30

    Fossil Fuel Products Recalls RezzRX Capsules for Undeclared Ingredients

    Fossil Fuel Products, LLC is recalling RezzRX capsules because they contain undeclared hydroxylthiohomosildenafil and aminotadalafil.

    Product
    RezzRX capsules, Single Blister Pack and 20 count bottle, Distributed By: Fossil Fuel Products, LLC Atlanta, GA 30309
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1249-2014·2014-04-30

    JaDera Weight Loss Supplement Recalled for Undeclared Sibutramine

    Dolphin Intertrade Corporation is recalling JaDera weight loss capsules because they contain undeclared sibutramine, a drug removed from the U.S. market for safety reasons.

    Product
    JaDera, 100% Natural Weight Loss Supplement, capsules, 30 count bottle
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1878-2014·2014-04-30

    Creative Snacks Recalls Dried Apricots for Undeclared Sulfites

    Creative Snacks Co. is recalling dried apricots in cups and bags because they contain undeclared sulfites. The products were distributed in Massachusetts and New Jersey.

    Product
    Creative Snacks Co. Dried Apricots (10.5 oz Rigid Plastic Cup, and 7 oz Clear Plastic Bag), Distributed by: Creative Snacks, Co., Greensboro, NC 27409
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1879-2014·2014-04-30

    Sprouts Recalls Organic Whole Black Peppercorns Due to Salmonella Risk

    Sprouts Farmers Market is recalling Organic Whole Black Peppercorns because FDA tests found Salmonella in one lot and another lot poses a contamination risk.

    Product
    Sprouts Farmers Market Organic Whole Black Peppercorns, 2.12oz., UPC Code 8-74875-00425-4, Lot Numbers 3287 and 3246. Packaged in glass jars with plastic lid. Product labeling reads in part:"SPROUTS FARMERS MARKET organic Black Peppercorns ***NET WT 2.12 OZ…
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-1881-2014·2014-04-30

    Lisy Sweet Basil Recalled Due to Salmonella Contamination

    Lisy Corp. is recalling Sweet Basil Albahaca because an FDA sample tested positive for Salmonella. The product was distributed in four states.

    Product
    Lisy Sweet Basil Albahaca Net WT/Cont. Neto 6oz. (171g) Item 1132 www.lisycorp.com Packed on a clear plastic container with a UPC # 0 96786 30032 8
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Devices)·Z-1471-2014·2014-04-30

    Heartware HVAD Pump Implant Kit Recalled for Driveline Connector Separation

    HeartWare Inc is recalling HVAD Pump Implant Kits because the driveline connector housing may separate. This defect could affect patients using the device for heart failure.

    Product
    Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device) Catalog Numbers: 1100, 1101, 1102, 1103, 1104, and 1205. For use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V224000·2014-04-30

    GM Recalls 1.1 Million Vehicles for Transmission Shift Cable Fracture Risk

    General Motors is recalling 1,131,113 vehicles due to a transmission shift cable that may fracture, causing unintended movement or rollaway.

    Product
    CHEVROLET — CHEVROLET, PONTIAC, SATURN MALIBU MAXX, MALIBU, G6, AURA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E021000·2014-04-30

    UCI-FRAM Recalls Ignition Switches for GM Vehicles Due to Stalling Risk

    UCI-FRAM is recalling specific ignition switches used in GM vehicles because they may shift out of the run position, causing the engine to stall and disabling air bags.

    Product
    PONTIAC — PONTIAC, SATURN, CHEVROLET PURSUIT, ION, COBALT, SOLSTICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1481-2014·2014-04-30

    RaySearch Ray Station Software Recalled for Dose Miscalculations

    RaySearch Laboratories is recalling Ray Station software versions 2.0 through 4.0 due to dose miscalculations for support structures on CT images.

    Product
    RaySearch Ray Station Radiation Therapy Treatment Planning System, Stand-alone software. Versions 2.0, 2.5, 3.0, 3.5 and 4.0.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1492-2014·2014-04-30

    Ion Beam Applications Recalls Proteus 235 Proton Therapy System Software

    Ion Beam Applications is recalling Proteus 235 Proton Therapy System Legacy Software due to incorrect dose rate calculations for non-zero beam line options.

    Product
    Proteus 235 Proton Therapy System Legacy Software version 7.2.7 and higher, models 110, 112, 113, and 116. Proton therapy
    Category
    Medical Device
    Distribution
    4 states
  • SevereFDA (Food)·F-1882-2014·2014-04-30

    Natural Grocers Organic Black Peppercorns Recalled for Salmonella Risk

    Natural Grocers by Vitamin Cottage is recalling Organic Black Peppercorns due to potential Salmonella contamination.

    Product
    Natural Grocers by Vitamin Cottage, Pepper Black Whole Organic, about 0.30 lb, UPC 201046804762, packaged in plastic bags.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1480-2014·2014-04-30

    GE Healthcare Recalls MR Scanners Due to Gradient Coil Overheating Risk

    GE Healthcare is recalling 1,546 MRI scanners worldwide because gradient coil connections may loosen, causing overheating, smoke, and potential fire.

    Product
    GE Healthcare, Discovery MR450, Discovery MR750, Optima MR450w, Optima MR 450w GEM, Discovery MR750w, and Discovery MR750w GEM products. Magnetic Resonance Diagnostic Device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1883-2014·2014-04-30

    Jolly Time Microwave Popcorn Recalled for Metal Fragment Contamination

    American Pop Corn Co is recalling Jolly Time Microwave Popcorn due to potential contamination with stainless steel metal fragments.

    Product
    Jolly Time Microwave popcorn, Butter, 3/3-oz bags/carton. The cartons are packaged 12-cartons/case. Individual carton UPC 028190007876, on the 12-ct case - UPC 10028190007804 and 48-ct case UPC 128190487873 American Pop Corn Company, Sioux City, IA.
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Devices)·Z-1484-2014·2014-04-30

    Baxter Recalls Sigma Spectrum Volumetric Infusion Pumps Due to System Errors

    Baxter Healthcare is recalling Sigma Spectrum Volumetric Infusion Pumps due to repeated System Error 322 occurrences.

    Product
    SIGMA SPECTRUM Volumetric Infusion Pump with Master Drug Library Product Usage: Sigma Spectrum Volumetric Infusion Pumps with Master Drug Library are intended to be used for the controlled administration of intravenous fluids. These fluids may include pharmaceutical drugs…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1252-2014·2014-04-30

    Glycopyrrolate Injectable Recalled for Bacillus thuringiensis Contamination

    Brookfield Prescription Center Inc. is recalling one lot of Glycopyrrolate solution for injection due to Bacillus thuringiensis contamination.

    Product
    Glycopyrrolate (MDV) 0.2 MG/ML Injectable, 5 mL Vials, Sterile Serum Vials/Sterile Syringes, for use by a licensed professional only, not for resale, MD Custom Rx, 19035 W Capitol Dr Ste 105, Brookfield, WI 53045.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1261-2014·2014-04-30

    Hospira Recalls Potassium Chloride Vials Due to Particulate Matter

    Hospira is recalling 255,900 vials of Potassium Chloride for Injection due to the presence of red and black particulate matter identified as iron oxide.

    Product
    Potassium Chloride for Inj. Concentrate, USP, 40 mEq (2 mEq/mL), 20 mL Single-dose Fliptop Vial, For IV use, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·14166·2014-04-30

    White-Rodgers Recalls Home Heating and Cooling Thermostats Due to Fire Hazard

    White-Rodgers is recalling about 740,000 digital thermostats in the U.S. and 403,000 in Canada because leaking batteries can cause a fire. Consumers should check for a battery icon on the screen to see if their unit is affected.

    Product
    Home Heating and Cooling Thermostats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1503-2014·2014-04-30

    Philips Digital Diagnost Radiographic System Recall Due to Footboard Defect

    Philips is recalling 985 Digital Diagnost stationary radiographic systems because the footboard may not be securely held if the fix clamp is not correctly adjusted.

    Product
    Digital Diagnost, stationary radiographic system; Models: 712020/22/25/26/50/52/54/55/57/60/62/80/81/82/85
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V223000·2014-04-30

    GM Recalls 2014 Buick, Chevrolet, and GMC SUVs for Fuel Gauge Error

    General Motors is recalling 51,640 model year 2014 Buick Enclave, Chevrolet Traverse, and GMC Acadia vehicles because engine software may cause the fuel gauge to read inaccurately.

    Product
    CHEVROLET — CHEVROLET, GMC, BUICK TRAVERSE, ACADIA, ENCLAVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1493-2014·2014-04-30

    Stryker PenAdapt Electrosurgical Accessory Recalled for Sterile Barrier Breach

    Stryker is recalling 35,310 PenAdapt electrosurgical accessories due to packaging cuts that may breach the sterile barrier and the presence of aluminum shavings.

    Product
    Stryker PenAdapt"; Rx Only, Sterile. This device is an accessory to an electrosurgical unit (ESU). The PenAdapt is used to remove smoke, particles, and body and casual fluids from the point of surgical activity during surgical procedures that use ESU for cutting and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1509-2014·2014-04-30

    Teleflex Recalls Monodek Violet Synthetic Absorbable Surgical Sutures

    Teleflex Medical is recalling Monodek Violet Synthetic Absorbable Surgical Sutures because they do not meet minimum knot tensile strength requirements.

    Product
    Monodek Violet Synthetic Absorbable Surgical Sutures, MF 0 TC43/HR26 48
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1476-2014·2014-04-30

    BioMerieux Recalls FB Reagent Due to False Negative Test Results

    BioMerieux SA is recalling FB Reagent (REF 70562) and ZYM B reagent (REF 70493) because a visual defect and activity issue can cause false negative results in Rapid ID 32 and API biochemical tests.

    Product
    FB Reagent (REF 70562). FB reagent is an additional test used for revealing the results of some miniaturized biochemical test included in the API and Rapid ID 32 strips. The API and ID 32 strips product lines are a standardized system combining several biochemical tests…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1474-2014·2014-04-30

    Remel Recalls Oxoid Legionella Pneumo Groups 2-14 Test Kits

    Remel Inc is recalling two boxes of Oxoid Legionella Pneumo Groups 2-14 test kits because a reagent may produce false negative results.

    Product
    Oxoid Legionella Pneumo Groups 2-14, DR0802M, containing 50 tests per box. The box contains a variety of components, one of which is Oxoid L. pneumophila Group 2-14 Latex Reagent, DR0802. The responsible firm on the label is Oxoid Ltd., Basingstoke, Hants, England.
    Category
    Medical Device
    Distribution
    11 states
  • HighNHTSA·14V226000·2014-04-30

    Glaval Transit Bus Recall for Wheelchair Lift Cable Fire Risk

    Glaval is recalling 2007-2012 transit buses equipped with certain Ricon wheelchair lifts. An armored cable may not clear the lift, potentially causing a short circuit and fire.

    Product
    GLAVAL BUS — GLAVAL BUS, GLAVAL ENTOURAGE, CONCORDE, APOLLO, SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1495-2014·2014-04-30

    Philips MDC PACS and IntelliSpace PACS DCX Software Recall for Density Errors

    Philips is recalling MDC PACS and IntelliSpace PACS DCX software because it may display incorrect density measurements on Enhanced CT and MR examinations.

    Product
    Philips MDC PACS R2.X / IntelliSpace PACS DCX R3.1 software, software application that is used for receiving, managing, archiving, distributing and recording medical images onto portable digital media (including but not limited to Compact Disk and DVD). The MDC…
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Devices)·Z-1473-2014·2014-04-30

    Remel Recalls Oxoid Legionella Latex Test Due to False Negative Risk

    Remel Inc is recalling specific lots of Oxoid Legionella Latex Test kits because a reagent may produce false negative results.

    Product
    Oxoid Legionella Latex Test, DR0800M, containing 50 tests per box. The box contains a variety of components, one of which is Oxoid L. pneumophila Group 2-14 Latex Reagent, DR0802. The responsible firm on the label is Oxoid Ltd., Basingstoke, Hants, England.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Food)·F-1875-2014·2014-04-30

    CJ Bakery Recalls Cinnamon Manjoo Cookies for Undeclared Wheat

    CJ Bakery is recalling Cinnamon Cookie Manjoo products because they contain undeclared wheat, a major food allergen.

    Product
    Cinnamon Cookie Manjoo, 200g Net Weight. Packaged in clear plastic bag, 10 per bag. Product package labeled in part:"***Cinnamon Cookie (Manjoo)*** Net Wt. 200g, 7.1oz***Manufactured by: CJ Foodville USA, Inc. (323)480-9105***6834 E. Slauson Ave, Commerce, CA…
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1488-2014·2014-04-30

    GE Vivid E9 Ultrasound System Recalled for Probe Overheating Risk

    GE Healthcare is recalling Vivid E9 Ultrasound Systems because incorrect power settings for four specific probe types may cause them to overheat.

    Product
    GE Vivid E9 Ultrasound System, a general-purpose ultrasound system, specialized for use in cardiac imaging.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1877-2014·2014-04-30

    CJ Bakery Recalls Chocolate Madelines Due to Undeclared Wheat

    CJ Bakery is recalling chocolate madelines, madelines, and cinnamon manjoo because they contain undeclared wheat.

    Product
    Chocolate Madeline, 80g Net Weight. Packaged in clear plastic bag, 4 per bag. Product package labeled in part:"AUTHENIC BAKERY TOUS Les JOURS***Madeline*** Net Wt. 80g, 2.8oz ***Manufactured by: CJ Foodville USA, Inc. (323)480-9105***6834 E. Slauson Ave, Commerce, CA…
    Category
    Food
    Distribution
    6 states
  • HighCPSC·14165·2014-04-30

    Horizon Hobby Recalls Blade 700 X Helicopter Kits Due To Injury Hazard

    Horizon Hobby is recalling Blade 700 X Pro Series helicopter kits and spindle sets because a defective washer can cause rotor blades to detach, posing an injury risk.

    Product
    Radio-controlled helicopter kits and spindle sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1506-2014·2014-04-30

    Teleflex Recalls Sengstaken Tubes Due to Sterility Concerns

    Teleflex Medical is recalling Sengstaken and Sengstaken-Blakemore tubes because the sterility of the product cannot be guaranteed.

    Product
    Sengstaken Tube and Sengstaken-Blakemore Tube. Teleflex product codes 204800, 204802, and 204803, a gastrointestinal tube and accessories, consisting of flexible or semi-rigid tubing used for instilling fluids into, withdrawing fluids from, splinting, or suppressing bleeding…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1876-2014·2014-04-30

    CJ Bakery Recalls Madeline and Manjoo Products for Undeclared Wheat

    CJ Bakery is recalling specific baked goods due to undeclared wheat, posing a risk to individuals with wheat allergies or celiac disease.

    Product
    Madeline, 80g Net Weight. Packaged in clear plastic bag, 4 per bag. Product package labeled in part:"AUTHENIC BAKERY TOUS Les JOURS***Madeline*** Net Wt. 80g, 2.8oz ***Manufactured by: CJ Foodville USA, Inc. (323)480-9105***6834 E. Slauson Ave, Commerce, CA…
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1478-2014·2014-04-30

    BioMerieux Recalls ZYM B and FB Reagents Due to False Negative Results

    BioMerieux is recalling ZYM B and FB reagents because a visual defect and activity issue caused false negative results in Rapid ID 32 strips and API biochemical tests.

    Product
    API Listeria (REF 10300). ZYM B reagent is used and included inside of API NH (REF 10400) and API Listeria (10300). All of the APIs are standardized systems combining several biochemical tests that enable group or species identification of most microorganisms.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1885-2014·2014-04-30

    Jolly Time Microwave Popcorn Recalled for Metal Fragments

    American Pop Corn Co is recalling Jolly Time Microwave popcorn due to potential contamination with stainless steel metal fragments.

    Product
    Jolly Time Microwave popcorn, Homemade Classic Stovetop Flavor, 3/3-oz bags/carton. The cartons are packaged 12-cartons/case. Individual carton - UPC 028190007807, on the 12-ct case - UPC 10028190007804, 48-ct shipper UPC 128190487804 American Pop Corn Company, Sioux City, IA
    Category
    Food
    Distribution
    22 states
  • HighFDA (Food)·F-1884-2014·2014-04-30

    Jolly Time Microwave Popcorn Recalled for Metal Fragment Contamination

    American Pop Corn Co is recalling Jolly Time Extra Butter microwave popcorn due to potential contamination with stainless steel metal fragments.

    Product
    Jolly Time Microwave popcorn, Extra Butter, 3/3-oz bags/carton. The cartons are packaged 12-cartons/case. Individual carton - UPC 028190008477, on the 12 count case - UPC 10028190008474 and 48 ct shipper with UPC 128190488474 American Pop Corn Company, Sioux City, IA.
    Category
    Food
    Distribution
    22 states
  • ModerateFDA (Devices)·Z-1472-2014·2014-04-30

    Pega Medical Recalls Fassier-Duval IM Telescopic System Due to Labeling Error

    Pega Medical Inc. is recalling 48 units of the Fassier-Duval IM Telescopic System because the outer package label listed the incorrect device length.

    Product
    Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant. Catalogue number FD-040(L)-SS. -Duval IM Telescopic System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1500-2014·2014-04-30

    Meta Labs Recalls Nice-En-Smooth Berry Burst Lubricant for Unregistered Manufacturing

    Altasource LLC dba Meta Labs LLC is recalling Nice-En-Smooth Berry Burst lubricant because the firm is not registered as a drug manufacturer.

    Product
    Nice-En-Smooth Berry Burst, 4 oz., Manufactured by Meta Labs LLC, UPC 80604-8 Product Usage: Flavored lubricant water based, condom friendly jelly used to enhance or replace a womans natural lubrication.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1507-2014·2014-04-30

    Arrow Recalls Antimicrobial Central Venous Catheters Due to Labeling Error

    Arrow International is recalling 170 units of Arrowgard Blue Plus Antimicrobial Multi-lumen Central Venous Catheters because the lidstock incorrectly lists the catheter length as 16CM instead of 20CM.

    Product
    Arrowgard Blue Plus Antimicrobial Multi-lumen Central Venous Catheter, catalogue number AK-45854-CDC.
    Category
    Medical Device
    Distribution
    12 states
  • ModerateFDA (Drugs)·D-1242-2014·2014-04-30

    Nicorette Lozenges Recalled for Thickness and Potency Failures

    GlaxoSmithKline is recalling Nicorette 2 mg lozenges because they failed specifications for thickness, softness, and potency.

    Product
    Nicotine polacrilex lozenge, 2 mg, Mint Flavor, 81 count cartons and 189 count cartons. OTC. Labeled Nicorette, Distributed By: GlaxoSmithKline Consumer Healthcare, L.P., Moon Township, PA 15108. Made in Switzerland. 81 Count NDC: 0135-0510-05, 189 Count NDC: 0135-0510-03.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1253-2014·2014-04-30

    Pfizer Recalls Tikosyn Capsules Due to Foreign Object Contamination

    Pfizer is recalling Tikosyn (dofetilide) 500 mcg capsules because a single 250 mcg capsule was found in one bottle. The recall covers 23,064 bottles distributed nationwide.

    Product
    Tikosyn¿ (dofetilide) 500 mcg (0.5mg) capsules, 60-count bottle, Rx only Pfizer Labs, Division of Pfizer Inc. NY, NY 10017, NDC 00069-5820-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1254-2014·2014-04-30

    P&L Developments Recalls Subpotent Day Time Cold & Flu OTC Drug

    P&L Developments, LLC is recalling 2,500,510 bottles of Day Time Cold & Flu because the phenylephrine component is subpotent.

    Product
    Day Time Cold & Flu, Multi-Symptom, Non-Drowsy, Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 4, 6, 8, 10, and 12 oz Bottles, OTC Only. Labeled A) Aaron Health, 10 FL OZ, Manufactured by Aaron Industries, P.O. Box 801, Lynwood, CA 90262, UPC: 7 15256 73510 0; B) Aaron…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1489-2014·2014-04-30

    Ev3 Recalls EverCross PTA Dilatation Catheters Due to Labeling Error

    Ev3 is recalling two lots of EverCross PTA Dilatation Catheters because of a discrepancy in the balloon and delivery catheter lengths printed on the product labeling.

    Product
    ev3 EverCross 0.035" OTW PTA Dilatation Catheter, 6mm x 120mm x 135cm, REF: AB35W06120135. and ev3 EverCross 0.035" OTW PTA Dilatation Catheter, 6mm x 40mm x, 80cm REF: AB35W06040080. Peripheral Dilatation Catheter
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1479-2014·2014-04-30

    Hospira Recalls HemoSet IV Sets Due to Incorrect Lower Lid Component

    Hospira is recalling 3,893 HemoSet IV sets because an incorrect lower lid was used during manufacturing, which changes the drop rate from 15 to 10 drops per mL.

    Product
    LifeShield LATEX-FREE HemoSet 100 mL Burette I.V. PlumSet, Nonvented, 105 inch with Prepierced Reseals, OPTION-LOK and Inline Dual Channel Cassette. For administration of blood and blood bags for use with Plum Series Infusers.
    Category
    Medical Device
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-1486-2014·2014-04-30

    Merit Medical Recalls Hydrophilic Guide Wires Due to Labeling Discrepancy

    Merit Medical Systems is voluntarily recalling specific lots of Laureate Hydrophilic Guide Wires due to a discrepancy between carton and unit labeling.

    Product
    Merit Laureate 0.035" (0.89mm) Hydrophilic Guide Wire, Angled Tip, Standard Shaft, Catalog No. LWSTDA35260EX, 260 cm (102").
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1243-2014·2014-04-30

    GlaxoSmithKline Recalls Nicorette Lozenges Due to Quality Failures

    GlaxoSmithKline is recalling Nicorette 4 mg lozenges because they failed specifications for thickness, softness, and potency.

    Product
    Nicotine polacrilex lozenge, 4 mg, Mint Flavor, 81 Lozenge and 189 Lozenge Vials. OTC. Labeled Nicorette, Distributed By: GlaxoSmithKline Consumer Healthcare, L.P., Moon Township, PA 15108. Made in Switzerland. 81 Count NDC: 0135-0511-05, 189 Count NDC: 0135-0511-03.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1497-2014·2014-04-30

    Teleflex Medical Recalls Non-absorbable Steel Sutures for Diameter Defects

    Teleflex Medical is recalling specific lots of non-absorbable steel sutures because they did not meet minimum diameter requirements.

    Product
    Monofilament and Multifilament Non-absorbable Steel Suture; Product Codes: 0520197-2, 29-727, 29-7270M4, 29-7281M4, E29-5553M4, E29-7270M4, E29-7272M4, E29-727A, EP4013P, EP4110N, X-2235, X29-7271M2, X-5667M8 and X-6730M5.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1496-2014·2014-04-30

    Zimmer Trabecular Metal Hip Implant Shell Recalled for Missing Locking Ring

    Zimmer, Inc. is recalling 17 units of Trabecular Metal Modular Acetabular System shells because the locking ring was missing.

    Product
    TRABECULAR METAL MODULAR ACETABULAR SYSTEM, Shell with Cluster Holes, Porous 60mm. Catalog number 00-6202-060-22; Hip implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1485-2014·2014-04-30

    Merit Medical Recalls Mixed Hydrophilic Guide Wire Lots

    Merit Medical Systems is recalling 173 units of Laureate Hydrophilic Guide Wire due to a labeling discrepancy where the product was mixed with a different lot.

    Product
    Merit Laureate Hydrophilic Guide Wire, Catalog No. LWSTFS35260EX, Straight Tip Stiff Shaft, 0.035" (0.89mm), 260 cm (102").
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1499-2014·2014-04-30

    Meta Labs Recalls Mega-Gen Personal Lubricant Due to Unregistered Manufacturer

    Altasource LLC is recalling Mega-Gen His and Hers Personal Lubricant because the firm is not registered as a drug manufacturer.

    Product
    Mega-Gen His Personal Lubricant, 8 fl. oz., Meta Labs, UPC Code 80708-3; Mega-Gen Hers Personal Lubricant, 8 fl. oz., Meta Labs, UPC Code 80808-0 Product Usage: A topical gel that increases sexual excitement and pleasure.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1475-2014·2014-04-30

    BioMerieux Recalls ZYM B Reagent Due to Visual Defect and Activity Issue

    BioMerieux SA is recalling ZYM B Reagent (REF 70493) because a visual defect and activity issue can cause false negative results in microbiological tests.

    Product
    ZYM B Reagent (REF 70493). The ZYM B reagent is an additional test used to reveal the results of some miniaturized biochemical test included in the API strips. The API product line is a standardized system combining several biochemical tests, which enables group or species…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1504-2014·2014-04-30

    Siemens ACUSON X700 Ultrasound Systems Recalled for Data Error

    Siemens is recalling 490 ACUSON X700 ultrasound systems because previous patient data may replace current patient dates in reports.

    Product
    Siemens ACUSON X700 Ultrasound Systems with software version 1.0.00, 1.0.01, 1.0.02, 1.1.00 and 1.1.02. ultrasound imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1491-2014·2014-04-30

    Abbott Molecular Recalls CEP 8 Probe Kits Containing Incorrect Probe

    Abbott Molecular is recalling 20 kits of CEP 8 SG ASR Probe that contained the wrong probe. The kits contained Vysis CEP 4 probe instead of the expected CEP 8 probe.

    Product
    The CEP 8 SpectrumGreen (SG) ASR Probe Kit, 20ul (list 06J37-018) is an Analyte Specific Reagent (ASR) containing a single vial of CEP 8 spectrum green probe and a Certificate of Analysis (COA). Chromosome enumeration probes (CEP) are chromosome-specific FISH probes that…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1240-2014·2014-04-30

    GlaxoSmithKline Recalls Nicorette Lozenges Due to Failed Specifications

    GlaxoSmithKline is recalling specific lots of Nicorette 4 mg lozenges because they failed quality specifications, including being overly thick, soft, and sub or superpotent.

    Product
    NICORETTE — NICORETTE (NICOTINE POLACRILEX)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1241-2014·2014-04-30

    GlaxoSmithKline Recalls Nicorette Lozenges Due to Failed Specifications

    GlaxoSmithKline is recalling specific lots of Nicorette 2 mg lozenges because they failed quality specifications, including being overly thick, soft, and sub or superpotent.

    Product
    NICORETTE — NICORETTE (NICOTINE POLACRILEX)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1246-2014·2014-04-30

    GlaxoSmithKline Recalls Nicorette Lozenges Due to Failed Specifications

    GlaxoSmithKline is recalling specific lots of Nicorette lozenges because they failed quality specifications, including being overly thick, soft, and sub or superpotent.

    Product
    NICORETTE — NICORETTE (NICOTINE POLACRILEX)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1501-2014·2014-04-30

    Meta Labs Recalls Hot Ice Topical Gel Due to Unregistered Manufacturer

    Altasource LLC dba Meta Labs LLC is recalling 155 units of Hot Ice topical gel because the firm is not registered as a drug manufacturer.

    Product
    Hot Ice, 1 fl. oz., Meta Labs LLC, UPC 80705-2 Product Usage: A topical gel that increases men and womens secual excitement and pleasure.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1498-2014·2014-04-30

    FDA Recalls Amo-O Herbal Stimulator Gel for Unregistered Manufacturer

    Altasource LLC is recalling 70 units of Amo-O Herbal Stimulator gel because the firm is not registered as a drug manufacturer.

    Product
    Amo-O Herbal Stimulator, 2 fl. oz. Manufactured by Meta Labs, Alpharetta, GA 30076, UPC Code 80702-1 Product Usage: The product is a nonprescription, topical gel that is used to enhance libido and stimulate orgasmic pleasure.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1477-2014·2014-04-30

    BioMerieux Recalls ZYM B and FB Reagents Due to False Negative Results

    BioMerieux is recalling ZYM B and FB reagents because a visual defect and activity issue can cause false negative results in Rapid ID 32 strips and API biochemical tests.

    Product
    API NIH (REF 10400). ZYM B reagent is used and included inside of API NH (REF 10400) and API Listeria (10300). All of the API's are standardized systems combining several biochemical tests that enable group or species identification of most microorganisms.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1239-2014·2014-04-30

    GlaxoSmithKline Recalls Nicotine Lozenges Due to Failed Specifications

    GlaxoSmithKline is recalling Nicorette and store-brand nicotine lozenges because they failed quality specifications, including being overly thick, soft, and sub or superpotent.

    Product
    Nicotine polacrilex lozenge, 4 mg, Cherry Flavor, 72 count cartons, 81 count cartons, and 108 count cartons. OTC. Labeled a. Nicorette, Distributed By: GlaxoSmithKline Consumer Healthcare, L.P., Moon Township, PA 15108. Made in Switzerland. 72 Count NDC: 0135-0513-01, 81 Count…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1508-2014·2014-04-30

    Branan Medical ToxCup Drug Screen Cups Recalled for Labeling Errors

    Branan Medical is recalling ToxCup Drug Screen Cups because the lid labels may contain incorrect result interpretation graphics.

    Product
    ToxCup Drug Screen Cup, Catalogue Numbers: HT15, HT15A, PT11, PT11A, PT15A, PT23A, a screening device for the detection of drugs and drug metabolites in human urine. For in vitro diagnostic use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1502-2014·2014-04-30

    Varian On-Board Imager Elbow Motor Shaft Recall

    Varian Medical Systems is recalling On-Board Imager devices with Type 01 elbow motors due to a shaft failure caused by belt over-tensioning.

    Product
    On-Board Imager - Exact Arm Elbow Motor Shaft (kVD, kVS, and MV) with ''Type 01" elbow motors. Product Usage: The On-Board Imager device is an x-ray device used for evaluation of correct patient position in relation to isocenter and verification of treatment fields in…
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1487-2014·2014-04-30

    Boston Scientific Recalls iLab Ultrasound Systems Due to Measurement Error

    Boston Scientific is recalling 9 iLab Ultrasound Imaging Systems because a software update may cause the Longview distance measurement to display double the actual value.

    Product
    iLab Ultrasound Imaging System; iLab 3.0 (Polaris 1.0) software. Used for ultrasound examinations of intravascular pathology.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1238-2014·2014-04-30

    GlaxoSmithKline Recalls Nicotine Lozenges Due to Failed Specifications

    GlaxoSmithKline is recalling Nicorette and store-brand nicotine lozenges because they failed specifications for thickness, softness, and potency.

    Product
    Nicotine polacrilex lozenge, 2 mg, Cherry Flavor, 72 count vials, 81 count vials, and 108 count vials. OTC. Labeled a. Nicorette, Distributed By: GlaxoSmithKline Consumer Healthcare, L.P., Moon Township, PA 15108. Made in Switzerland. 72 Count NDC: 0135-0512-01, 81 Count NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1490-2014·2014-04-30

    Ortho-Clinical VITROS Chemistry Calibration Data Module Recalled for Calibration Failure

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products CDM PROM No. 0168 because it lacks calibration parameters for DT CRSC slides, preventing system calibration.

    Product
    VITROS Chemistry Products CDM PROM (Calibration Data Module) No. 0168, Catalog Number/REF 199 9077, used in conjunction with: VITROS Chemistry Products CRSC DT Slides, Generation (GEN) 82, REF 6802721, and VITROS DT Calibrator Kit, Product Code 1957924, and tested on the VITROS…
    Category
    Medical Device
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-1494-2014·2014-04-30

    Arrow Pressure Injectable PICC Catheter Recall Due to Incorrect Length

    Arrow International Inc. is recalling 789 units of Arrow Pressure Injectable PICC catheters because they contain a 40cm catheter instead of the required 50cm catheter.

    Product
    Arrow Pressure Injectable PICC Powered by Arrow VPS Stylet Catalogue number CDC-35052-VPS, peripherally inserted central catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1505-2014·2014-04-30

    Siemens Multix Fusion Radiographic System Recall for Loose Hose Holder

    Siemens is recalling 12 Multix Fusion radiographic systems because a corrugated hose holder may become loose. The issue requires verification and securing of the holder.

    Product
    MULTIX FUSION. The Multix Fusion system is a radiographic system used in hospitals, clinics, and medical practices. Multix Fusion enables radiographic exposures of the whole body including: skull, chest, abdomen, and extremities and may be used on pediatric, adult and…
    Category
    Medical Device
    Distribution
    8 states
  • LowFDA (Drugs)·D-1255-2014·2014-04-30

    Upsher Smith Recalls Oxandrolone Tablets Due to Missing Primary Labels

    Upsher Smith Laboratories is recalling 36 bottles of Oxandrolone Tablets, USP, 10 mg, because they were packaged without primary labels.

    Product
    Oxandrolone Tablets, USP, 10 mg, Rx Only, C-III, 60-count bottle, Manufactured for: Upsher-Smith Labs, Minneapolis, MN 55447, by: Pharmaceutics International, Inc., Hunt Valley, MD 21031, NDC 0245-0272-06
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1245-2014·2014-04-30

    GlaxoSmithKline Recalls Nicorette Lozenges Due to Failed Specifications

    GlaxoSmithKline is recalling specific lots of Nicorette Lozenges Mini because they failed quality specifications, including being overly thick, soft, and sub or superpotent.

    Product
    NICORETTE — NICORETTE (NICOTINE POLACRILEX)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1247-2014·2014-04-30

    GlaxoSmithKline Recalls Nicorette Lozenge and NicoDerm CQ Combination Pack

    GlaxoSmithKline is recalling a specific lot of Nicorette Lozenge and NicoDerm CQ combination packs because the lozenges failed quality specifications.

    Product
    Nicorette Lozenge and NicoDerm CQ, nicotine polacrilex system. 189 2mg Mint Flavored Lozenges + 21 31 mg Patches. OTC Only. GlaxoSmithKlein, 1000 GSK Drive, Moon Township, PA 15108. UPC: 0-03-0766-1480-30-2.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1244-2014·2014-04-30

    GlaxoSmithKline Recalls Nicorette and Nicoderm CQ Products for Quality Failures

    GlaxoSmithKline is recalling specific lots of Nicorette and Nicoderm CQ products because the lozenges failed quality specifications, including being overly thick, soft, and having incorrect potency.

    Product
    Nicorette Lozenge, Nicoderm CQ, and Nicorette Gum nicotine polacrilex combination. Contains 30 Pieces/ Pallet. OTC only. GlaxoSmithKlein, 1000 GSK Drive, Moon Township, PA 15108. UPC: 0-03-0766-1442-81-2.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalCPSC·14161·2014-04-29

    IKEA Recalls Children's Wall-Mounted Lamps Due to Strangulation Hazard

    IKEA is recalling approximately 3.5 million children's wall-mounted lamps in the U.S. because the electrical cords pose a strangulation risk to infants.

    Product
    Children's wall-mounted lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V242000·2014-04-29

    Freightliner Recalls 2013 Cascadia Trucks Due to Missing Axle Snap Rings

    Daimler Trucks North America is recalling 2013 Freightliner Cascadia trucks because a missing axle snap ring could cause rear wheels to separate, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·14162·2014-04-29

    DGL Group Recalls Vibe USB Mobile Power Bars Due to Fire Hazard

    DGL Group is recalling Vibe USB Mobile Power Bars sold at Five Below because they can overheat and cause fires. No injuries have been reported, but minor property damage has occurred.

    Product
    Vibe USB Mobile Power Bar
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E019000·2014-04-29

    Meritor Recalls Wheel Ends Due to Missing Locking Snap Ring

    Meritor is recalling specific drive axle wheel ends manufactured between August and December 2012 because a missing locking snap ring could cause rear wheels to separate from the vehicle.

    Product
    FCCC — FCCC MC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·14164·2014-04-29

    GE Brand Dehumidifiers Recalled by Midea Due to Fire Hazard

    Midea is recalling GE brand dehumidifiers sold at Walmart because a compressor component can short circuit, posing a fire hazard.

    Product
    GE Brand Dehumidifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14731·2014-04-29

    Kawasaki Recalls 2014 Off-Road Motorcycles Due to Crash Hazard

    Kawasaki is recalling about 611 model year 2014 KLX110 and KLX110L off-road motorcycles because camshaft sprocket bolts can loosen, causing the engine to lock and creating a crash hazard.

    Product
    Off-Road Motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V218000·2014-04-28

    Nissan Recalls 2014 Rogue Vehicles Due to Steering Column Bolt Defect

    Nissan is recalling 2014 Rogue vehicles because an incorrect bolt may have been used in the steering column, which could loosen and cause a loss of vehicle control.

    Product
    NISSAN — NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V222000·2014-04-25

    Gillig Recalls 2012-2014 Low Floor Buses Due to Electrical Wiring Defect

    Gillig is recalling 2,274 Low Floor transit buses from 2012-2014 because electrical harnesses may corrode, potentially causing loss of engine, transmission, and ABS control.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V213000·2014-04-25

    GM Recalls 2015 Silverado HD and Sierra HD Diesel Trucks

    General Motors is recalling 2015 Chevrolet Silverado HD and GMC Sierra HD diesel trucks because improperly torqued fuel pipe connections may cause a fuel leak and potential fire.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO HD, SIERRA HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14T003000·2014-04-25

    Lionshead Recalls Vail Sport ST LH 99 Trailer Tires for Missing Markings

    Lionshead Specialty Tire & Wheel LLC is recalling approximately 4,000 Vail Sport ST LH 99 trailer tires manufactured between April 2012 and February 2013 because they may lack required load range markings.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·026-2014·2014-04-25

    Knockum Hill Bar-B-Que Recalls Pork Products Due To Undeclared Soy Allergen

    Knockum Hill Bar-B-Que is recalling approximately 350 pounds of hickory smoked barbecue pork products because they contain an undeclared soy allergen.

    Product
    Knockum Hill Bar-B-Que — Kentucky Firm Recalls Pork Products Due To Misbranding And Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·025-2014·2014-04-24

    Cobblestone Farms Pork Baby Back Ribs Recalled for Missing Border Inspection

    Skilcor Food Products is recalling 36 pounds of Cobblestone Farms pork baby back ribs because they were not presented for USDA inspection at the U.S. border.

    Product
    Ontario Firm Recalls Baby Back Ribs Produced Without Import Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·14V210000·2014-04-24

    Westward Recalls 2013 Go-4 Vehicles Due to Brake Pad Ejection Risk

    Westward is recalling 80 model year 2013 Go-4 vehicles because worn front brake pads may be ejected, reducing braking performance and increasing crash risk.

    Product
    WESTWARD — WESTWARD GO-4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V221000·2014-04-24

    Utility Recalls 2015 Refrigerated Vans Due to Axle Bearing Failure Risk

    Utility Trailer Manufacturing Company is recalling 2015 VS1RA, VS2RA, and VS3RA refrigerated vans because over-tightened axle nuts may cause bearing failure and loss of vehicle control.

    Product
    UTILITY — UTILITY VS1RA, VS3RA, VS2RA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·14159·2014-04-24

    Felt Triathlon Bicycles Recalled Due to Fork Steer Tube Breakage Risk

    Felt Bicycles is recalling 2008 and 2010 triathlon models because the steer tube can break, causing loss of control and injury.

    Product
    2008 Felt S22 and S32 Triathlon Bicycles and 2010 Felt S32, B12, B14 and B16 Triathlon Bicycles.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14157·2014-04-24

    Sugarfly Girls' Peacoats Recalled for Waist Drawstring Entanglement Hazard

    Runway Global is recalling Sugarfly girls' peacoats because the waist drawstring poses an entanglement hazard. Consumers should detach the tie or return the coat for a refund.

    Product
    Girls' Sugarfly Peacoats with a waist drawstring
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14158·2014-04-24

    Ariens Recalls Snow Throwers and Power Brushes Due to Amputation Hazards

    Ariens is recalling about 5,700 snow throwers and power brushes because a drive pulley can crack, causing the machine to keep running after the clutch is disengaged.

    Product
    Ariens and Sno-Tek Snow Throwers, Ariens and Gravely All-Season Power Brushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1840-2014·2014-04-23

    Parkers Farm Green Onion Cheeseball Base Cold Pack Cheese Recalled for Listeria Risk

    Parkers Farm Inc. is recalling Green Onion Cheeseball Base Cold Pack Cheese due to potential Listeria monocytogenes contamination.

    Product
    Green Onion Cheeseball Base Cold Pack Cheese sold under the following sizes and brands: Parkers Farm or Parkers label in 5 lb. (13331) pail with snap on lid;
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1869-2014·2014-04-23

    Parkers Farm Peanut Butter Recalled for Listeria Contamination Risk

    Parkers Farm Inc. is recalling specific sizes of Crunchy Peanut Butter due to potential Listeria monocytogenes contamination.

    Product
    Peanut Butter sold under the following sizes, brands, and textures: 1. 16 oz tubs with snap on lid (12 tubs in box) Parkers Farm CRUNCHY (55104), 2. 34 oz. tubs with snap on lid (6 tubs in box) Parkers Farm CRUNCHY (55304)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1237-2014·2014-04-23

    FDA Recalls Virilis Pro Dietary Supplement for Unapproved Drug Ingredients

    Haute Health is recalling Virilis Pro dietary supplements because they may contain unapproved active ingredients found in FDA-approved erectile dysfunction drugs.

    Product
    Virilis Pro, 450mg/capsule, Packaged in a 1 and 2 capsule blister packs and 10 capsule bottles, Manufactured for Haute Health Williamstown, NJ 08094 website: http://www.virilispro.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1849-2014·2014-04-23

    Parkers Farm Jalapeno Nacho Dip Recalled for Listeria Risk

    Parkers Farm Inc is recalling Jalapeno Nacho Dip due to potential Listeria monocytogenes contamination. Consumers should check sell-by dates and discard affected products.

    Product
    Jalapeno Nacho Dip sold under the following sizes and brands: Parkers Farm or Parkers label in 12 ounce (20200) cups with snap on lids.
    Category
    Food
    Distribution
    Distributed nationwide

Looking for a different month? Back to 2014.