The Recall Desk

Archive

December 2013 recalls

1,402 recalls were announced in December 2013.

What the numbers show

Critical
354
Severe
585
High
206
Moderate
225
Low
32

Of the 1,402 recalls this month scored against our rubric, 25% are Critical, 42% are Severe.

Which agencies issued them

601–700 of 1402

  • HighFDA (Devices)·Z-0477-2014·2013-12-18

    Zimmer Trabecular Metal Total Ankle Tibial Base Component Recall

    Zimmer, Inc. is recalling specific sizes of the Trabecular Metal Total Ankle Tibial Base Component due to potential elevated levels of manufacturing residue.

    Product
    Zimmer Trabecular Metal Total Ankle Tibial Base Component Sizes 1-6 Total ankle arthroplasty is intended to provide a patient with limited mobility by restoring alignment, reducing pain and preserving the flexion/extension movement within the ankle joint.The Zimmer Trabecular
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0457-2014·2013-12-18

    Hospira Recalls Receptal Canisters Due to Suction Failure

    Hospira is recalling 1L Receptal Canisters because the canister and liner may not seat properly, preventing the creation of necessary suction.

    Product
    Product is labeled in part: LIST NO. 43449; RECEPTAL CANISTER; DO NOT FILL 900 ABOVE THIS LINE; Product of China; Hospira, Inc.,; Lake Forest, IL 60045 USA. Used to isolate suction waste during surgeries, or to clear patient airways, throat or wounds to allow treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0463-2014·2013-12-18

    Zimmer NexGen Knee Instruments Recalled Due to Potential Surgical Delay

    Zimmer, Inc. is recalling five NexGen Micro knee instruments because they may be used incorrectly, causing surgical delays.

    Product
    NexGen Complete Knee Solution CR Articular Surface Provisional-Striped Green 9mm Height Nonsterile Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders, post-traumatic lo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-340-2014·2013-12-18

    Novartis Recalls Tekturna HCT Physician Samples Due to Chemical Contamination

    Novartis is recalling Tekturna HCT physician sample bottles due to contamination with Darocur 1173, a photo curing agent used in ink.

    Product
    Tekturna HCT (aliskiren and hydrochlorothiazide) Tablets 300/25 mg, 7 tablets per bottle, Physician Sample-Not For Sale, Rx only, Manufactured by: Novartis Pharma Productions GmbH Wehr, Germany. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936, NDC
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0461-2014·2013-12-18

    Zimmer NexGen Knee Implant Components Recalled for Surgical Delay Risk

    Zimmer, Inc. is recalling 638 NexGen Complete Knee Solution provisional articular surface devices. The recall is an expansion of a previous action to prevent inadvertent use of associated instruments.

    Product
    NexGen Complete Knee Solution CR Articular Surface Provisional-Purple 9mm Height Nonsterile Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders, post-traumatic loss of
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0460-2014·2013-12-18

    Zimmer NexGen Porous Patella Drill Guide Recall Expansion

    Zimmer, Inc. is expanding a recall of NexGen Porous Patella Drill Guides to prevent inadvertent use during surgery, which could cause delays.

    Product
    NexGen Complete Knee Solution Porous Patella Drill Guide-29mm dia./10mm thickness Non sterile, Rx Only Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders, post-traumat
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0470-2014·2013-12-18

    Beckman Coulter Recalls LH 750 Hematology Analyzers Due to Optical Degradation

    Beckman Coulter is recalling LH 750 Hematology Analyzers because optical degradation may delay reporting results for specific blood cell counts.

    Product
    Coulter LH 750 Hematology Analyzer, Part No. 6605632, A85570 Product Usage: The Coulter LH 750 Hematology Analyzer is a quantitative, automated hematology analyzer and leukocyte differential counter For In Vitro Diagnostic Use in clinical laboratories. The Coulter¿ LH 750 He
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0479-2014·2013-12-18

    Aesculap GNI161 Bipolar Foot Control Recalled for Energy Failure

    Aesculap, Inc. is recalling 85 GNI161 Bipolar Foot Controls because the bipolar energy did not stop after the foot control was released.

    Product
    Aesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar Coagulator is intended for use in surgery to generate electrical power for bipolar instruments. Bipolar coagulators are used in neurosurgery, ENT surgery, urology, laparoscopy, and plastic surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0456-2014·2013-12-18

    IBA COMPASS Software Recall for Erroneous Dose Statistics

    IBA Dosimetry GmbH is recalling COMPASS SW Version 3.0 due to a software defect that causes erroneous dose statistics and DVHs.

    Product
    iba COMPASS SW Version 3.0, Catalog Number CS10-100 (medical linear accelerator) radiological
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Devices)·Z-0484-2014·2013-12-18

    Trumpf Medical Systems Recalls Helion S and H300 Exam Lights

    Trumpf Medical Systems is recalling 287 Helion S and H300 exam lights because a plastic joint may fail due to fatigue after seven years of use.

    Product
    Helion S Exam Light or H300 The device is intended to locally illuminate an examination area of the patient's body with high intensity light in a clinic or doctor's practice.
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0466-2014·2013-12-18

    Maquet Vasoview Hemopro Endoscopic Vessel Harvesting System Recalled for Overheating

    Maquet Cardiovascular is recalling 12,259 units of the Vasoview Hemopro Endoscopic Vessel Harvesting System due to complaints that the device self-activates or overheats.

    Product
    Vasoview Hemopro Endoscopic Vessel Harvesting System Maquet Cardiovascular LLC 45 Barbour Pond Drive Wayne, NJ 07470 Indicated for use in minimally invasive surgery allowing access for vessel harvesting and is primarily indicated for patients undergoing endoscopic surgery for
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0468-2014·2013-12-18

    Arrow Transradial Artery Access Products Recalled for Occluded Needles

    Arrow International Inc is recalling Transradial Artery Access products because introducer needles may be occluded, posing a risk of delayed treatment or adverse events.

    Product
    Arrow Transradial Artery Access products Arrow Transradial Artery Access products are used for percutaneous introduction of devices into the radial artery for diagnostic and therapeutic purposes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0480-2014·2013-12-18

    Zimmer Recalls NexGen Knee Components Due to Stem Locking Failure

    Zimmer, Inc. is recalling 128 NexGen Complete Knee Solutions Stemmed Tibial Components because the stem may not lock into the tibia.

    Product
    NexGen¿ Complete Knee Solutions Stemmed Tibial Component Precoat NexGen Tibial Baseplates are part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis. The device is indicated for patients with severe knee pain and disability due to: Rheumatoid arthr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0817-2014·2013-12-18

    Sugar-Free Carrot Cake Recalled for Missing Phenylketonuria Warning

    Cakes & More Delight's is recalling sugar-free carrot cakes because they contain aspartame but lack the required phenylketonuria warning.

    Product
    Sugar free cake: Carrot flavor, Package size: 4 oz, 12 oz.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0482-2014·2013-12-18

    Accumetrics Recalls VerifyNow IIb/IIIa Test Kits Due to Incorrect Instructions

    Accumetrics is recalling VerifyNow IIb/IIIa Test Kits because they contain incorrect instructions regarding the time limit for performing the test after sample collection.

    Product
    VerifyNow IIb/IIIa Test, 10-Test Kit, Catalog No. 85310, 10 tests/box; 690 total tests. The VerifyNow IIb/IlIa Test is a semi-quantitative, whole blood platelet function test used to measure glycoprotein (GP) lIb/IlIa receptor blockade in patients treated with abciximab or
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-338-2014·2013-12-18

    Novartis Recalls Tekturna Tablets Due to Chemical Contamination

    Novartis is recalling Tekturna physician sample bottles contaminated with Darocur 1173, a photocuring agent found in ink.

    Product
    Tekturna (aliskiren) Tablets 300 mg, 7 tablets per bottle, Physician Sample-Not For Sale, Rx only. Manufactured by: Novartis Pharma Produktions GmbH Wehr, Germany. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936, NDC # 0078-9486-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-331-2014·2013-12-18

    Novartis Recalls Multiple Prescription Medications Due to Chemical Contamination

    Novartis is recalling physician sample bottles of several prescription medications due to contamination with a photocuring agent found in ink.

    Product
    Exforge HCT (amlodipine, valsartan, hydrochlorothiazide) 5/160/12.5 mg, Rx only, 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured by: Novartis Pharma Stein AG Stein, Switzerland. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936, ND
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0471-2014·2013-12-18

    Beckman Coulter Recalls LH 750 and LH 780 Hematology Systems

    Beckman Coulter is recalling LH 750 and LH 780 Hematology Systems because optical degradation may delay reporting results for specific blood cell counts.

    Product
    Coulter LH 780 Hematology Analyzer, Part No. 723585, A90728 Product Usage: Coulter LH 780 Hematology Analyzer is a is a quantitative, automated hematology analyzer and leukocyte differential counter For In Vitro Diagnostic Use in clinical laboratories. The Coulter¿ LH 780 He
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0467-2014·2013-12-18

    Stryker Recalls Accolade II Hip Stems Due to Packaging Error

    Stryker is recalling 20 Accolade II Hip Stems because a Size #3 was found packaged with a Size #5. The error poses a risk of incorrect implant selection.

    Product
    1) Accolade II 127 Neck Angle Hip Stem, Size # 3 2) Accolade II 127 Neck Angle Hip Stem, Size #5 Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430 USA Telephone # +1 201-831-5000 Stryker France ZAC Satolas Green Pusignan Av de Satolas Green 69881 MEYZI
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-329-2014·2013-12-18

    Novartis Recalls Exforge Physician Samples Due to Chemical Contamination

    Novartis is recalling Exforge physician sample bottles due to contamination with Darocur 1173, a photocuring agent used in ink.

    Product
    Exforge (amlodipine and valsartan Tablets) 5/320 mg, Rx only 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured by: Novartis Pharma Stein AG Stein, Switzerland. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936 - NDC # 0078-9490-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0473-2014·2013-12-18

    Synthes TomoFix Osteotomy System Recalled for Surgical Technique Guide Labeling Error

    Synthes USA HQ, Inc. is recalling the TomoFix Osteotomy System due to a labeling error in the Surgical Technique Guide that may cause surgical delays.

    Product
    Synthes TomoFix Plates The Synthes J5606-C TomoFix Osteotomy System is used for open and closed wedge osteotomies of the medial proximal tibia, lateral proximal tibia, medial and lateral distal femur, treatment of bone and joint deformities, fractures, and malalignment caused
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-346-2014·2013-12-18

    Lupin Recalls Ethambutol Hydrochloride Tablets Due to Impurity

    Lupin Pharmaceuticals is recalling 4,896 bottles of Ethambutol Hydrochloride 400 mg tablets because of an out-of-specification impurity result.

    Product
    ETHAMBUTOL HYDROCHLORIDE — ETHAMBUTOL HYDROCHLORIDE (ETHAMBUTOL HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-339-2014·2013-12-18

    Novartis Recalls Tekturna HCT Physician Samples Due to Chemical Contamination

    Novartis is recalling physician sample bottles of Tekturna HCT and other medications due to contamination with Darocur 1173, a photo-curing agent.

    Product
    Tekturna HCT (aliskiren and hydrochlorothiazide) Tablets 150/12.5 mg, 7 tablets per bottle, Physician Sample-Not For Sale, Rx only, Manufactured by: Novartis Pharma Productions GmbH Wehr, Germany. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936 , ND
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0474-2014·2013-12-18

    Synthes Trochanteric Fixation Nail Recalled for Incorrect Packaging Labeling

    Synthes USA is recalling 12 Trochanteric Fixation Nails because the packaging incorrectly lists the nail's length and diameter.

    Product
    Synthes Trochanteric Fixation Nail As part of the Synthes Trochanteric Fixation Nail (TFN) System, the TFN Nail is intended to treat stable and unstable fractures of the proximal femur.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0821-2014·2013-12-18

    Sugar-Free Corn Cake Recalled for Missing Phenylketonuria Warning

    Cakes & More Delight's is recalling sugar-free corn cakes because the packaging lacks a warning for individuals with phenylketonuria (PKU). The product contains aspartame.

    Product
    Sugar free cake: Corn. Package size: 4 oz, 12 oz
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0483-2014·2013-12-18

    Stryker Recalls Cancellous Bone Screws Due to Packaging Error

    Stryker is recalling specific Cancellous Bone Screws because a 5.5 mm screw was found in packaging labeled for a 6.5 mm screw.

    Product
    Stryker Orthopaedics Cancellous Bone Screw Howmedica Osteonics Corp. Stryker France Both the 6.4 mm diameter, 25mm length, Cancellous Bone Screws (Cat no 2030-6525-1) and the 5.5mm diameter, 40 mm length Cancellous Bone Screws (Cat no 2029-5540-1) are cleared for use in To
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0475-2014·2013-12-18

    Zimmer Trabecular Metal Total Ankle Talar Component Recall for Residue

    Zimmer, Inc. is recalling specific Total Ankle Talar Components because routine monitoring found potential elevated levels of manufacturing residue on the implants.

    Product
    Zimmer Trabecular Metal Total Ankle Talar Component Left Sizes 1-6 Total ankle arthroplasty is intended to provide a patient with limited mobility by restoring alignment, reducing pain and preserving the flexion/extension movement within the ankle joint.The Zimmer Trabecular M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0465-2014·2013-12-18

    Karl Storz Recalls Misidentified Axillent Debakey Grasping Forceps

    Karl Storz is recalling 7 units of Axillent Debakey Grasping Forceps because they were mislabeled as a different model.

    Product
    Axillent Debakey Grasping Forceps, Part No. 33821DYD In general the surgeons use 33821DYD Debakey forceps to grasp tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0822-2014·2013-12-18

    Sugar-Free Almond Cake Recalled for Missing Phenylketonuria Warning

    Cakes & More Delight's is recalling sugar-free almond cakes because the packaging lacks a required warning for individuals with phenylketonuria (PKU).

    Product
    Sugar free cake: Almond flavor. Package size:12 oz
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-328-2014·2013-12-18

    Novartis Recalls Exforge Physician Samples Due to Chemical Contamination

    Novartis is recalling Exforge physician sample bottles due to contamination with Darocur 1173, a photocuring agent found in ink.

    Product
    Exforge (amlodipine and valsartan Tablets) 5/160 mg, Rx only 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured by: Novartis Pharma Stein AG Stein, Switzerland. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936 - NDC # 0078-9488-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-330-2014·2013-12-18

    Novartis Recalls Physician Sample Blood Pressure Medications Due to Chemical Contamination

    Novartis is recalling physician sample bottles of several blood pressure and cholesterol medications due to contamination with a photocuring agent used in packaging inks.

    Product
    Exforge HCT (amlodipine, valsartan, hydrochlorothiazide) 10/320/25 mg, Rx only, 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured by: Novartis Pharma Stein AG Stein, Switzerland. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936, NDC
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-327-2014·2013-12-18

    Novartis Recalls Diovan and Other Tablets Due to Chemical Contamination

    Novartis is recalling physician sample bottles of Diovan and other tablets because they were contaminated with Darocur 1173, a photocuring agent used in inks.

    Product
    Diovan (valsartan) 320 mg per tablet, 7 Tablets per bottle, Rx only Physician Sample Not For Sale, Manufactured by: Novartis Pharmaceuticals Corporation Suffern, NY 10901 for Novartis Pharmaceuticals Corporation East Hanover, NJ 07936, NDC # 0078-9360-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-343-2014·2013-12-18

    Oxcarbazepine Tablets Recalled for Potential Subpotency

    Boehringer Ingelheim Roxane Inc. is recalling Oxcarbazepine Tablets, 150 mg, due to out-of-specification assay results and potential lower weight tablets.

    Product
    Oxcarbazepine Tablets, 150 mg, packaged in a) 10 x 10 count Unit-Dose Tablets in blisters packaged in a carton (NDC 0054-0097-20) and b) 100-count bottle (NDC 0054-0097-25), Rx only, Roxane Laboratories, Inc., Columbus, Ohio 43216
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-334-2014·2013-12-18

    Novartis Recalls Exforge Physician Samples Due to Chemical Contamination

    Novartis is recalling Exforge physician sample bottles due to contamination with Darocur 1173, a photocuring agent found in ink.

    Product
    Exforge (amlodipine and valsartan, Tablets) 10/320 mg, Rx only, 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured by: Novartis Pharma Stein AG Stein, Switzerland. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936, NDC # 0078-9491-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-333-2014·2013-12-18

    Novartis Recalls Physician Sample Blood Pressure Medications Due to Chemical Contamination

    Novartis is recalling physician sample bottles of several blood pressure medications due to contamination with a photocuring agent found in packaging inks.

    Product
    Exforge (amlodipine and valsartan Tablets) 10/160 mg, Rx only, 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured by: Novartis Pharma Stein AG Stein, Switzerland. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936, NDC # 0078-9489-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-337-2014·2013-12-18

    Novartis Recalls Physician Sample Tablets Due to Chemical Contamination

    Novartis is recalling physician sample bottles of several prescription medications, including Tekturna, due to contamination with a photocuring agent.

    Product
    Tekturna (aliskiren) Tablets 150 mg, 7 tablets per bottle, Physician Sample-Not For Sale, Rx only. Manufactured by: Novartis Pharma Productions GmbH Wehr, Germany. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936, NDC # 0078-9485-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0469-2014·2013-12-18

    Omnyx Digital Pathology Software Recalled for Incorrect Measurement Display

    Omnyx LLC is recalling Digital Pathology System (DPS) Software version 1.1 because its annotation tools may display incorrect measurements and area calculations for regions of interest on scanned slides.

    Product
    Digital Pathology System (DPS) Software version 1.1 The Omnyx" Integrated Digital Pathology system, which consists of a whole slide scanner and associated software applications, is a scanning, receiving, storing, managing, annotating and computer monitor viewing system for dig
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Drugs)·D-347-2014·2013-12-18

    Taro Recalls Subpotent Ciclopirox Shampoo 1% Prescription Bottles

    Taro Pharmaceuticals is recalling 850 bottles of Ciclopirox Shampoo 1% because the product is subpotent. The recall is voluntary and nationwide.

    Product
    CICLOPIROX — CICLOPIROX (CICLOPIROX)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0481-2014·2013-12-18

    Ultradent Recalls Avex CX2 Ceramic Orthodontic Brackets Due to Design Control Issues

    Ultradent is recalling 217 units of Avex CX2 Ceramic Orthodontic Brackets because the design control process was not completed before distribution.

    Product
    Opal Orthodontics by Ultradent. Avex CX2 Ceramic Orthodontic Brackets Avex CX2 ceramic brackets are intended for use in orthodontic treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0819-2014·2013-12-18

    Cakes & More Delight's Recalls Sugar-Free Vanilla Cakes for Missing Warning

    Cakes & More Delight's is recalling sugar-free vanilla cakes because they contain aspartame but lack the required phenylketonuria warning.

    Product
    Sugar free cake: Vanilla flavor. Package size: 4 oz, 12 oz; Sliced Sugar-free cake: Vanilla flavor 16 oz.
    Category
    Food
    Distribution
    1 state
  • SevereCPSC·14061·2013-12-17

    HP Chromebook 11 Chargers Recalled for Fire and Burn Hazards

    Google and HP are recalling HP Chromebook 11 chargers because they can overheat and melt, posing fire and burn risks.

    Product
    HP Chromebook 11 power supply/charger
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V627000·2013-12-17

    Freightliner Recalls 2013-2014 Cascadia Trucks Due to Wiring Defect

    Daimler Trucks North America is recalling 2013-2014 Freightliner Cascadia trucks because reversed wiring may reduce traction and parking brake effectiveness.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V625000·2013-12-17

    Monaco Recalls 2008-2013 RVs With Potential Door Lock Jamming Defect

    Monaco RV is recalling 3,175 recreational vehicles because a door lock defect may jam the deadbolt, potentially trapping occupants inside.

    Product
    MCKENZIE — MCKENZIE, R-VISION, HOLIDAY RAMBLER ION, SILVER CREEK, TRAIL CRUISER CLASSIC, TRAIL LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V626000·2013-12-17

    CJay Trailers Recall Cargo Trailers Due to Door Lock Jamming Risk

    CJay is recalling specific cargo trailers because a defect in the door lock may jam the deadbolt, potentially trapping occupants inside the trailer.

    Product
    CJAY — CJAY CJ714, CJ814, CJ716, CJ820
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V622000·2013-12-16

    Honda Recalls 2014 Acura RLX for Rear Suspension Bolt Issues

    Honda is recalling 7,387 2014 Acura RLX vehicles because rear suspension bolts may have loosened, potentially reducing steering ability and increasing crash risk.

    Product
    ACURA — ACURA RLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V624000·2013-12-16

    Hyundai Recalls 2014 Santa Fe Vehicles Due to Tire Sidewall Defect

    Hyundai is recalling 2014 Santa Fe vehicles equipped with specific Continental tires that may have damaged sidewalls, increasing the risk of tread detachment or rapid air loss.

    Product
    HYUNDAI — HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V633000·2013-12-16

    Thomas Built Saf-T-Liner C2 School Bus Recall for Transmission Software

    Daimler Trucks North America is recalling 2011-2013 Thomas Built Saf-T-Liner C2 school buses because transmission software may cause unintended acceleration.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES, THOMAS BUILT SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V634000·2013-12-16

    Freightliner Trucks Recalled for Transmission Software Defect

    Daimler Trucks North America is recalling 2009-2014 Freightliner trucks because transmission software may cause unintended acceleration.

    Product
    FREIGHTLINER — FREIGHTLINER MT45, BUSINESS CLASS M2, MT55
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V623000·2013-12-16

    Hino Recalls 2013 NV8J Trucks for Incorrect Weight Documentation

    Hino is recalling 2013 NV8J trucks because vehicle documents show a higher weight rating than the actual modified rating, which could lead to overloading.

    Product
    HINO — HINO NV8J
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14059·2013-12-16

    Wahl Recalls Total Care Aerosol Cleaner Due to Burn Hazard

    Wahl is recalling Total Care aerosol cleaner because vapors can ignite near hair clippers, posing a burn hazard. Three incidents were reported, including one minor burn.

    Product
    Total Care, Aerosol Cleaner, Lubricant & Coolant
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·13T012000·2013-12-12

    Michelin Recalls LTX M/S Tires Due to Tread Separation Risk

    Michelin is recalling specific LTX M/S tires due to a risk of tread separation that could lead to loss of vehicle control.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·14054·2013-12-12

    Coby 32-inch Flat Screen Televisions Recalled for Fire and Burn Hazards

    Thirteen retailers are recalling about 8,900 Coby 32-inch flat screen televisions because an electronic component can fail, catch fire, and ignite nearby items.

    Product
    Coby 32-inch flat screen televisions
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13E070000·2013-12-12

    Genera Recalls Aftermarket Tail Lights for 2012-2013 Toyota Prius V

    Genera Corporation is recalling aftermarket tail lights for 2012-2013 Toyota Prius V vehicles because the brake and tail light circuits are switched, reducing the ability to warn other drivers.

    Product
    TOYOTA — TOYOTA PRIUS V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V616000·2013-12-12

    Double R Utility Trailers Recalled for Door Lock Jamming Hazard

    Double R is recalling 2010-2014 utility trailers because a door lock defect could jam the deadbolt, potentially trapping occupants inside.

    Product
    DOUBLE R TRAILERS — DOUBLE R TRAILERS UTILITY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14055·2013-12-12

    Trek Recalls 2013 Madone Bicycles Due to Front Brake Failure Hazard

    Trek is recalling 6,800 model year 2013 Madone bicycles because the front brake can fail, posing a crash hazard. No injuries have been reported.

    Product
    Trek model year 2013 Madone bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0565-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Dairy Fresh Mexicali Pasta Salad, Product Code 0 70163 55999 8, 1/5 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0652-2014·2013-12-11

    Garden-Fresh Foods Recalls Cheesecake Delight Due to Listeria Risk

    Garden-Fresh Foods is recalling Our Own Cheesecake Delight products because they may be contaminated with Listeria monocytogenes.

    Product
    Our Own Cheesecake Delight , Product Code 0 11596 85066 5, 1/8 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0536-2014·2013-12-11

    Garden-Fresh Recalls Ready-to-Eat Salads and Dips Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Asian Vegetable Orzo,Product Code 0 11596 52073 5, 1/5 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0599-2014·2013-12-11

    Garden-Fresh Foods Recalls Creamy Tuna Salad for Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Family Style Creamy Tuna Salad, Product Code 0 11596 55108 1, 2/5 lb;
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0590-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Archer Farms Four Bean Salad, Product Code 0 85239 24207 0, 6/14 oz
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0522-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Dairy Fresh Homemade Macaroni Salad, Product Code 0 70163 89080 0, 2/5 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0636-2014·2013-12-11

    Garden-Fresh Recalls Ready-to-Eat Salads and Dips for Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Rocky Road Dessert, Product Code 0 11596 45029 2, 1/4 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0663-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads and Dips for Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Archer Farms Feta & Roasted Red Pepper Dip, Product Code 0 85239 69048 2, 6/11 oz
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0594-2014·2013-12-11

    Garden-Fresh Foods Recalls Egg Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling specific egg salad products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Egg Salad ,Product Code 0 11596 52022 3, 1/5 lb; Weis Egg Salad , Product Code 0 41497 05365 0 , 1/5 lb; Weis Egg Salad,Product Code 0 11596 55221 7, 1/5 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0496-2014·2013-12-11

    Garden-Fresh Foods Recalls Potato Salads and Slaws Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Grandpas Potato Salad, Product Code 0 11596 08005 5, 18/3.5oz.; Grandpas Potato Salad, Product Code 0 11596 14027 8, 12/16 oz.; Grandpas Potato Salad, Product Code 0 11596 24227 9, 8/2 lb.; Grandpas Potato Salad, Product Code 0 11596 34326 6, 4/3 lb.; Grandpas Potato Sala
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0574-2014·2013-12-11

    Garden-Fresh Recalls Ready-to-Eat Salads and Slaws Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Cranberry Walnut Red Cabbage Slaw, Product Code 0 11596 83028 5, 1/8.25lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0485-2014·2013-12-11

    Garden-Fresh Recalls Potato Salad Due to Listeria Contamination Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Amish Country Potato Salad, Product Code 0 11596 51005 7, 2/5lb. . .
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0412-2014·2013-12-11

    Boston Salads Recalls Seafood and Shrimp Salad for Listeria Risk

    Boston Salads & Provisions Co., Inc. is recalling Seafood and Shrimp Salad due to possible Listeria monocytogenes contamination.

    Product
    Seafood and Shrimp Salad packaged in 5 lb Sold under the label: Boston Salads
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0619-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Rogges Crab (seafood) Salad, Product Code 0 11596 55110 4, 11/1/2013 2/5 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0702-2014·2013-12-11

    Woodstock Frozen Organic Pomegranate Kernels Recalled for Hepatitis A Risk

    Scenic Fruit Co is recalling Woodstock Frozen Organic Pomegranate Kernels due to epidemiological evidence of potential hepatitis A contamination.

    Product
    Woodstock Frozen Organic Pomegranate Kernels are sold in 8 oz. (227 gram) re-sealable plastic pouches with the UPC 0 42563 01628 9. The product is labeled in parts: "***WOODSTOCK***ORGANIC POMEGRANATE KERNELS***Juicy Lil' JEWELS***USDA ORGANIC***NET WT. 8 OZ (227g)***KEEP FROZ
    Category
    Food
    Distribution
    12 states
  • CriticalFDA (Food)·F-0490-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads and Slaw for Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Knowlans Club Salad Base, Product Code 10 733147 00201 5, 1/8 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0605-2014·2013-12-11

    Garden-Fresh Foods Recalls Seafood Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Seafood Salad, 0 11596 55102 9, 1/5 lb;
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0556-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Finest Traditions Robust Pasta Salad, Product Code 10 733147 10145 9 10/30/2013 - 11/18/2013 1/8 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0666-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads and Dips for Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Finest Traditions Southwest Dip , Product Code 7 33147 10540 5, 6/8 oz Finest Traditions Southwest Dip ,Product Code 10 733147 10853 3, 1/8 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0672-2014·2013-12-11

    Garden-Fresh Foods Recalls Bagel Spread Due to Listeria Contamination Risk

    Garden-Fresh Foods is recalling Roundy's Bagel Spread and other ready-to-eat products because they may be contaminated with Listeria monocytogenes.

    Product
    Roundy's Bagel Spread, Product Code 0 11596 06156 6 11/2/2013 - 11/9/2013 6/12 oz
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0507-2014·2013-12-11

    Garden-Fresh Foods Recalls Potato Salad for Listeria Contamination

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Rogges Mustard American Potato Salad, Product Code 0 11596 51053 8, 2/5 lb;
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0706-2014·2013-12-11

    Crunch Pak Apple Slices Recalled for Listeria Contamination Risk

    Crunch Pak, LLC is recalling Blue Raspberry Flavor Sliced Apples due to potential Listeria monocytogenes contamination.

    Product
    Crunch Pak Natural Blue Raspberry Flavor Sliced Apples, 5/2 oz. bags packaged in a clamshell. The lid has a Monsters University image. The clamshell package has the UPC 7 32313 08996 9. The clamshell package is labeled in parts: "***CRUNCH PAK***flavorz***Sliced Apples with N
    Category
    Food
    Distribution
    27 states
  • CriticalFDA (Food)·F-0643-2014·2013-12-11

    Garden-Fresh Recalls Mint Chocolate Chip Cookie Mousse for Listeria Risk

    Garden-Fresh Foods is recalling Mint Chocolate Chip Cookie Mousse and other ready-to-eat products due to potential Listeria monocytogenes contamination.

    Product
    Garden-Fresh Mint Chocolate Chip Cookie Mousse, Product Code 0 11596 55069 5, 1/5 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0509-2014·2013-12-11

    Garden-Fresh Foods Recalls Potato Salad Due to Listeria Contamination Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Dairy Fresh Potato Salad With Egg, Product Code 0 70163 89085 5, 2/5 lb;
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0584-2014·2013-12-11

    Garden-Fresh Recalls Ready-to-Eat Salads and Dips Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Black Bean Couscous, Product Code 0 11596 55620 8, 1/5 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0583-2014·2013-12-11

    Garden-Fresh Recalls Ready-to-Eat Salads and Dips Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Amish Country Baked Beans, Product Code, 0 11596 55186 9, 2/5 lb;
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0487-2014·2013-12-11

    Garden-Fresh Recalls Potato Salad Products Due to Listeria Contamination Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh American Potato Salad, Product Code 0 11596 51010 1, 2/5 lb.; Garden-Fresh American Potato Salad, Product Code 0 11596 14015 5, 12/16 oz.; Garden-Fresh American Potato Salad, Product Code 0 11596 24200 2, 7 8/2 lb. ; Garden-Fresh American Potato Salad, Product
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0631-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Chopped Broccoli Cauliflower Salad Base, Product Code 0 11596 55188 3, 1/5.25lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0650-2014·2013-12-11

    Garden-Fresh Foods Recalls Pistachio Whip Due to Listeria Risk

    Garden-Fresh Foods is recalling Finest Traditions Pistachio Whip and other ready-to-eat products because they may be contaminated with Listeria monocytogenes.

    Product
    Finest Traditions Pistachio Whip, Product Code 10 733147 00020 ,1/8 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0512-2014·2013-12-11

    Garden-Fresh Foods Recalls Potato Salad Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Our Own Homestyle Mustard Potato Salad, Product Code 0 11596 51047 7, 4/5 lb; ;
    Category
    Food
    Distribution
    10 states

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