The Recall Desk

Archive

June 2015 recalls

481 recalls were announced in June 2015.

What the numbers show

Critical
29
Severe
142
High
216
Moderate
74
Low
20

Of the 481 recalls this month scored against our rubric, 6% are Critical, 30% are Severe.

Which agencies issued them

201–300 of 481

  • HighFDA (Devices)·Z-1714-2015·2015-06-17

    ASP Recalls EVOTECH Endoscope Cleaner for Connection Detection Failure

    Advanced Sterilization Products is recalling EVOTECH Endoscope Cleaner and Reprocessor units because they may fail to detect disconnected endoscopes, allowing the cleaning cycle to complete without proper processing.

    Product
    EVOTECH Endoscope Cleaner and Reprocessing System 208V, P/N 50004. The ASP EVOTECH ECR Endoscope Cleaner and Reprocessor is a washer/disinfector, which is indicated for use with high-level disinfectant CIDEX OPA Concentrate and an enzymatic detergent (CIDEZYME Gl) to achieve…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1763-2015·2015-06-17

    Philips Brilliance CT 40 Uninterruptible Power Supply Recall

    Philips is recalling Brilliance CT 40 Uninterruptible Power Supply accessories due to risks of battery acid leakage, overheating, and fume emission.

    Product
    Brilliance CT 40 - Slices(Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1788-2015·2015-06-17

    Philips Recalls GEMINI TF Ready UPS Accessory Devices for CT Systems

    Philips Medical Systems is recalling three GEMINI TF Ready UPS accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fumes.

    Product
    GEMINI TF Ready (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1758-2015·2015-06-17

    Edwards Lifesciences IntraClude Intra-Aortic Occlusion Device Recalled for Potential Damage

    Edwards Lifesciences is recalling IntraClude Intra-Aortic Occlusion Devices due to potential damage near the hub that may cause blood leakage.

    Product
    Edwards Lifesciences IntraClude Intra-Aortic Occlusion Device, model number ICF100, 10.5 Fr (3.5 mm) x 39.4" (100 cm) ThruPort System. Packaged sterile and non-pyrogenic in a sealed, peel-type pouch For use in patients undergoing cardiopulmonary bypass.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1719-2015·2015-06-17

    Elekta Recalls Leksell GammaPlan Software Due to Memory Corruption

    Elekta is recalling 10 units of Leksell GammaPlan 10.2 software because memory can become corrupted when creating a fused study via drag and drop.

    Product
    Laksell GammaPlan, a computer based dose planning system specifically designed for use with Leksell Gamma Knife, radiation therapy treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1768-2015·2015-06-17

    Philips Brilliance iCT UPS Accessory Devices Recalled for Battery Acid Leakage

    Philips Medical Systems is recalling Brilliance iCT UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.

    Product
    Brilliance iCT (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1774-2015·2015-06-17

    Philips FORTE UPS Accessory Devices Recalled for Battery Acid Leakage Risk

    Philips Medical Systems is recalling 10 FORTE Uninterruptible Power Supply (UPS) accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.

    Product
    FORTE (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1741-2015·2015-06-17

    Biomet Recalls Unilateral External Fixation Ankle Clamps Due to Assembly Error

    Biomet, Inc. is recalling 19 unilateral external fixation ankle clamps because they were assembled incorrectly. The defect may prevent full range of motion and cause the pin to loosen from the bone.

    Product
    Unilateral external fixation ankle clamp Product Usage: Unilateral external fixation for use treatment of bone conditions amenable to treatment by use of external fixation modality
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1725-2015·2015-06-17

    Abbott Alkaline Wash Recall Due to Cap Leaking and Crystallization

    Abbott Laboratories is recalling Alkaline Wash cleaning solution for Abbott Architect analyzers due to product leaking from the cap and crystallization around the cap.

    Product
    Alkaline Wash, List number 9D31-20, a cleaning solution used by the Abbott Architect analyzers. It is supplied in 500 mL bottles and contains NaOCl, NaOH, and KOH. It is shipped and stored at room temperature and is shipped ready to use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1718-2015·2015-06-17

    Advanced Back Technologies Recalls Extentrac Elite User Manual

    Advanced Back Technologies is recalling 18 Extentrac Elite User Manuals because they incorrectly state the device is for patients up to 350 lbs, while the device is only approved for up to 300 lbs.

    Product
    Extentrac Elite User Manual DCN: 14-001 (Powered decompression table, for traction)
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-1749-2015·2015-06-17

    Orthofix Firebird Spinal Fixation System Recalled for Mislabeling

    Orthofix is recalling Firebird Spinal Fixation System screws because the length marking on the tip is incorrect.

    Product
    ORTHOFIX Firebird Spinal Fixation System 6.5mm x 55mm Multi-Axial Screw, Standard Implant Grade Titanium Alloy Rx Only Provided Non-Sterile Do Not Reuse
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Food)·F-2406-2015·2015-06-17

    Rugby Poly Vitamin Liquid Recalled for Packaging Label Mismatch

    Pharmatech LLC is recalling Rugby Poly Vitamin Liquid with Iron because the outside packaging labels may not match the individual product labeling, potentially displaying incorrect lot, expiration, or product identity information.

    Product
    Rugby Poly Vitamin Liquid with Iron, 50 ml
    Category
    Drug
    Distribution
    37 states
  • ModerateFDA (Food)·F-2409-2015·2015-06-17

    Nuevotanicals Recalls Kratom Oil Products Due to Kratom Content

    Nuevotanicals is recalling Kratom (Kr8om) MD Oil products because they contain Kratom. The recall covers units distributed across 12 states.

    Product
    Kratom (Kr8om) MD (Maeng Da Thai) Oil in 225 mg., 375 mg., and 150 mg. dosages.
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Drugs)·D-1133-2015·2015-06-17

    SCA Pharmaceuticals Recalls Phenylephrine Bags Due to Labeling Error

    SCA Pharmaceuticals is recalling 50 bags of phenylephrine HCl 50 mg in 0.9% sodium chloride due to a label mix-up. The product was incorrectly labeled instead of phenylephrine in 5% dextrose.

    Product
    PHENYLephrine HCl 50 mg in 0.9% Sodium Chloride 250 mL bag (Concentration = 0.2 mg per mL), Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR (877) 550-5059, barcode 88888772029.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-2417-2015·2015-06-17

    Nuevotanicals Recalls Unlabeled Kratom Leaf Powder Products

    Nuevotanicals is recalling unlabeled Kratom leaf powder products because they contain Kratom.

    Product
    Enhanced Leaf Powder in Ziploc-type freezer bags in 500 g increments, no product label; Bulk Raw (non-extracted) Kratom Leaf Powder in Ziploc-type freezer bags in 500 g increments, no product label.
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-1638-2015·2015-06-17

    GE OEC Brivo 865 Plus Mobile X-ray Laser Aimer Assemblies Recalled

    GE OEC Medical Systems is recalling nine mobile X-ray laser aimer assemblies because they were shipped without required laser product certification.

    Product
    GE OEC Brivo 865 plus, Mobile X-ray system laser aimer assemblies (part number 520002DW)
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1729-2015·2015-06-17

    Ortho-Clinical Diagnostics Recalls VITROS Urine Assay Data Disks

    Ortho-Clinical Diagnostics is recalling VITROS Urine Assay Data Disks because a software error may allow samples requiring acidified pretreatment to be metered from the same container as those requiring no pretreatment.

    Product
    Assay Data Disk (ADD), All DRV versions that support product within expiry dating Automates pre-analytical and post-analytical sample and data management for in vitro diagnostic use. VITROS Urine Assays: VITROS Calcium (Ca), Magnesium (Mg), and Phosphorus (Phos) requires…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1116-2015·2015-06-17

    Valeant Recalls Nifedipine Extended-Release Tablets Due to Dissolution Failures

    Valeant Pharmaceuticals is recalling Nifedipine Extended-Release Tablets, 90 mg, because some lots failed dissolution specifications.

    Product
    Nifedipine Extended-Release Tablets, USP, 90 mg, 100 Tablet Bottles, Rx Only. Manufactured for: Teva Pharmaceuticals USA Sailorsville, PA 13960. Manufactured in Canada By: Valeant Pharmaceuticals International, Inc. Steinbach, MB R5G 127 Canada. NDC: 0093-2059-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1129-2015·2015-06-17

    Akorn Recalls Hydroxyzine Hydrochloride Oral Solution Due to Impurity Failures

    Akorn, Inc. is recalling 424,174 bottles of Hydroxyzine Hydrochloride oral solution because the product failed impurities and degradation specifications.

    Product
    Hydroxyzine Hydrochloride, oral solution, 10 mg per 5 mL, 16 fl oz (473 ml) bottle, Rx only, Manufactured for KVK-Tech, Inc., Newtown, PA by Hi-Tech Pharmacal Co., Inc., Amityville, NY, NDC 10702-0052-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·093-2015·2015-06-17

    Pinnacle Foods Recalls Swanson Turkey Dinners for Undeclared MSG

    Pinnacle Foods is recalling approximately 668,316 pounds of Swanson Stuffing Baked Turkey dinners because the product contains monosodium glutamate (MSG) that is not declared on the label.

    Product
    Recall Notification Report 093-2015 (Poultry Products )
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1132-2015·2015-06-17

    Mallinckrodt Recalls MD Gastroview Due to Labeling Errors

    Mallinckrodt is recalling 6,600 bottles of MD Gastroview because some bottles have incorrect or missing lot numbers and expiration dates.

    Product
    MD GASTROVIEW — MD GASTROVIEW (DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM)
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Food)·F-2411-2015·2015-06-17

    Nuevotanicals Recalls K SHOT Kratom Supplement Due to Kratom Content

    Nuevotanicals is recalling K SHOT botanical supplement shots because the products contain Kratom. The recall affects 10,000 units distributed across 12 states.

    Product
    K SHOT 0.5 fl. oz (15 ml) 9 GRAMS OF HIGH QUALITY KRATOM LEAF PER BOTTLE Botanical Supplement Shot 100% Natural PURE ALKALOID CONCENTRATE OIL 100% NATURAL Vegan, Kosher, Halal, and Ital friendly
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-1717-2015·2015-06-17

    Extentrac Elite Powered Decompression Table Recalled for Weight Limit Mislabeling

    Advanced Back Technologies is recalling 36 Extentrac Elite powered decompression tables because the product brochure incorrectly states a 350-lb weight limit, while the device is only approved for patients up to 300 lbs.

    Product
    Extentrac Elite product brochure DCN: 13-001, 09-001 (Powered decompression table, for traction)
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Food)·F-2415-2015·2015-06-17

    FDA Recalls Unlabeled Green Malay Kratom Bulk Product

    The FDA is recalling 77 kg of unlabeled Green Malay Kratom bulk product in 1-gallon jugs due to the presence of Kratom.

    Product
    Green Malay/MD bulk in 1 gallon plastic jugs, no product label
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-1746-2015·2015-06-17

    Becton Dickinson Recalls BBL Port A Cul Tubes Due to Oxidation

    Becton Dickinson is recalling BBL Port A Cul tubes because excessive oxidation may affect the viability of anaerobic microorganisms.

    Product
    BBL Port A Cul tubes, catalog number 221606. Patient sample collection tubes. BBL Port A Cul tubes, jars and vials contain a reduced transport medium and are intended to maintain the viability of anaerobic, facultative and aerobic microorganisms during transport from the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2420-2015·2015-06-17

    Roxy Trading Recalls Seasoning Fish Filet for Mislabeling and Missing Ingredients

    Roxy Trading Inc. is recalling Seasoning Fish Filet because the label incorrectly identifies the fish as Grouper and omits the full ingredient list.

    Product
    Seasoning Fish Filet Ingredients: Mixed Fish, Sugar, Salt, Monosodium Glutamate, Sorbic Acid Bulk cases with 12kg of fish fillets which are packaged in clear plastic. The label does not declare the type of fish, other ingredients in the product, or nutrition facts.
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-2416-2015·2015-06-17

    Nuevotanicals Recalls Unlabeled Kratom Powder in Freezer Bags

    Nuevotanicals is recalling 326 kg of unlabeled Kratom powder in 500 g freezer bags distributed to 12 states.

    Product
    Max powder in Ziploc-type freezer bags in 500 g increments, no product label
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Food)·F-2405-2015·2015-06-17

    Rugby Poly Vitamin Liquid Recalled for Packaging Label Mismatch

    Pharmatech LLC is recalling Rugby Poly Vitamin Liquid, 50ml, because the outside packaging may have incorrect lot, expiration, or product identity information.

    Product
    Rugby Poly Vitamin Liquid, 50ml
    Category
    Drug
    Distribution
    37 states
  • ModerateFDA (Devices)·Z-1720-2015·2015-06-17

    Roscoe Mini Neb Compressor User Manual Recall for Warning Updates

    Compass Health Brands is recalling 219,353 Roscoe Mini Neb Compressor user manuals to add warnings about proper handling and storage to reduce power cord damage.

    Product
    Roscoe Mini Neb Compressor User Manual for the NEB-ROS Product Usage: Inhaler therapy that converts liquid medicine into a fine mist that is easily inhaled.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1754-2015·2015-06-17

    Biomet Recalls Hip Components Due to Incorrect GTIN Labeling Codes

    Biomet is recalling specific hip joint replacement components because the device labeling contains incorrect Global Trade Identification Number (GTIN) codes.

    Product
    Mallory/Head Primary Hip System; Size 11, 160 mm, Lateralized Femoral Stem; Ti-6Al-4V; Porous Plasma Uncemented, & Mallory/Head Total Hip System Size 12, 165 mm, Bi- Metric Femoral Components. Hip joint replacement components include: femoral stems, femoral heads, acetabular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1755-2015·2015-06-17

    Biomet Shoulder Joint Replacement Components Recalled for Incorrect GTIN Codes

    Biomet, Inc. is recalling specific shoulder joint replacement components because the device labeling contains incorrect Global Trade Identification Number (GTIN) codes.

    Product
    Comprehensive Shoulder System, 4 mm, 122 mm long, Primary Shoulder Stem, Ti-6Al-4V, Standard Length Porous Plasma. Shoulder joint replacement components include humeral stems, humeral heads, and glenoid components.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1740-2015·2015-06-17

    Acclarent Recalls Expired RELIEVA FLEX Sinus Guide Catheter Units

    Acclarent, Inc. is recalling 986 RELIEVA FLEX Sinus Guide Catheter units distributed in Texas because one unit was found to be past its expiry date.

    Product
    RELIEVA FLEX Sinus Guide Catheter F-70. Catalog number GC070RF. Product Usage - Sinus Catheter - Intended to provide a means to access the sinus space for diagnostic and therapeutic procedures. .
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Food)·F-2419-2015·2015-06-17

    Mothers' Milk Bank of Montana Recalls Breast Milk Due to Plastic Fragment

    Mothers' Milk Bank of Montana is recalling 63 bottles of breast milk because a plastic fragment was found in one bottle. The product was distributed in Montana and Washington.

    Product
    Mother's Milk was labeled as "Mature milk". This is breast milk and was donated from nursing mothers. Product is packaged in glass bottle, 4 oz. The logo of Mother's Milk Bank is observed on a label. All milk was shipped frozen.
    Category
    Food
    Distribution
    2 states
  • LowFDA (Devices)·Z-1756-2015·2015-06-17

    Biomet Knee Joint Replacement Components Recalled for Incorrect GTIN Codes

    Biomet is recalling MCK Maximum Congruent Knee System components because the device labeling contains incorrect Global Trade Identification Number (GTIN) codes.

    Product
    MCK Maximum Congruent Knee System, BIOMET FINNED PRI STEM 40MM; 80 x 10MM; 80 x 12.5 MM; 80 x 15 MM Knee joint replacement prostheses components include femoral, tibial, and patellar components.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1757-2015·2015-06-17

    Biomet Recalls Hip Joint Components Due to Incorrect GTIN Labeling

    Biomet is recalling 1,315 hip joint replacement components because the device labeling contains incorrect Global Trade Identification Number (GTIN) codes.

    Product
    Biomet Cobalt-Chrome Femoral Components, 32MM MOD HEAD COCR -6MM NECK; 32MM MOD HEAD COCR -3 MM NECK; 32MM MOD HEAD COCR STD NECK ; 32MM MOD HEAD COCR +3MM NECK; 32MM COCR MOD HD +6MM NO SKIRT Hip joint replacement components include: femoral stems, femoral heads, acetabular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V376000·2015-06-16

    EverGreen Recalls 2015 Travel Trailers Due to Wheel Stud Defect

    EverGreen is recalling 2015 i-Go, Ever-Lite, Sun Valley, and Ascend travel trailers because wheel studs may break, potentially causing the wheel to detach.

    Product
    EVERGREEN — EVERGREEN EVER-LITE, I-GO, ASCEND, SUN VALLEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V378000·2015-06-16

    Great Dane Recalls 2015 Converter Dollies Due to Brake Valve Defect

    Great Dane is recalling 111 model year 2015 Converter Dolly trailers because a brake valve defect may cause brake drag, leading to overheating, fire, or wheel detachment.

    Product
    GREAT DANE — GREAT DANE CONVERTER DOLLY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V379000·2015-06-16

    Vactor and Guzzler Vacuum Trucks Recalled for Boiler Assembly Defect

    Vactor is recalling 2014-2015 HXX and 2100 Plus trucks, and Guzzler Guzzcavator trucks, because incorrect boiler assembly hardware may cause the unit to detach, increasing crash risk.

    Product
    GUZZLER — GUZZLER, VACTOR GUZZCAVATOR, 2100 PLUS, HXX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15165·2015-06-16

    Bunnies by the Bay Recalls Pull Toys Due to Choking Hazard

    Bunnies by the Bay is recalling Bud and Skipit Wheely Cute Pull Toys because wheel hub caps can break off, posing a choking hazard to young children.

    Product
    Bud and Skipit Wheely Cute Pull Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·092-2015·2015-06-16

    Venus Foods Recalls Pork Sausage for Undeclared Wheat Allergen

    Venus Foods Inc. is recalling approximately 25,380 pounds of pork sausage products because they contain wheat, a known allergen, that is not declared on the label.

    Product
    Venus Foods Inc. — Venus Foods Inc Recalls Pork Sausage Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·15V377000·2015-06-16

    EverGreen Recalls Fifth Wheel Trailers Due to Step Rivet Failure Risk

    EverGreen is recalling 2014-2016 fifth wheel trailers because a rivet on the entry steps may shear, causing the steps to give and increasing the risk of injury.

    Product
    EVERGREEN — EVERGREEN LIFESTYLE, ALPHA GOLD, BAY HILL, TESLA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·091-2015·2015-06-15

    Fresca Italia Recalls Pork Products Lacking Import Inspection

    Fresca Italia Inc is recalling approximately 36 pounds of pork products produced in Italy that were not inspected at the U.S. point of entry.

    Product
    Fresca Italia Inc Recalls Pork Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·15V370000·2015-06-15

    Honda Recalls Vehicles for Passenger Air Bag Inflator Rupture Risk

    Honda is recalling specific 2001-2007 models because the passenger air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    HONDA — HONDA, ACURA CIVIC, ACCORD, CIVIC GX, CIVIC HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V375000·2015-06-15

    Newmar Recalls 2015 King Aire and Essex for Suspension Defect

    Newmar is recalling 2015 King Aire and Essex vehicles because tag axle suspension hangers may move, increasing crash risk.

    Product
    NEWMAR — NEWMAR KING AIRE, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V373000·2015-06-15

    Volkswagen Recalls 2015 Passat Vehicles for Brake Line Tightening Issue

    Volkswagen is recalling 2015 Passat vehicles because a brake line may not be properly tightened, potentially causing fluid leaks and reduced braking performance.

    Product
    VOLKSWAGEN — VOLKSWAGEN PASSAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V374000·2015-06-15

    New Horizons Recalls 2013-2015 Summit and Majestic RVs for Step Defect

    New Horizons is recalling 2013-2015 Summit and Majestic RVs because a rivet on the quad entry steps may fail, causing the steps to give and increasing the risk of injury.

    Product
    NEW HORIZONS — NEW HORIZONS MAJESTIC, SUMMIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E051000·2015-06-15

    Alcoa Recalls 22.5-Inch Aluminum Wheels Due to Forging Defect

    Alcoa is recalling specific 22.5-inch aluminum wheels manufactured in April and May 2015 because a forging defect may cause the rim flange to separate during tire mounting.

    Product
    WHEELS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E049000·2015-06-12

    Yakima Recalls Q-Tower Roof Racks Due to Loose Fit Risk

    Yakima is recalling specific Q-Tower Roof Racks and replacement towers because clamping wedges may slide, causing a loose fit that could eject the rack while driving.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V366000·2015-06-12

    Subaru Recalls 2015-2016 Models for Driver Assist System Defect

    Subaru is recalling specific 2015-2016 models because a faulty switch may prevent the automatic pre-collision braking system from functioning, increasing crash risk.

    Product
    SUBARU — SUBARU XV CROSSTREK, OUTBACK, LEGACY, WRX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·090-2015·2015-06-12

    Larry's Custom Meats Recalls Beef Tongue Products Containing Specified Risk Materials

    Larry's Custom Meats Inc. is recalling beef tongue products that may contain lingual tonsils, which are specified risk materials for BSE.

    Product
    Trinity Meat Company LLC — Larry's Custom Meats Inc. Recalls Beef Tongue Products That May Contain Specified Risk Materials
    Category
    Food
    Distribution
    2 states
  • HighCPSC·15161·2015-06-11

    Tri-Vista Monogram Beverage Mugs Recalled Due to Microwave Fire Hazard

    Tri-Vista Designs is recalling about 10,000 metallic monogram beverage mugs sold at Kirkland's because they can spark in the microwave, posing a fire hazard.

    Product
    Metallic Monogram Beverage Mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15163·2015-06-11

    Ramart Recalls Swing Chairs Due to Fall Hazard

    Ramart is recalling apple and teardrop-shaped swing chairs sold at HomeGoods because they can tip over, posing a fall hazard.

    Product
    Swing chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2368-2015·2015-06-10

    Frontier Vegetarian Broth Powder Recalled for Salmonella Contamination Risk

    Frontier Natural Products Co-op is recalling specific lots of Vegetarian Broth Powder due to potential Salmonella contamination. The product was distributed nationwide, to Puerto Rico, the Virgin Islands, Canada, and military channels.

    Product
    Frontier Natural Products Co-Op Vegetarian Broth Powder No - Chicken Certified Organic. The responsible name on the package is Frontier Norway, IA. The product is packaged in the following configurations: (1) Foil packet, Net 453 g 16 oz, UPC 0 89836 02869 3; and (2)…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2374-2015·2015-06-10

    Frontier Chipotle Black Bean Dip Mix Recalled for Salmonella Risk

    Frontier Natural Products Co-op is recalling Simply Organic Chipotle Black Bean Dip Mix due to potential Salmonella contamination.

    Product
    Simply Organic Chipotle Black Bean Dip Mix Certified Organic packaged in foil lined paper packet Net Wt. 1.13 OZ. (32 g), UPC 0 89836 15714 0. The responsible name on the package is Frontier Natural Products Co-op Norway, IA.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2378-2015·2015-06-10

    Frontier Simply Organic Alfredo Sauce Mix Recalled for Salmonella Risk

    Frontier Natural Products Co-op is recalling Simply Organic Alfredo Sauce Mix packets due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Simply Organic Alfredo Sauce Mix Certified Organic packaged in foil lined paper packet Net Wt. 1.48 OZ. (41 g), UPC 0 89836 18544 0. The responsible name on the package is Frontier Natural Products Co-op Norway, IA.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2376-2015·2015-06-10

    Frontier Organic Spaghetti Sauce Mix Recalled for Salmonella Risk

    Frontier Natural Products Co-op is recalling Simply Organic Roasted Garlic Spaghetti Sauce Mix due to potential Salmonella contamination.

    Product
    Simply Organic Roasted Garlic Spaghetti Sauce Mix Certified Organic packaged in foil lined paper packet Net Wt. 1.13 OZ. (32 g), UPC 0 89836 18543 3. The responsible name on the package is Frontier Natural Products Co-op Norway, IA.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2371-2015·2015-06-10

    Frontier Organic Ranch Dip Mix Recalled for Salmonella Contamination Risk

    Frontier Natural Products Co-op is recalling specific lots of organic ranch dip and dressing mix due to potential Salmonella contamination.

    Product
    Ranch Dip / Dressing Mix Certified Organic packaged the following containers under multiple labels: Frontier Natural Products Co-Op foil packet Net 453 g 16 oz, UPC 0 89836 02926 3; Simply Organic foil-lined paper packet Net Wt. 1.00 oz (28 g), UPC 0 89836 18833 5; and Simply…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2380-2015·2015-06-10

    Frontier Simply Organic Fajita Seasoning Recalled for Salmonella Contamination

    Frontier Natural Products Co-op is recalling Simply Organic Fajita Seasoning packets due to potential Salmonella contamination. The product was distributed nationwide, to Puerto Rico, the Virgin Islands, Canada, and military channels.

    Product
    Simply Organic Fajita Seasoning Certified Organic packaged in foil lined paper packet Net Wt. 1.0 OZ. (28 g), UPC 0 89836 18535 8. The product is also marketed under a French/English label Net Wt. 28 g, UPC 0 89836 20002 0. The responsible name on the package is Frontier…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2381-2015·2015-06-10

    Frontier Simply Organic Vegetarian Chili Seasoning Recalled for Salmonella Contamination

    Frontier Natural Products Co-op is recalling Simply Organic Vegetarian Chili Seasoning due to potential Salmonella contamination. The product was distributed nationwide, to Puerto Rico, the Virgin Islands, Canada, and military channels.

    Product
    Simply Organic Vegetarian Chili Seasoning Certified Organic packaged in foil lined paper packet Net Wt. 1.0 OZ. (28 g), UPC 0 89836 18536 5. The product is also marketed under a French/English label Net Wt. 28 g, UPC 0 89836 18870 0. The responsible name on the package is…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2384-2015·2015-06-10

    Frontier Organic French Onion Dip Mix Recalled for Salmonella Risk

    Frontier Natural Products Co-op is recalling Simply Organic French Onion Dip Mix packets due to potential Salmonella contamination. The product was distributed nationwide, to Puerto Rico, the Virgin Islands, Canada, and military channels.

    Product
    Simply Organic French Onion Dip Mix Certified Organic packaged in foil lined paper packet Net Wt. 1.10 OZ. (31 g), UPC 0 89836 18841 0. The product is also marketed under a French/English label Net Wt. 31 g, UPC 0 89836 18878 6. The responsible name on the package is Frontier…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2373-2015·2015-06-10

    Frontier Italian Herb Spaghetti Sauce Mix Recalled for Salmonella Risk

    Frontier Natural Products Co-op is recalling Simply Organic Italian Herb Spaghetti Sauce Mix because it may be contaminated with Salmonella.

    Product
    Simply Organic Italian Herb Spaghetti Sauce Mix Certified Organic packaged in foil lined paper packet Net Wt. 1.31 OZ. (37 g), UPC 0 89836 15710 2. The responsible name on the package is Frontier Natural Products Co-op Norway, IA.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2345-2015·2015-06-10

    Kroger Raw Macadamia Nuts Recalled Due to Salmonella Test Results

    The Kroger Company is recalling 21-pound cases of Raw #4 Macadamia Nuts after the FDA reported positive Salmonella test results. The product was distributed to Georgia.

    Product
    Kroger Raw #4 Macadamia Nut, Dist. by the Kroger Company Cincinnati, Ohio 2 04192 50867 6
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-2367-2015·2015-06-10

    Frontier Organic Vegetable Broth Powder Recalled for Salmonella Risk

    Frontier Natural Products Co-op is recalling specific lots of Low Sodium Broth Powder Vegetable Flavored due to potential Salmonella contamination.

    Product
    Frontier Natural Products Co-Op Low Sodium Broth Powder Vegetable Flavored Certified Organic packaged in a foil packet, Net 453 g 16 oz, UPC 0 89836 02780 1. The responsible name on the package is Frontier Norway, IA.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2377-2015·2015-06-10

    Frontier Organic Caesar Dressing Recalled for Salmonella Contamination

    Frontier Natural Products Co-op is recalling Simply Organic Classic Caesar Dressing packets due to potential Salmonella contamination.

    Product
    Simply Organic Classic Caesar Dressing Certified Organic packaged in foil lined paper packet Net Wt. 1.25 OZ. (35 g), UPC 0 89836 18836 6. The responsible name on the package is Frontier Natural Products Co-op Norway, IA.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2364-2015·2015-06-10

    Frontier Garlic Powder Recalled Due to Salmonella Contamination Risk

    Frontier Natural Products Co-op is recalling specific lots of Garlic Powder because the product may be contaminated with Salmonella.

    Product
    Frontier Natural Products Co-Op Garlic Powder, Certified Organic, Non-Irradiated with responsible firm name Frontier Norway, IA packaged in the following configurations: (1) Foil packet labeled Powdered Garlic Allium sativum, Net 453 g 16 oz. UPC code 0 89836 00352 2; (2)…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2350-2015·2015-06-10

    Schnucks Recalls Chef's Express California Pasta Salad Due to Salmonella Risk

    Schnucks Markets is recalling Chef's Express California Pasta Salad because it may be contaminated with Salmonella. The product was sold in Schnucks stores in five states.

    Product
    Pasta salad sold under the brand name CHEF'S EXPRESS CALIFORNIA PASTA SALAD, UPC 2 10612 30070 6. Product is sold by weight through firm's Deli / Chef's Express department in plastic containers. Variable weight item. The responsible name on the label is Schnucks St. Louis…
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·15V365000·2015-06-10

    Rush Recalls Modified Peterbilt Trucks Due to Seat Belt Anchor Defect

    Rush Truck Centers is recalling modified Peterbilt 337, 348, and 382 trucks because seat belt anchorages may come unanchored under load, increasing injury risk in a crash.

    Product
    PETERBILT — PETERBILT 348, 337, 382
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2187-2015·2015-06-10

    Giant Eagle Apricot Filled Cookies Recalled for Undeclared Milk Allergen

    Giant Eagle is recalling Apricot Filled Cookies sold over the counter because the labels failed to declare the milk allergen.

    Product
    Apricot Filled Cookie OTC Sell By: (all dates up to) 3/23/2015 Net WT. 1 OZ Contains:Egg, Wheat, Soy ; Cookies affected are only sold direct from bakery counter and packaged at time per customer request and packed either in clam shell plastic or wax paper. ; Net Weight…
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1711-2015·2015-06-10

    Synthes Cannulated Drill Bits Recalled for Potential Breakage During Use

    Synthes, Inc. is recalling specific lots of Cannulated Drill Bits because they have the potential to break during use. The affected devices were distributed in the US and Canada.

    Product
    3.2 mm Cannulated Drill Bit/ QC 170 mm 2.7 Cannulated Drill Bit/ QC 160 mm 2.0 mm Cannulated Drill Bit / QC 150 mm there is no indication for Synthes Cannulated Drill Bits which is used with the Synthes Cannulated Screw. The Synthes Cannulated Screw, used with the threaded…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2382-2015·2015-06-10

    Frontier Simply Organic Spicy Chili Seasoning Recalled for Salmonella Risk

    Frontier Natural Products Co-op is recalling Simply Organic Spicy Chili Seasoning because it may be contaminated with Salmonella.

    Product
    Simply Organic Spicy Chili Seasoning Certified Organic packaged in foil lined paper packet Net Wt. 1.0 OZ. (28 g), UPC 0 89836 18537 2 The product is also marketed under a French/English label Net Wt. 28 g, UPC 0 89836 18871 7. The responsible name on the package is Frontier…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2372-2015·2015-06-10

    Frontier Organic Black Peppercorns with Garlic Recalled for Salmonella Risk

    Frontier Natural Products Co-op is recalling specific lots of organic black peppercorns with garlic due to potential Salmonella contamination.

    Product
    Frontier Natural Products Co-Op Pepper Fusion Black Peppercorns with Garlic Certified Organic packaged in a glass bottle Net Wt. 1.76 OZ. (50 g), UPC 0 89836 19502 9. The responsible name on the package is Frontier Norway, IA.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2383-2015·2015-06-10

    Frontier Organic Sweet Basil Pesto Sauce Mix Recalled for Salmonella Risk

    Frontier Natural Products Co-op is recalling Simply Organic Sweet Basil Pesto Sauce Mix packets because they may be contaminated with Salmonella.

    Product
    Simply Organic Sweet Basil Pesto Sauce Mix Certified Organic packaged in foil lined paper packet Net Wt. 0.53 OZ. (15 g), UPC 0 89836 18542 6. The product is also marketed under a French/English label Net Wt. 15 g, UPC 0 89836 20004 4. The responsible name on the package is…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2362-2015·2015-06-10

    Amy's Gluten Free Vegetable Lasagna Recalled for Listeria Risk

    Amy's Kitchen is recalling specific lots of Gluten Free Dairy Free Vegetable Lasagna because a spinach supplier notified them that the ingredient contained Listeria monocytogenes.

    Product
    Amy's Gluten Free Dairy Free Vegetable Lasagna, 9.0 oz (255 g) 12 boxes per case. UPC: 0-42272-00814-8 US distribution only; UPC: 0-42272-90814-1, Canadian distribution UPC : 0-42272-90807-3 - Canadian distribution Amy Kitchen, Petaluma, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2370-2015·2015-06-10

    Frontier Organic Mama Garlic Recalled Due to Salmonella Contamination Risk

    Frontier Natural Products Co-op is recalling 1,374 canisters of Organic Mama Garlic due to potential Salmonella contamination. The product was distributed nationwide, to Puerto Rico, the Virgin Islands, Canada, and military channels.

    Product
    Frontier Natural Products Co-Op Organic Mama Garlic packaged in a cardboard canister with paper label Net Wt. 5 oz (141 g), UPC 0 89836 18506 8. The responsible name on the package is Frontier Norway, IA.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E048000·2015-06-10

    ZF Recalls Bus Hub Carriers Due to Casting Porosity and Leak Risk

    ZF Group is recalling certain bus hub carriers manufactured between January 2014 and June 2015. Casting defects may cause oil leaks or cracks, potentially leading to hub failure and loss of vehicle control.

    Product
    POWER TRAIN:AXLE HUBS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V364000·2015-06-10

    Nissan Recalls 2015 Murano Vehicles for ABS Actuator Defect

    Nissan is recalling 2015 Murano vehicles because contaminated ABS actuators may cause loss of vehicle stability and increase crash risk.

    Product
    NISSAN — NISSAN MURANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2356-2015·2015-06-10

    Amy's Spinach Pizza Recalled Due to Listeria Monocytogenes Contamination

    Amy's Kitchen is recalling Spinach Pizza because a supplier notified them that the spinach used was contaminated with Listeria Monocytogenes.

    Product
    Amy's Spinach Pizza 14.0 oz (397 g) 8 boxes per case. UPC: 0-42272-00102-6, US distribution only Amy Kitchen, Petaluma, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2366-2015·2015-06-10

    Frontier Refried Pinto Beans Mix Recalled for Salmonella Contamination

    Frontier Natural Products Co-op is recalling specific lots of Refried Pinto Beans Mix due to potential Salmonella contamination. Consumers should check their pantry and stop using the product.

    Product
    Frontier Natural Products Co-Op Refried Pinto Beans Mix Certified Organic packaged in a foil packet, Net 453 g 16 oz, UPC 0 89836 02762 7. The responsible name on the package is Frontier Norway, IA.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2385-2015·2015-06-10

    Frontier Guacamole Dip Mix Recalled for Salmonella Contamination Risk

    Frontier Natural Products Co-op is recalling Simply Organic Guacamole Dip Mix due to potential Salmonella contamination. The product was distributed nationwide, to Puerto Rico, the Virgin Islands, Canada, and military channels.

    Product
    Simply Organic Guacamole Dip Mix Certified Organic packaged in foil lined paper packet Net Wt. 0.80 OZ. (22 g), UPC 0 89836 18842 7. The product is also marketed under a French/English label Net Wt. 22 g, UPC 0 89836 18879 3. The responsible name on the package is Frontier…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2369-2015·2015-06-10

    Frontier Organic Onion Soup Mix Recalled for Salmonella Contamination Risk

    Frontier Natural Products Co-op is recalling specific lots of Organic Onion Soup & Dip Mix due to potential Salmonella contamination. Consumers should check their packets against the listed lot numbers.

    Product
    Frontier Natural Products Co-Op Onion Soup & Dip Mix Certified Organic packaged in a foil packet, Net 453 g 16 oz, UPC 0 89836 02918 8. The responsible name on the package is Frontier Norway, IA.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2379-2015·2015-06-10

    Frontier Simply Organic Enchilada Sauce Seasoning Recalled for Salmonella Risk

    Frontier Natural Products Co-op is recalling Simply Organic Enchilada Sauce Seasoning packets due to potential Salmonella contamination. The product was distributed nationwide, to Puerto Rico, the Virgin Islands, Canada, and military channels.

    Product
    Simply Organic Enchilada Sauce Seasoning, Certified Organic, packaged in foil lined paper packet Net Wt. 1.41 OZ. (40 g), UPC 0 89836 18744 4. The responsible name on the package is Frontier Natural Products Co-op Norway, IA.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2387-2015·2015-06-10

    Frontier Organic Vegetarian Brown Gravy Mix Recalled for Salmonella Risk

    Frontier Natural Products Co-op is recalling Simply Organic Vegetarian Brown Gravy Mix packets due to potential Salmonella contamination.

    Product
    Simply Organic Vegetarian Brown Gravy Mix Certified Organic packaged in foil lined paper packet Net Wt. 1.0 OZ. (28 g), UPC 0 89836 18956 1. The product is also marketed under a French/English label Net Wt. 28 g, UPC 0 89836 20007 5. The responsible name on the package is…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1637-2015·2015-06-10

    Synovis Recalls Vascu-Guard Patches Due to Surface Identification Issues

    Synovis is recalling specific Vascu-Guard Peripheral Vascular Patch codes because users reported difficulty distinguishing the smooth from the rough surface.

    Product
    Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and product codes: 1x6cm, product code 1504026, 0.8x8cm, product code 1504028, 1x10cm, product code 1504030, and 2x9cm, product code 1504032. VASCU-GUARD is packaged between two pieces of foam within a double…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2388-2015·2015-06-10

    Frontier Recalls Whole Foods Market Organic Muchi Curry Seasoning Due to Salmonella Risk

    Frontier Natural Products Co-op is recalling Whole Foods Market Organic Muchi Curry Seasoning because the product may be contaminated with Salmonella.

    Product
    Whole Foods Market Organic Muchi Curry Seasoning packaged in a glass bottle, Net Wt 2.08 OZ (59 g), UPC 0 99482 44577 5. The responsible firm name on the label is Whole Foods Market, Austin, TX.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2375-2015·2015-06-10

    Frontier Simply Organic Fish Taco Seasoning Recalled for Salmonella Risk

    Frontier Natural Products Co-op is recalling Simply Organic Fish Taco Seasoning because it may be contaminated with Salmonella. The product was distributed nationwide and to Canada.

    Product
    Simply Organic Fish Taco Seasoning Certified Organic packaged in foil lined paper packet Net Wt. 1.13 OZ. (32 g), UPC 0 89836 18534 1. The responsible name on the package is Frontier Natural Products Co-op Norway, IA.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2365-2015·2015-06-10

    Frontier Natural Products Recalls Organic Fiesta Black Bean Mix Due to Salmonella Risk

    Frontier Natural Products Co-op is recalling specific lots of its Certified Organic Fiesta Black Bean Mix because the product may be contaminated with Salmonella.

    Product
    Frontier Natural Products Co-Op Fiesta Black Bean Mix Certified Organic packaged in a foil packets, Net 453 g 16 oz, UPC 0 89836 02761 0. The responsible name on the package is Frontier Norway, IA.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2404-2015·2015-06-10

    Giant Eagle Recalls Raisin Filled Cookies for Undeclared Milk Allergen

    Giant Eagle is recalling Raisin Filled Cookies sold over the counter because the labels failed to declare the milk allergen. The recall covers products sold in Maryland, Ohio, Pennsylvania, and West Virginia.

    Product
    Raisin Filled Cookie OTC Sell By: (all dates up to) 3/23/2015 Net WT. 1 OZ Contains:Egg, Wheat, Soy ; OTC Raisin Filled Cookie Sell By: (all dates up to) 3/23/2015 Net WT 2 OZ Contains: Egg, Wheat Soy ; Cookies affected are only sold direct from bakery counter and…
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-2386-2015·2015-06-10

    Frontier Simply Organic Creamy Dill Dip Mix Recalled for Salmonella

    Frontier Natural Products Co-op is recalling Simply Organic Creamy Dill Dip Mix due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Simply Organic Creamy Dill Dip Mix Certified Organic packaged in foil lined paper packet Net Wt. 0.70 OZ. (20 g), UPC 0 89836 18843 4. The product is also marketed under a French/English label Net Wt. 24 g, UPC 0 89836 18880 9. The responsible name on the package is Frontier…
    Category
    Food
    Distribution
    Distributed nationwide

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