The Recall Desk

Archive

October 2012 recalls

969 recalls were announced in October 2012.

What the numbers show

Critical
242
Severe
210
High
389
Moderate
113
Low
15

Of the 969 recalls this month scored against our rubric, 25% are Critical, 22% are Severe.

Which agencies issued them

301–400 of 969

  • ModerateFDA (Drugs)·D-014-2013·2012-10-31

    Watson Recalls Lutera Tablets Due to Potential Hydrochlorothiazide Contamination

    Watson Laboratories is recalling specific lots of Lutera tablets because they may contain trace amounts of Hydrochlorothiazide (HCTZ).

    Product
    Lutera (levonorgestrel and ethinyl estradiol) Tablets USP, 0.1 mg/0.02 mg, inert tablets, 28-count tablets per dispenser packaged in 6 Tablet Dispensers per carton, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 92880 USA; Distributed by: Watson Pharma, Inc., Pa
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0134-2013·2012-10-31

    Nipro AquaLiner Hydrophilic Guidewire Recalled for Insufficient Lubricity

    Nipro Medical Corporation is recalling AquaLiner Hydrophilic Guidewires because insufficient lubricity causes them to get stuck in the housing and become nonfunctional.

    Product
    AquaLiner Hydrophilic Guidewire 0.035" X 260cm, Angle/ Regular. AquaLiner Hydrophilic Guidewire is designed for use in angiographic procedures to introduce/ position catheters and interventional devices within the vasculature.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0137-2013·2012-10-31

    Nipro AquaLiner Hydrophilic Guidewires Recalled for Insufficient Lubricity

    Nipro Medical Corporation is recalling AquaLiner Hydrophilic Guidewires because insufficient lubricity causes the wires to get stuck in the housing and become nonfunctional.

    Product
    AquaLiner Hydrophilic Guidewire 0.035" X 260cm, Straight/ Stiff. AquaLiner Hydrophilic Guidewire is designed for use in angiographic procedures to introduce/ position catheters and interventional devices within the vasculature.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0100-2013·2012-10-31

    Westmed Recalls Arterial Blood Gas Kits Due to Contaminated Alcohol Pads

    Westmed is recalling Pulset ABG sampling kits because they contain TRIAD brand alcohol pads that are being recalled for potential contaminants.

    Product
    Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit, Pulset, 3 cc, w/Crickett 22g x 1" A Needle, 25U Balanced Heparin, part number: 3342-95. An arterial blood sampling kit is a device, in kit form, used to obtain arterial blood samples from a patient for blood gas de
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0112-2013·2012-10-31

    Advandx GNR Traffic Light PNA FISH Kit Recalled for False Positives

    Advandx Inc is recalling 187 GNR Traffic Light PNA FISH kits because they may produce false positive results for Pseudomonas putida and Pseudomonas fulva.

    Product
    AdvanDx GNR Traffic Light PNA FISH, In Vitro Diagnostic for Culture Identification Kit for Escherichia coli,and/or Klebsiella pneumoniae and/or Pseudomonas aeruginosa Catalog number: KT011. GNR Traffic Light PNA FISH is a multicolor, qualitative nucleic acid hybridization as
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-010-2013·2012-10-31

    Qualitest Recalls Perphenazine Tablets Due to Cracked Coating

    Vintage Pharmaceuticals is recalling 2,755 bottles of Perphenazine 8 mg tablets due to a possibility of cracked or split tablet coatings.

    Product
    Perphenazine Tablets, USP, 8 mg, 100-count tablets per bottle, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811, NDC 0603-5092-21.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0123-2013·2012-10-31

    Beckman Coulter Recalls DxC 600/800 Analyzers Due to Software Alignment Issue

    Beckman Coulter is recalling 7 UniCel DxC 600/800 analyzers because software v5.0.11 prevents operators from performing a necessary alignment procedure.

    Product
    UniCel¿ DxC 600/800 with Software v5.0.11, Part Number B12218. The UniCel¿ DxC Synchron¿ Clinical Systems are fully automated, computercontrolled clinical chemistry analyzers designed for the in vitro determination of a variety of general chemistries, therapeutic drugs, and o
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0138-2013·2012-10-31

    Nipro AquaLiner Hydrophilic Guidewire Recalled for Insufficient Lubricity

    Nipro Medical Corporation is recalling AquaLiner Hydrophilic Guidewires because insufficient lubricity causes them to get stuck in the housing and become nonfunctional.

    Product
    AquaLiner Hydrophilic Guidewire 0.035" X 180cm, Angle / Regular. AquaLiner Hydrophilic Guidewire is designed for use in angiographic procedures to introduce/ position catheters and interventional devices within the vasculature.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0106-2013·2012-10-31

    Westmed Recalls ABG Sampling Kits Due to Contaminated Alcohol Pads

    Westmed is recalling Pulset ABG sampling kits because they contain TRIAD alcohol pads that may have potential contaminants.

    Product
    Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit, Pulset, 3 cc, 23g x 1" A/B Needle, 25U Balanced Heparin, part numbers: 3373, 3393. An arterial blood sampling kit is a device, in kit form, used to obtain arterial blood samples from a patient for blood gas determinati
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0105-2013·2012-10-31

    Westmed Recalls Arterial Blood Gas Kits Due to Contaminated Alcohol Pads

    Westmed is recalling Pulset ABG sampling kits because they contain TRIAD alcohol pads that may have potential contaminants.

    Product
    Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit, Pulset, 3 cc, w/Crickett 22g x 1" A Needle, 25U Balanced Heparin, part number: 3372-95. An arterial blood sampling kit is a device, in kit form, used to obtain arterial blood samples from a patient for blood gas determ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0024-2013·2012-10-31

    Optovue Recalls Reference Materials Shipped with iVue and RTVue Systems

    Optovue is recalling 795 units of reference materials shipped with iVue and RTVue systems because they were not included in the FDA clearance.

    Product
    Reference materials "RETINAL OCT Analysis and Interpretation Method" shipped with iVue System (K091404) and the "Retina Poster" shipped with iVue System (K091404) and RTVue Systems (K101505); Models: iVue-100, RTVue-100; The physical Product is manufactured and distributed by O
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0101-2013·2012-10-31

    Westmed Recalls Arterial Blood Gas Kits Due to Alcohol Pad Contaminants

    Westmed is recalling ABG sampling kits containing TRIAD alcohol pads due to potential contaminants in the pads.

    Product
    Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit, Pulset, 3 cc, w/Crickett 23g x 1" A Needle, 25U Balanced Heparin, No B Needle or Q-Cork, part number: 3363-95. An arterial blood sampling kit is a device, in kit form, used to obtain arterial blood samples from a p
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0098-2013·2012-10-31

    Westmed Recalls Arterial Blood Gas Kits Due to Alcohol Pad Contaminants

    Westmed is recalling Pulset Arterial Blood Gas sampling kits because they contain TRIAD brand alcohol pads that are being recalled for potential contaminants.

    Product
    Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit, Pulset, 1 cc, 25 g x 5/8" A Needle, 25U Balanced Heparin, part number: 3173-14. An arterial blood sampling kit is a device, in kit form, used to obtain arterial blood samples from a patient for blood gas determinations
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-013-2013·2012-10-31

    Watson Recalls Zovia Tablets Due to Potential Cross-Contamination

    Watson Laboratories is recalling Zovia tablets because certain lots may contain trace amounts of Hydrochlorothiazide (HCTZ) due to cross-contamination.

    Product
    Zovia (ethynodiol diacetate and ethinyl estradiol) Tablets USP, 1 mg/35 mcg, inert tablets, 28-count tablets per dispenser packaged in 6 Tablet Dispensers per carton, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 92880 USA; Distributed by: Watson Pharma, Inc.;
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0122-2013·2012-10-31

    Orthosensor Recalls Knee Trial Software Due to Signal Interference

    Orthosensor is recalling 9 units of Knee Trial software version 1.82 because metal objects in the operating room obstruct the line of sight between the knee balancer and the Link station.

    Product
    "****ORTHO SENSOR**12-123-A Knee Trial for Trithion***1560 Saw grass Corporate Pkwy***4Th floor***Sunrise, FL 33323***www.orthosensor.com***" Rx Only*** Sterile/EO***Made exclusively for Stryker Orthopaedics***. Is the graphic user interface software associated with the grap
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0102-2013·2012-10-31

    Westmed Recalls Arterial Blood Gas Kits Due to Alcohol Pad Contaminants

    Westmed is recalling Pulset ABG sampling kits because they contain TRIAD alcohol pads that are being recalled for potential contaminants.

    Product
    Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit, Pulset, 3 cc, w/Crickett 22g x 1", 25U Balanced Heparin, part number: 3362-95. An arterial blood sampling kit is a device, in kit form, used to obtain arterial blood samples from a patient for blood gas determinations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-015-2013·2012-10-31

    Watson Recalls Zenchent Tablets Due to Potential Hydrochlorothiazide Contamination

    Watson Laboratories is recalling Zenchent tablets because certain lots may be contaminated with trace amounts of Hydrochlorothiazide (HCTZ).

    Product
    Zenchent (norethindrone and ethinyl estradiol) Tablets USP, 0.4 mg/0.035 mg, 28-count tablets per dispenser packaged in 6 Tablet Dispensers per carton, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 92880 USA; Distributed by: Watson Pharma, Inc., Corona, CA 928
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0120-2013·2012-10-31

    Ormco Recalls Damon 3MX Bicuspid Brackets Due to Misidentification

    Ormco/Sybronendo is recalling 148 Damon 3MX Bicuspid Brackets because they were produced with incorrect dark blue ID dots instead of purple, leading to misidentification as maxillary central incisor brackets.

    Product
    The brand name of the device is Damon 3MX Bicuspid Bracket, an orthodontic bracket. Part Number 494-4491, Description -Damon 3MX Bicuspid Bracket, Lot Number - 011265039 Product Usage: Damon 3MX Bicuspid Brackets are intended to be a fixed attachment on a tooth which holds
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-011-2013·2012-10-31

    ABC Compounding Recalls QS Plus Hand Sanitizing Wipes Due to Chemical Contamination

    ABC Compounding Company Inc. is recalling 66 rolls of QS Plus Hand Sanitizing Wipes found to be contaminated with graffiti remover.

    Product
    Earth Force, Ltd., Power Towels, QS Plus Hand Sanitizing Wipes (antiseptic), 50 pre-moistened Wipes, Manufactured by: ABC Compounding Co., Inc., P.O. Box 16247, Atlanta, GA 30321.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0156-2013·2012-10-31

    Baxa Repeater Pump Recall Issued for Contradictory Operator Manual Instructions

    Baxa Corporation is recalling Repeater Pump models 095, 099, and 099R because the included Technical Manual contradicts the Operator Manual regarding multiple source container use.

    Product
    Repeater Pump, Class II device used for facilitating repeatable drug dosage distribution and reconstitution in hospital pharmacies. The device are Fluid Transfer Tube Sets, Sterile/EO, Std Volume Trifurcated, BAXA Corporation, Englewood, CO. The Repeater Pump is a device that
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0110-2013·2012-10-31

    Beckman Coulter Recalls Synchron Multi Calibrator Diskettes Due to Mislabeling

    Beckman Coulter is recalling Synchron Multi Calibrator Diskettes because some units may be mislabeled as Thyroxine (T4) Reagent Calibrator Diskettes.

    Product
    Synchron Systems Synchron Calibrator Multi Calibrator Diskettes, Part Number 442600. The SYNCHRON MULTI-CALIBRATOR, used in conjunction with SYNCHRON reagents, is intended for use on SYNCHRON Systems for the calibration of Albumin, Blood Urea Nitrogen (Urea), Calcium, Choleste
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V518000·2012-10-25

    New Flyer Recalls Transit Buses Due to Parking Brake Fire Risk

    New Flyer is recalling 2010-2012 transit buses because air pressure leaks may cause parking brakes to drag and overheat, potentially resulting in a fire.

    Product
    NEW FLYER — NEW FLYER XDE40, XD35, XDE35, D40LFR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V524000·2012-10-25

    Mitsubishi Fuso Trucks Recalled for Fuel Line Disconnection Risk

    Mitsubishi Fuso is recalling 2012-2013 trucks because a fuel line may disconnect from the filter, potentially causing a fuel leak and fire.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO FEC72, FEC52, FEC92, FGB72
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12E049000·2012-10-25

    Gorilla Automotive Recalls Aftermarket Lug Nuts for Dodge Ram Steel Spares

    Gorilla Automotive Products is recalling aftermarket lug nuts for 2002-2011 Dodge Ram vehicles with steel spare wheels. The nuts may not tighten properly, increasing the risk of the wheel detaching.

    Product
    WHEELS:LUGS/NUTS/BOLTS/STUDS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13703·2012-10-25

    FLO Cycling Recalls Bicycle Wheel Rim Tape Due to Fall Hazard

    FLO Cycling is recalling about 800 units of yellow plastic rim tape sold with specific wheels because the tape can fail, causing inner tubes to burst and posing a fall hazard.

    Product
    Bicycle Wheel Rim Tape
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13020·2012-10-25

    Tricam Recalls Easy Reach Step Stools Due to Fall Hazard

    Tricam Industries is recalling approximately 84,000 Easy Reach step stools sold at The Home Depot because the top step can break, posing a fall hazard.

    Product
    Step Stool
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0134-2013·2012-10-24

    Fresh Tropical Salsa Recalled Due to Potential Salmonella Risk

    Caito Foods Service is recalling Tropical Salsa containing fresh-cut mangoes from Mexico due to potential Salmonella contamination.

    Product
    Garden Highway,Chef Essentials fresh, Tropical Salsa, Net Wt 8 oz, UPC 8.26766-42195.4. Ingredients: Mango, Papaya, Red Onion, Pineapple, Red Bell Pepper, Lime Juice Cilantro, Jalapeno in its Own Juice
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0138-2013·2012-10-24

    FreshLine Recalls Fruit Basket Medley Due to Salmonella Risk

    FreshLine is voluntarily recalling Signature Cafe Fruit Basket Medley containing mangoes from Mexico due to potential Salmonella contamination.

    Product
    Signature Cafe Fruit Basket Medley 30 oz (1 lb 14 oz), UPC 8.26766-06918, Ingredients Grapes,Pineapple, Cantaloupe, Mango, Watermelon, apples
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0147-2013·2012-10-24

    Harry and David Gift Baskets Recalled for Salmonella Contamination

    Harry and David Operations, Inc. is recalling gift baskets containing Daniella brand mangoes due to potential Salmonella contamination.

    Product
    Harry and David and Cushman's Original Gift Baskets
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0129-2013·2012-10-24

    FreshLine Recalls Expired Fruit Burst Products Due to Salmonella Risk

    FreshLine is voluntarily recalling expired Fruit Burst products containing fresh-cut mangoes due to a potential Salmonella risk from a specific Mexican supplier.

    Product
    DeLish, Garden Highway and Generic brands of Fruit Burst, Ingredients: cantaloupe, pineapple, honeydew, watermelon, grapes, strawberries, mango, blueberries packed in its Own Juice; deLISH (Brand), fresh, , Prepared for Walgreen, Inc. Deerfield, IL 60015, 10oz. Generic (B
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0136-2013·2012-10-24

    FreshLine Recalls Expired Fruit Trays Containing Mangoes Due to Salmonella Risk

    FreshLine is voluntarily recalling expired fruit trays containing mangoes from Mexico due to potential Salmonella contamination.

    Product
    Fruit Tray, Generic Label Sold at Wal-Mart Stores, 1 lb 14 oz, UPC 8.26766-25588.7. Ingredients Pineapple, Apples,{ Apples calcium ascorbate (a blend of calcium and vitamins to maintain color)}, Cantaloupe, Mango, Grapes
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0125-2013·2012-10-24

    Evolution Fresh Cinnamon Apple Almond Butter Sandwiches Recalled for Salmonella

    Gretchen's Shoebox Express is recalling Evolution Fresh Cinnamon and Apple Almond Butter Sandwiches because the almond butter may be contaminated with Salmonella.

    Product
    Evolution Fresh brand Cinnamon and Apple Almond Butter Sandwiches in plastic wrap, NET WT 5.75 oz., UPC 726111926371. Label reads in part, perishable. keep refrigerated. CINNAMON APPLE & ALMOND BUTTER SANDWICH; MANUFACTURED FOR EVOLUTION FRESH, INC.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0110-2013·2012-10-24

    Whole Foods Recalls Ricotta Salata Cheese Due to Listeria Risk

    Whole Foods Market is recalling Frescolina and Mitica Ricotta Salata cheeses in 21 states and D.C. because they may be contaminated with Listeria monocytogenes.

    Product
    Frescolina and Mitica brand Ricotta Salata cheeses were cut into wedges, packaged in clear plastic wrap and sold with a Whole Foods Market scale label using PLU 293427 and PLU 294413, respectively. All "sell by" dates through Oct. 2 are affected.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0141-2013·2012-10-24

    Kilwin's Sugar Free Peanut Butter Fudge Recalled for Salmonella Risk

    Kilwin's is recalling Sugar Free Peanut Butter Fudge because the peanut butter ingredient is associated with a Sunland, Inc. recall and may be contaminated with Salmonella.

    Product
    Kilwins Sugar Free S/F PEANUT BUTTER FUDGE, Nt. Wt. 7-oz (198 g)
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-2395-2012·2012-10-24

    Splendid Products Recalls Daniella Mangoes Due to Salmonella Contamination Risk

    Splendid Products is recalling Daniella brand mangoes because they may be contaminated with Salmonella. The fruit is linked to recent salmonellosis cases in Canada and possibly the US.

    Product
    Daniella Mangoes May be identified by Daniella sticker with a PLU code of 3114, 4051, 4311, 4584 or 4959.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0130-2013·2012-10-24

    FreshLine Recalls deLISH Mango and Berry Mix Due to Salmonella Risk

    FreshLine is voluntarily recalling deLISH Mango & Berry Mix prepared for Walgreens because the mangoes may contain Salmonella.

    Product
    deLISH, fresh, Mango & Berry Mix, 10oz., UPC 0.49022-63779.5, Prepared for Walgreen, Inc. Deerfield, IL 60015, Ingredients: Mango, strawberries, blueberries packed in its Own Juice.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0291-2013·2012-10-24

    Late July Organic Mini Peanut Butter Sandwich Crackers Recalled for Salmonella Risk

    Late July Snacks is recalling Organic Mini Peanut Butter Sandwich Crackers due to potential Salmonella contamination from Sunland peanut butter.

    Product
    Late July Organic Mini Peanut Butter Sandwich Crackers packaged in : 5oz box UPC 890444000700 8ct carton/1.125oz (single serve caddy) & 1.125oz pack (single serve pack UPC: 890444000724 & 890444000717
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0108-2013·2012-10-24

    Publix Chopped Hearts of Romaine Recalled for Listeria Monocytogenes

    Publix Super Markets is recalling Chopped Hearts of Romaine due to the presence of Listeria monocytogenes confirmed by the FDA.

    Product
    ***Publix***Hearts of Romaine***Chopped Hearts of Romaine***Triple Washed***& Ready to Eat***No Preservatives***NET WT 10 OZ (284g)***
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0132-2013·2012-10-24

    FreshLine Recalls Tropical Fruit Medley Due to Salmonella Risk

    FreshLine is voluntarily recalling Tropical Fruit Medley products containing fresh-cut mangoes due to a potential Salmonella risk associated with mangoes from Mexico.

    Product
    Tropical Fruit Medley, Ingredients Pineapple, Mango & Papaya; Garden Highway ( brand) Net Wt 1 lb, UPC 8.26766-26848.1 Trader Joe's, Nt. Wt. 16 oz (1 lb) 454 g, UPC 00949361 deLISH (brand) Nt. Wt. 10 oz.(285g), UPC 49022 53699
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0144-2013·2012-10-24

    Cushman's Fruit and Flower Basket Recalled for Salmonella Risk

    Harry and David Operations, Inc. is recalling Cushman's Fruit and Flower Baskets due to potential Salmonella contamination from mangoes used in the product.

    Product
    Cushman's Fruit and Flower Basket
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0148-2013·2012-10-24

    World Food LLC Recalls Fresh Fruit Burst Cups Due to Salmonella Risk

    World Food LLC is recalling Fresh Fruit Burst fruit cups because they may contain mangoes contaminated with Salmonella. The product was distributed throughout Florida.

    Product
    Fresh Fruit Burst fruit cup, packaged in 1 and 1.5 lb containers. Labeled in part: "***Fruit Burst***Ingredients: Watermelon, Cantaloupe, Pineapple, Honeydew, Grapes, Mango, Blueberries. Packed in its own juice***"
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0139-2013·2012-10-24

    Starbuck Protein Bistro Box Recalled for Potential Salmonella Contamination

    Gretchen's Shoebox Express is recalling Starbuck Protein Bistro Boxes because the included Honey Peanut Butter squeeze packs may contain peanut contaminated with Salmonella.

    Product
    Starbuck Protein Bistro Box, 6.80 oz. package, UPC 762111881502. The Starbuck Protein Bistro Box contains the 0.5 oz. single-serve Honey Peanut Butter Blend squeeze pack with the UPC 894455000391.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0292-2013·2012-10-24

    Newman's Own Peanut Butter Cookies Recalled for Salmonella Risk

    Newman's Own Organics is recalling Newman-O's Peanut Butter Creme Filled Chocolate Cookies because they were made with peanut butter that may be contaminated with Salmonella.

    Product
    Newman's Own Organics brand Newman-O's Peanut Butter Creme Filled Chocolate Cookies 8oz/6 pack, Unit UPC#7 57645 02170 8, Case UPC#7 57645 02171 5; 13oz/6 pack, Unit UPC# 7 57645 02150 0, Case UPC#7 57645 02151 7; 9oz/6 pack, Unit UPC#7 57645 02288 0, Case UPC # 7 57645
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0126-2013·2012-10-24

    Evolution Fresh Almond Butter Recalled for Potential Salmonella Contamination

    Gretchen's Shoebox Express is recalling Evolution Fresh brand Almond Butter in 2-oz containers because the almond butter supplied by Sunland, Inc. is potentially contaminated with Salmonella.

    Product
    Evolution Fresh brand Almond Butter in individual 2-oz containers, UPC 726111926838. Label reads in part, perishable. keep refrigerated. ALMOND BUTTER, NET WT 2 OZ, MANUFACTURED FOR EVOLUTION FRESH, INC.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0128-2013·2012-10-24

    FreshLine Recalls Fresh-Cut Mango Products Due to Salmonella Risk

    FreshLine is voluntarily recalling expired fresh-cut mango products prepared for Walgreens due to a potential Salmonella risk from mangoes sourced from Mexico.

    Product
    deLISH, fresh, Pineapple, mango, & cantaloupe spears ( 5 oz), UPC 0.49022-53701.9 and tropical medley, (10 oz), UPC 0.49022-53699.9. Prepared for Walgreen, Inc. Deerfield, IL 60015. Ingredients: Cantaloupe, Mango, Pineapple, Packed in its Own Juice, Grown In USA, Mexico, Costa R
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0150-2013·2012-10-24

    World Foods Recalls Fresh Island Medley for Potential Salmonella Contamination

    World Foods, LLC is recalling Fresh Island Medley fruit containers due to potential Salmonella contamination from mangoes supplied by Agricola Daniella.

    Product
    Fresh Island Medley, packaged in 1 lb containers. Labeled in part: "***Island Medley***Ingredients: Pineapple, Mango, Papaya***Packed in its own juice****"
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0251-2013·2012-10-24

    Spartan Central Kitchen Recalls Macaroni Salad Due to Listeria Contamination

    Spartan Central Kitchen is voluntarily recalling 5-pound cans of #309 Macaroni Salad manufactured between August 20 and September 10, 2012, due to possible Listeria contamination.

    Product
    #309 Macaroni Salad, Old Fashioned 309 5 pounds
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0173-2013·2012-10-24

    Spartan Central Kitchen Recalls Broccoli Au Gratin Due to Listeria Risk

    Spartan Central Kitchen is voluntarily recalling 10-ounce Broccoli Au Gratin products manufactured in August and September 2012 due to possible Listeria contamination found during an FDA inspection.

    Product
    #460 10 oz Broccoli Augratin 10 ounces
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0114-2013·2012-10-24

    Sunshine Peanut Company Recalls Peanut Butter for Aflatoxin Contamination

    Sunshine Peanut Company is recalling specific lots of peanut butter because routine USDA sampling found aflatoxin levels exceeding 20 ppb.

    Product
    Sunny Boy Low Sodium/ Low Salt Peanut Butter. Product is labeled in part: 35 lb pail labeled in part: ""SunnyBoy LowSodium/LowSalt***PEANUT BUTTER***Net Wt. 35lb. (15.89 KG)***INGREDIENTS: Peanuts, Dextrose, Contains less than 2% of the following: Partially Hydrogenated Oil (
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0117-2013·2012-10-24

    Sunshine Peanut Company Recalls Peanut Butter Due to Aflatoxin Levels

    Sunshine Peanut Company is recalling specific lots of peanut butter because routine USDA sampling found aflatoxin levels exceeding 20 ppb.

    Product
    Product is 2 oz Peanut Butter. 2 oz pouch labeled in part: "PEANUT BUTTER 2 oz. Pouch***Ingredients: Roaster Peanuts, Sugar, Hydrogenated Vegetable Oil, (Rapeseed Cottonseed and/or Soybean Oils), Salt.***Allergen Warning: Contains Peanuts***Sunshine Peanut Company Jacksonville,
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0116-2013·2012-10-24

    Sunshine Peanut Company Recalls Peanut Butter Due to Aflatoxin Levels

    Sunshine Peanut Company is recalling specific lots of peanut butter because routine USDA sampling found aflatoxin levels exceeding 20 ppb.

    Product
    Product is 1 oz Peanut Butter. 1 oz pouch labeled in part: "PEANUT BUTTER***Ingredients: Roaster Peanuts, Sugar, Stabilizer (Rapeseed Cottonseed and/or Soybean Oils), Salt.***Allergen Warning: Contains Peanuts***Sunshine Peanut Company Jacksonville, FL 32204***SP767***" Case
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0135-2013·2012-10-24

    FreshLine Recalls Expired Watermelon Mango Medley Due to Salmonella Risk

    FreshLine is voluntarily recalling expired Garden Highway Watermelon Mango Medley products due to a potential Salmonella risk associated with mangoes from Mexico.

    Product
    Garden Highway,Watermelon Mango Medley, Net Wt 7oz, UPC 8.26766-24062.3, Ingredients: Watermelon, Mango, Blueberries in its Own Juice
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0149-2013·2012-10-24

    World Foods Recalls Mango Spears for Potential Salmonella Contamination

    World Foods, LLC is recalling 1 lb containers of Mango Spears due to potential Salmonella contamination from a supplier.

    Product
    Mango Spears, packaged in 1 lb containers. Labeled in part: "***Mango Spears***Ingredients: Mango***Packed in its own juice***Grown in: Mexico ***"
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0124-2013·2012-10-24

    Specialty Commodities Recalls Raw Macadamia Nuts for Salmonella Risk

    Specialty Commodities, Inc. is recalling raw, shelled macadamia nuts due to potential Salmonella contamination. The affected product was distributed to seven states.

    Product
    Macadamia Nuts Style 2, RAW, SHELLED. DESCRIPTION OF CARTON FROM GUATEMALA: LOT 2 70 JUNE 25/12 423, 43 1 NORMAL/BIG .
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-0133-2013·2012-10-24

    FreshLine Recalls Mango Salsa Due to Salmonella Risk

    FreshLine is voluntarily recalling Garden Highway Chef Essentials Mango Salsa because the fresh-cut mangoes may contain Salmonella.

    Product
    Garden Highway, Chef Essentials, Mango Salsa, Net Wt 7 oz, UPC 8.26766-42208.1, Ingredients: Mango, Lime Juice, Red Onion, Mint, Jalapeno Pepper, Packed in It's Own Juice
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0248-2013·2012-10-24

    Spartan Central Kitchen Recalls Seafood Pasta Salad Due to Listeria Risk

    Spartan Central Kitchen is voluntarily recalling 5-pound Seafood Pasta Salad products manufactured between August 20 and September 10, 2012, due to possible Listeria contamination.

    Product
    #312 Seafood Pasta Salad 312 5 pounds
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0122-2013·2012-10-24

    Frescolina Ricotta Salata Cheese Recalled for Listeria Contamination

    Floyd Peterson Company Inc. is recalling Frescolina Ricotta Salata cheese due to potential Listeria monocytogenes contamination.

    Product
    Ricotta Salata Frescolina Brand Soft Cheese. Product is packaged in a retail package, wedge shaped, size ranges from 6-7 oz. The product is labeled in parts: "***Frescolina Ricotta Salata MARTE***IMPORTED BY FOREVER CHEESE,NY 11106***PRODUCT OF ITALY***"
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0146-2013·2012-10-24

    Harry and David Fresh Fruit Gift Baskets Recalled for Salmonella

    Harry and David is recalling Fresh Fruit Gift Baskets and Deluxe varieties due to potential Salmonella contamination from mangoes.

    Product
    Harry and David Fresh Fruit Gift Basket and Fresh Fruit Gift Basket Deluxe
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0137-2013·2012-10-24

    FreshLine Recalls Seasonal Blend Fresh Fruit Due to Salmonella Risk

    FreshLine is recalling Seasonal Blend Fresh Fruit containing mangoes from Mexico due to potential Salmonella contamination.

    Product
    Seasonal Blend Fresh Fruit, 16 oz (1 lb), UPC 8.26766-25534.4 and 32 oz (2 lb), UPC 8.26766.26805.4.Generic Label Sold at Wal-Mart Stores Ingredients Pineapple, Cantaloupe, Honeydew, Strawberries, Grapes, Mango
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0189-2013·2012-10-24

    Spartan Central Kitchen Recalls Italian Sausage Penne Due to Listeria Risk

    Spartan Central Kitchen is voluntarily recalling 10 oz Italian Sausage Penne products manufactured in August and September 2012 due to possible Listeria contamination found during an FDA inspection.

    Product
    #436 10 oz Italian Sausage Penne 10 ounces
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0286-2013·2012-10-24

    Spartan Central Kitchen Recalls Peppers and Onions for Listeria Risk

    Spartan Central Kitchen is voluntarily recalling 0.75-pound packages of Red-Yellow-Green Peppers and Onions due to possible Listeria contamination found during an FDA inspection.

    Product
    #008 Red-Yellow-Green Peppers, Onions 0.75 pounds
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0127-2013·2012-10-24

    FreshLine Recalls Expired Fresh-Cut Mangoes Due to Salmonella Risk

    FreshLine is voluntarily recalling expired fresh-cut mangoes from Mexico due to a potential Salmonella risk.

    Product
    Nice, Fruit Mango, Product of Mexico, single, 6 ct; UPC 0.4902252988.5
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0131-2013·2012-10-24

    FreshLine Recalls Fresh-Cut Mango Spears Due to Salmonella Risk

    FreshLine is voluntarily recalling fresh-cut mango spears due to a potential Salmonella risk associated with mangoes from a specific Mexican supplier.

    Product
    Garden Highway, fresh, Mango spears, packed in its Own Juice, Grown In: Mexico Net Wt 1 lb (454g), 1.5 lbs(680 g); 2 lbs (32 oz); Delish Mango Spears (5 oz, 1 lb) for Walgreens ; Generic Label Mango Spears for Kroger (1 lb)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0244-2013·2012-10-24

    Spartan Central Kitchen Recalls Cherry Chicken Penne Salad Due to Listeria

    Spartan Central Kitchen is voluntarily recalling Cherry Chicken Penne Salad manufactured between August 20 and September 10, 2012, due to possible Listeria contamination found during an FDA inspection.

    Product
    #319 Cherry Chicken Penne Salad 319 5 pounds
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0111-2013·2012-10-24

    Carol's Cuts Cubed Mangos Recalled Due to Salmonella Contamination

    Liberty Fruit Co Inc is recalling 185 trays of Carol's Cuts cubed mangos potentially contaminated with Salmonella gaminara. The product was distributed in Kansas.

    Product
    Carol's Cuts, mangos cubed, item # 71035, packaged in 5-lb, black plastic tray, heat sealed with a film lid, single-use package. The responsible firm name on the label is Carol's Cuts, Kansas City, KS
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0120-2013·2012-10-24

    Lehi Valley Trading Co. Recalls Licorice Sticks Due to Lead Levels

    Lehi Valley Trading Co. is voluntarily recalling various brands of licorice sticks because testing found lead levels above FDA limits.

    Product
    Licorice Sticks sold under the following brand names: 1) Orange Patch Country Store Licorice Sticks, New Wt, 12 oz. Packaged in plastic bag; 2) Desert Delite Licorice Sticks, New Wt, 12 oz. Packaged in plastic bag; 3) 17th Street Market Licorice Sticks, New Wt, 12 oz. Package
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0094-2013·2012-10-24

    Osteotech Recalls Grafton and Xpanse Bone Graft Products Due to Sterility Concerns

    Osteotech Inc is recalling multiple lots of Grafton and Xpanse bone graft products because the sterility of the inner pouch surface may be compromised.

    Product
    Optimum Expanse S Multiple sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0056-2013·2012-10-24

    Beckman Coulter AutoMate 1250 and 2550 Sample Processing System Recall

    Beckman Coulter is recalling AutoMate 1250 and 2550 systems due to a risk of sample misidentification caused by duplicate barcode labels.

    Product
    AutoMate 1250 and AutoMate 2550, Part Numbers ODL25125 and ODL25255. The AutoMate 1200/2500 System Series is a semi-open, pre- and post-analytical sample processing and sorting system. The base system automates the sample sorting, decapping, and archiving processes. Handling a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0160-2013·2012-10-24

    Spartan Central Kitchen Recalls Garden Fresh Salads for Listeria Risk

    Spartan Central Kitchen is voluntarily recalling Garden Fresh salads due to possible Listeria contamination found during an FDA inspection.

    Product
    #762 Salad - Large Garden Fresh 3/4 pounds #761 Salad - Small Garden Fresh 3 oz.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0072-2013·2012-10-24

    MOOG Medical Devices Recalls Curlin Infusion Administration Sets

    MOOG Medical Devices Group is recalling 12,000 Curlin Infusion Administration Sets due to an incomplete previous recall regarding unclearable Air-In-Line alarms.

    Product
    ***This recall is being conducted due to an incomplete recall for RES 57829*** Curlin Infusion Administration Set, REF 340-4165, Sterile EO, The Curlin Ambulatory Infusion Pump System with disposable PVC Administration Tubing Sets and user accessories, provide a means for th
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·12V517000·2012-10-24

    Altec Recalls 2011-2012 CFD 1217 Wood Chippers Due to Blade Defect

    Altec is recalling 2011-2012 CFD 1217 wood chippers because blades may not meet hardness specifications, posing a risk of injury if they fail.

    Product
    ALTEC — ALTEC CFD 1217 WOOD CHIPPER
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0089-2013·2012-10-24

    Osteotech Recalls Grafton and Xpanse Bone Graft Products Due to Sterility Concerns

    Osteotech Inc is recalling multiple lots of Grafton and Xpanse bone graft products because the sterility of the inner pouch surface may be compromised.

    Product
    Grafton DBM Matrix Strips Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0078-2013·2012-10-24

    Teleflex Recalls Hem-o-lok Polymer Clips Due to Sterility Concerns

    Teleflex Medical is recalling 126 units of Hem-o-lok Large Polymer Ligating Clips because pinholes in the trays may compromise sterility.

    Product
    Hem-o-lok Large Polymer Ligating Clips, REF #544240, Rx only, Sterile, Teleflex Medical, Research Triangle Park, NC 27709. Teleflex Medicals Hem-o-lok polymer ligating clips are single use, sterile, non-absorbable medial devices that have been designed to ligate vessels and t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0159-2013·2012-10-24

    Spartan Central Kitchen Recalls Chef Salads Due to Listeria Contamination

    Spartan Central Kitchen is voluntarily recalling Large and Small Chef Salads manufactured in August and September 2012 due to possible Listeria contamination found during an FDA inspection.

    Product
    #764 Salad - Large Chef 3/4 pounds #763 Salad - Small Chef 1/4 pound
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0064-2013·2012-10-24

    ConMed Linvatec Recalls PressFT Sutures Due to Driver Tip Separation Risk

    ConMed Linvatec is recalling PressFT HI-FI Sutures because the driver tip may separate from the shaft after implant insertion.

    Product
    "***PressFT***2.6 w/ One #2 (5 metric) Hi-Fi***Suture***NP261***2009-02***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA*** To reattach soft tissue to bone in orthopedic surgical procedures
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Food)·F-0277-2013·2012-10-24

    Spartan Central Kitchen Recalls Diced Colored Peppers Due to Listeria Risk

    Spartan Central Kitchen is voluntarily recalling 9-ounce cans of diced colored peppers manufactured between August 20 and September 10, 2012, due to possible Listeria contamination.

    Product
    #025 Diced Colored Peppers 9 ounces
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0083-2013·2012-10-24

    Osteotech Recalls Grafton and Xpans Bone Graft Products Due to Sterility Concerns

    Osteotech is recalling multiple lots of Grafton and Xpans bone graft products because the sterility of the inner pouch surface may be compromised.

    Product
    Grafton DBM Putty Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0215-2013·2012-10-24

    Spartan Central Kitchen Recalls Egg Spread Due to Listeria Contamination

    Spartan Central Kitchen is voluntarily recalling 5-pound #357 Egg Spread products manufactured in August and September 2012 due to possible Listeria contamination found during an FDA inspection.

    Product
    #357 Egg Spread 5 pounds
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0279-2013·2012-10-24

    Spartan Central Kitchen Recalls Soup Starter Due to Listeria Contamination

    Spartan Central Kitchen is voluntarily recalling 8-ounce Soup Starter products manufactured in August and September 2012 due to possible Listeria contamination found during an FDA inspection.

    Product
    #023 Soup Starter 8 ounces
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0276-2013·2012-10-24

    Spartan Central Kitchen Recalls Diced Onions for Listeria Contamination

    Spartan Central Kitchen is voluntarily recalling diced white and red onions due to possible Listeria contamination found during an FDA inspection.

    Product
    #027 Diced White Onions 6 ounces and #026 Diced Red Onions 6 ounces
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0179-2013·2012-10-24

    Spartan Central Kitchen Recalls Three Green Veggies for Listeria Risk

    Spartan Central Kitchen is voluntarily recalling 10-ounce Three Green Veggies products due to possible Listeria contamination found during an FDA inspection.

    Product
    #448 10 oz Three Green Veggies 10 ounces
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0088-2013·2012-10-24

    Osteotech Recalls Grafton and Xpansé Bone Graft Products Due to Sterility Concerns

    Osteotech is recalling multiple lots of Grafton and Xpansé bone graft products because the sterility of the inner pouch surface may be compromised.

    Product
    Grafton DBM Matrix PLF Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0085-2013·2012-10-24

    Osteotech Recalls Grafton and Xpans Bone Graft Products Due to Sterility Concerns

    Osteotech is recalling multiple lots of Grafton and Xpans bone graft products because the sterility of the inner pouch surface may be compromised.

    Product
    Grafton DBM Flex Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone graft substitute and b
    Category
    Medical Device
    Distribution
    Distributed nationwide

Looking for a different month? Back to 2012.