The Recall Desk

Archive

November 2012 recalls

569 recalls were announced in November 2012.

What the numbers show

Critical
111
Severe
99
High
164
Moderate
162
Low
33

Of the 569 recalls this month scored against our rubric, 20% are Critical, 17% are Severe.

401–500 of 569

  • ModerateFDA (Devices)·Z-0249-2013·2012-11-14

    Zimmer MS-30 Sterile Shafts Recalled for Labeling Discrepancies

    Zimmer Inc. is correcting patient labels for MS-30 Sterile Shafts due to discrepancies in reference and lot numbers.

    Product
    MS-30 Shaft, Sterile, Rx
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0207-2013·2012-11-14

    OrthoPediatrics Recalls Trochar Scalpel Instruments for Design Defect

    OrthoPediatrics Corp is recalling 78 trochar scalpel instruments that were not manufactured to design specifications and will not function as intended.

    Product
    Trochar Scalpel Instrument (Surgical Punch) OrthoPediatrics intramedullary rods (nails) are generally rod-shaped devices, with screw holes at either end for fixation to bone. This device is intended to be inserted into the medullary canal of the femur for fixation of fractures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0228-2013·2012-11-14

    Zimmer Inverse/Reverse Screw System Label Correction

    Zimmer, Inc. is correcting patient labels for Inverse/Reverse Screw systems manufactured before March 2010 due to discrepancies in reference and lot numbers.

    Product
    Zimmer Inverse/Reverse Screw system,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0254-2013·2012-11-14

    Sysmex XE-2100 Hematology System Recalled for Reticulocyte Count Bias

    Sysmex America is recalling 1,099 XE-2100 Automated Hematology Systems because reticulocyte counts may be 21% lower than expected due to a low bias.

    Product
    Sysmex XE-2100 Automated Hematology System; an automated differential cell counter; Sysmex Corporation, Kobe, Japan; Sysmex America, One Nelson C. White Parkway, Mundelein, IL 60060; catalog #983-1341-1 The Sysmex XE-2100 is an automated hematology analyzer for in vitro dia
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0232-2013·2012-11-14

    Zimmer Anatomical Shoulder Ball Taper Label Correction

    Zimmer Inc. is correcting patient labels for Anatomical Shoulder Ball Tapers due to discrepancies in reference and lot numbers.

    Product
    Anatomical Shoulder" Ball taper for humeral stem
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0642-2013·2012-11-14

    Penn State Creamery Recalls Ice Cream Due to Plastic Foreign Objects

    Penn State Creamery is voluntarily recalling specific ice cream and frozen yogurt products due to reports of small plastic foreign objects.

    Product
    Penn State Creamery/Berkey Creamery Ice Cream -- Keeny Beany Chocolate flavor; 3 gallon (paper), 1/2 gallon (paper) and pints (plastic)
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0263-2013·2012-11-14

    Shimadzu Recalls Mobile X-ray Systems for Beam Quality Non-Compliance

    Shimadzu Medical Systems is recalling 133 mobile X-ray systems because certain units may not meet federal beam quality standards.

    Product
    0.7/1.3U163CS-36 In combination with below systems MobileArt Evolution, MobileDaRt Evolution Product Usage: The device is a mobile X-ray system in order to take general radiography of patients in the hospital who cannot move and/or of outpatients in emergency.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0643-2013·2012-11-14

    Penn State Creamery Recalls German Chocolate Cake Ice Cream

    Penn State Creamery is voluntarily recalling German Chocolate Cake ice cream due to reports of small plastic foreign objects in the product.

    Product
    Penn State Creamery/Berkey Creamery Ice Cream -- German Chocolate Cake flavor; 3 gallon (paper), 1/2 gallon (paper) and pints (plastic)
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0230-2013·2012-11-14

    Zimmer Recalls Anatomical Shoulder Implants Due to Labeling Discrepancies

    Zimmer Inc. is correcting patient labels for 228 anatomical shoulder implants manufactured before March 2010 due to reported discrepancies between product and patient labels.

    Product
    Anatomical Shoulder" Inverse/Reverse Glenoid Sterile, Rx
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0649-2013·2012-11-14

    Penn State Creamery Recalls Frozen Yogurt Due to Plastic Foreign Objects

    Penn State Creamery is voluntarily recalling vanilla frozen yogurt due to reports of small plastic foreign objects in the product.

    Product
    Penn State Creamery/Berkey Creamery Frozen Yogurt - Vanilla flavor; 3 gallon (paper), 1/2 gallon (paper) and pints (plastic)
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0650-2013·2012-11-14

    Penn State Creamery Recalls Strawberry Frozen Yogurt Due to Plastic Foreign Objects

    Penn State Creamery is voluntarily recalling strawberry frozen yogurt due to reports of small plastic foreign objects in the product.

    Product
    Penn State Creamery/Berkey Creamery Frozen Yogurt - Strawberry flavor; 3 gallon (paper), 1/2 gallon (paper), and pints (plastic)
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0256-2013·2012-11-14

    Sysmex XE-2100C Hematology System Recalled for Reticulocyte Count Bias

    Sysmex America is recalling 69 XE-2100C automated hematology systems because reticulocyte counts may be 21% lower than expected.

    Product
    Sysmex XE-2100C Automated Hematology System; an automated differential cell counter; Sysmex Corporation, Kobe, Japan; Sysmex America, One Nelson C. White Parkway, Mundelein, IL 60060; catalog #053-2311-4 The Sysmex XE-2100C is an automated hematology analyzer for in vitro dia
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0193-2013·2012-11-14

    Clinical Diagnostic Solutions Recalls Boule Con Diff US Tri Pack Hematology Controls

    Clinical Diagnostic Solutions is recalling Boule Con Diff US Tri Pack hematology controls due to customer reports of inaccurate MCV and RDW% values.

    Product
    Boule Con Diff US Tri Pack, 6 Vials. For in vitro diagnostic use as a control to monitor the performance of multi-parameter hematology instruments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0231-2013·2012-11-14

    Zimmer Recalls Shoulder Humeral Inserts Due to Label Discrepancies

    Zimmer Inc. is correcting patient labels for 74 anatomical shoulder humeral inserts manufactured before March 2010 due to reported discrepancies in reference and lot numbers.

    Product
    Anatomical Shoulder" Inverse/Reverse Humeral PE-Insert Sterile, Rx
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0217-2013·2012-11-14

    Zimmer MS-30 Stem Recall for Patient Label Discrepancies

    Zimmer Inc. is correcting patient labels for MS-30 Stems manufactured before March 2010 due to discrepancies in reference and lot numbers.

    Product
    MS-30¿ Stem
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0221-2013·2012-11-14

    Zimmer Recalls Wagner Cone Prostheses Due to Label Discrepancies

    Zimmer Inc. is correcting patient labels for Wagner cone prostheses manufactured before March 2010 due to discrepancies in reference and lot numbers.

    Product
    Wagner cone Prosthesis, uncemented, sterile, Rx
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0253-2013·2012-11-14

    Siemens Dimension Vista Homocysteine Reagent Cartridges Recalled for Leaking

    Siemens Healthcare Diagnostics is recalling 583 cartons of Dimension Vista Homocysteine Reagent Cartridges because they are leaking from their wrappers.

    Product
    Siemens Dimension Vista(R) Homocysteine Flex(R) Reagent Cartridge This is an in vitro diagnostic test for the quantitative measurement of total homocysteine (HCYS) in human serum, heparinized plasma, and EDTA plasma on the Dimension Vista(R) System. Measurements of homocystein
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0224-2013·2012-11-14

    Zimmer Recalls Anatomical Shoulder Fracture Humeral Stems for Label Discrepancies

    Zimmer, Inc. is correcting patient labels for 139 Anatomical Shoulder Fracture Humeral stems due to discrepancies between product and patient labels regarding reference and lot numbers.

    Product
    Anatomical Shoulder" Fracture Humeral stem
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-046-2013·2012-11-14

    Valeant Recalls AcneFree Toner Pads Due to Low Salicylic Acid Content

    Valeant Pharmaceuticals is recalling AcneFree Acne Astringent Toner Pads because the salicylic acid ingredient was found to be subpotent.

    Product
    AcneFree Acne Astringent Toner Pads (salicylic acid 2% w/v); 60-count pads per jar, Dist. by: University Medical Pharmaceuticals Corp., Irvine, CA 92618, UPC 7 88521 13551 6.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0223-2013·2012-11-14

    Zimmer Anatomical Shoulder Humeral Stem Label Correction

    Zimmer Inc. is correcting patient labels for Anatomical Shoulder Humeral stems due to discrepancies in reference and lot numbers.

    Product
    Anatomical Shoulder" Humeral stem
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0243-2013·2012-11-14

    Zimmer NCB Cancellous Screw Label Correction Recall

    Zimmer Inc. is correcting patient labels for NCB cancellous screws due to discrepancies in reference and lot numbers.

    Product
    NCB¿ cancellous screw
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-047-2013·2012-11-14

    Valeant Recalls Subpotent AcneFree 3-in-1 Acne Night Repair Foam

    Valeant Pharmaceuticals is recalling AcneFree 3-in-1 Acne Night Repair Foam because the salicylic acid ingredient is subpotent and the label is inaccurate.

    Product
    AcneFree 3-in-1 Acne Night Repair Foam (retinol + salicylic acid 1.5% w/v), 3 oz (85 g) canister, Dist. by: University Medical Pharmaceuticals Corp., Irvine, CA 92618, UPC 7 88521 13548 6.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0192-2013·2012-11-14

    Abbott Recalls Cliniqa Liquid QC Cardiac Marker Control for i-STAT

    Abbott Point of Care is recalling specific lots of Cliniqa Liquid QC Cardiac Marker Control for i-STAT because results may be generated below the lower value assignment range.

    Product
    Cliniqa Liquid QCTM Cardiac Marker Control for i-STAT Level 1 (List Number 06F12-09; Lot Number 071039) Cliniqa Liquid QCTM Cardiac Marker Control for i-STAT Level 2 (List Number 06F12-10; Lot Number 081039) Cliniqa Liquid QCTM Cardiac Marker Control for i-STAT Level 3 (Lis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0225-2013·2012-11-14

    Zimmer Anatomical Shoulder Humeral Head Label Correction

    Zimmer, Inc. is correcting patient labels for Anatomical Shoulder Humeral Heads manufactured before March 2010 due to discrepancies in reference and lot numbers.

    Product
    Anatomical Shoulder" Humeral Head
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0194-2013·2012-11-14

    Clinical Diagnostic Solutions Recalls Boule Con-Diff Hematology Control Vials

    Clinical Diagnostic Solutions is recalling Boule Con-Diff hematology control vials because customers reported inaccurate MCV and RDW% values.

    Product
    Boule Con-Diff Hematology Control 9 vials. For in vitro diagnostic use as a control to monitor the performance of multi-parameter hematology instruments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0190-2013·2012-11-14

    Clinical Diagnostic Solutions Recalls Boule Con-Diff Hematology Control Vials

    Clinical Diagnostic Solutions is recalling Boule Con-Diff hematology control vials due to a received complaint. The product is used to monitor multi-parameter hematology instruments.

    Product
    Boule Con-Diff Hematology Control For in vitro diagnostic use as a control to monitor the performance of multi-parameter hematology instruments.
    Category
    Medical Device
    Distribution
    31 states
  • LowFDA (Devices)·Z-0242-2013·2012-11-14

    Zimmer Recalls Dynesys Pedicle Screws Due to Labeling Discrepancies

    Zimmer Inc. is correcting patient labels for Dynesys Top-Loading System Cannulated Pedicle + Set Screws manufactured before March 2010 due to discrepancies between product and patient labels.

    Product
    Dynesys¿ Top-Loading System Cannulated Pedicle + Set Screw
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0191-2013·2012-11-14

    Clinical Diagnostic Solutions Recalls Boule Con-Diff Hematology Control Vials

    Clinical Diagnostic Solutions is recalling Boule Con-Diff hematology control vials due to a received complaint. The product is used to monitor multi-parameter hematology instruments.

    Product
    Boule Con-Diff Hematology Control For in vitro diagnostic use as a control to monitor the performance of multi-parameter hematology instruments.
    Category
    Medical Device
    Distribution
    31 states
  • LowFDA (Devices)·Z-0215-2013·2012-11-14

    Zimmer Recalls Metasul LDH Head Due to Patient Label Discrepancies

    Zimmer, Inc. is correcting patient labels for Metasul LDH Head Rx Sterile products manufactured before March 2010 due to discrepancies in reference and lot numbers.

    Product
    Metasul¿ LDH¿ Head Rx Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0189-2013·2012-11-14

    Clinical Diagnostic Solutions Recalls Boule Con-Diff Hematology Control Vials

    Clinical Diagnostic Solutions is recalling specific lots of Boule Con-Diff Hematology Control vials due to a received complaint.

    Product
    Boule Con-Diff Hematology Control For in vitro diagnostic use as a control to monitor the performance of multi-parameter hematology instruments.
    Category
    Medical Device
    Distribution
    31 states
  • LowFDA (Drugs)·D-048-2013·2012-11-14

    FDA Recalls Subpotent AcneFree Benzoyl Peroxide Cleanser

    Valeant Pharmaceuticals is recalling AcneFree Severe Maximum Strength Acne Pore Cleanser because the benzoyl peroxide ingredient is subpotent and the label contains errors.

    Product
    AcneFree Severe Maximum Strength Acne Pore Cleanser (benzoyl peroxide 5% w/v), 3 oz (85 g) canister, Dist. by: University Medical Pharmaceuticals Corp., Irvine, CA 92618, UPC 7 88521 13350 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0248-2013·2012-11-14

    Zimmer Kopf Adapter S Sterile Recalled for Label Discrepancies

    Zimmer Inc. is correcting patient labels for Kopf Adapter S Sterile products manufactured before March 2010 due to reference and lot number discrepancies.

    Product
    Kopf Adapter S Sterile, Rx
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0220-2013·2012-11-14

    Zimmer Fitmore Hip Stem Label Correction for Reference and Lot Discrepancies

    Zimmer Inc. is correcting patient labels for Fitmore Hip Stems manufactured before March 2010 due to discrepancies between product and patient labels regarding reference and lot numbers.

    Product
    Fitmore" Hip Stem
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0214-2013·2012-11-14

    Alloclassic SL-Offset Stem Patient Labels Corrected for Number Discrepancies

    Zimmer is correcting patient labels on 126 Alloclassic SL-Offset Stems made before March 2010 after four complaints that their reference and lot numbers differed from the correct product labels.

    Product
    Alloclassic¿ SL-Offset Stem sterile, Rx
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-042-2013·2012-11-14

    Valeant Recalls Subpotent AcneFree 24 Hour Clearing System

    Valeant Pharmaceuticals is recalling AcneFree 24 Hour Clearing System cartons because the benzoyl peroxide active ingredient is subpotent and the labels contain errors regarding inactive ingredients.

    Product
    AcneFree 24 Hour Clearing System containing 1-count 4 fl oz (118 mL) Oil-Free Purifying Cleanser (benzoyl peroxide 2.5% w/v) AFCS-0101-00, 1-count 4 fl oz (118 mL) Renewing Toner AFCS-0201-01, and 1-count 2 fl oz (59 mL) Repair Lotion (benzoyl peroxide 3.7% w/v) AFCS-0301-00 per
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·13034·2012-11-13

    Rec-Out Recalls Columbus Folding Camping Chairs Due to Mold Presence

    Rec-Out is recalling Columbus folding camping chairs sold at Big 5 Sporting Goods because they contain mold that could cause infections in vulnerable individuals.

    Product
    Folding Camping Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13036·2012-11-13

    Powermate Sx 5500 Portable Generators Recalled for Fire Hazard

    Pramac America is recalling Powermate Sx 5500 portable generators because a defective fuel filter allows gasoline to leak, posing a fire hazard.

    Product
    Powermate Sx 5500 portable generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V527000·2012-11-08

    Chrysler Recalls Jeep Liberty and Grand Cherokee for Airbag Defect

    Chrysler is recalling specific 2002-2004 Jeep Liberty and Grand Cherokee vehicles because a component failure may cause airbags to deploy unexpectedly.

    Product
    JEEP — JEEP LIBERTY, GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13033·2012-11-08

    Monessen Hearth Systems Recalls Gas Fireplaces Due to Fire Risk

    Monessen Hearth Systems is recalling about 15,000 gas fireplaces and inserts because a control component may prevent lighting while gas continues to flow, posing a fire hazard.

    Product
    Signature Command™ (electronically) Controlled Direct and B-Vent Gas Fireplaces and Inserts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13031·2012-11-08

    LG Electric Ranges Recalled Due to Burn and Fire Hazards

    LG Electronics is recalling about 161,000 electric ranges because burners may fail to turn off or heat unexpectedly, posing burn and fire risks.

    Product
    LG Electric Ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13705·2012-11-08

    2013 Diamondback Steilacoom RCX Bicycles Recalled for Crash Hazard

    CPSC recalls about 40 2013 Diamondback Steilacoom RCX bicycles because incorrect headset parts could cause the steerer tube to fail, leading to a crash.

    Product
    2013 Diamondback Steilacoom RCX bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13032·2012-11-08

    LaJobi Recalls Graco Glider Rockers Due to Base Breakage and Fall Hazard

    LaJobi is recalling Graco-branded Avalon and CNS Box 2 glider rockers because the base can crack or break, posing a fall hazard. Consumers should stop using the products and contact LaJobi for a free replacement base.

    Product
    Graco®-branded Avalon Glider Rockers with Ottoman and Complete Nursery Solution (CNS) Box 2 / Katelyn Nursery Solution Glider Rockers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0557-2013·2012-11-07

    Smith Dairy Peanut Butter Brownie Crunch Ice Cream Recalled for Sunland Peanut Butter

    Smith Dairy Products is recalling 3-gallon tubs of Peanut Butter Brownie Crunch ice cream because the peanut butter used was supplied by Sunland, Inc.

    Product
    SD Peanut Butter Brownie Crunch 3 Gallon MFD. BY SMITH DAIRY PRODUCTS COMPANY, ORRVILLE, OHIO 44667 1-800-778-7078.
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0544-2013·2012-11-07

    Sunland Peanut Products Recalled Due to Potential Salmonella Contamination

    Sunland, Inc. is voluntarily recalling specific peanut products, including shelled salted Valencia peanuts, because they may be contaminated with Salmonella.

    Product
    Sunland Shelled Salted Valencia Peanuts, 18 oz, UPC 0-48687-15909-3.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0542-2013·2012-11-07

    Sunland Peanut Products Recalled for Potential Salmonella Contamination

    Sunland, Inc. is voluntarily recalling peanut products, including shelled raw Valencia peanuts, due to potential Salmonella contamination.

    Product
    Sunland Shelled Raw Valencia Peanuts 3 lb UPC 0-48687-13212-6.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-038-2013·2012-11-07

    FDA Recalls Unapproved X-Rock 3 Day Pill For Men

    Coral Rock Man, Inc. is recalling X-Rock 3 Day Pill For Men because the product was marketed without an approved NDA/ANDA and tested positive for Sildenafil and analogs.

    Product
    X-ROCK 3 Day Pill For Men, supplied in 1 and 2 capsule blister packs and 6, 12 and 24 count bottles, UPC 0 00309 50792 7, Distributed by: MATE Enterprises, Miami, Florida 33139, Some labeled as: Manufactured by CRM Laboratories, Distributed by XRock Industries, Ft. Lauderdale, F
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-037-2013·2012-11-07

    X-ROCK For Men Recalled for Unapproved Prescription Drug Ingredients

    XRock Industries is recalling X-ROCK For Men dietary supplements because testing revealed the presence of unapproved prescription drug ingredients.

    Product
    X-ROCK For Men, Dietary Supplement, Manufactured by CRM Laboratories, Distributed by XRock Industries, PO Box 120863, Ft. Lauderdale, FL 33312, 0 00309 50792 7. UPC on labeling is: 0 00309 50792 7. UPC in Press Release is: 0030950792.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0572-2013·2012-11-07

    Xan Confections Recalls Peanut Butter Chocolate Confections Due to Salmonella Risk

    Xan Confections is voluntarily recalling 13 peanut butter chocolate products because the peanut butter supplier, Sunland, Inc., recalled its products due to potential Salmonella contamination.

    Product
    Chocolate, confections. Bulk Peanut Butter Crunch LadybuG, item number 090. 15 peices per case.
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-0524-2013·2012-11-07

    Sunland Peanut Products Recalled Due to Potential Salmonella Contamination

    Sunland, Inc. is voluntarily recalling specific peanut products, including Salted and Roasted Valencia Peanuts, because they may be contaminated with Salmonella.

    Product
    Sunland Salted and Roasted Valencia Peanuts, 1 lb, UPC 48687122066.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-039-2013·2012-11-07

    Z-ROCK Male Supplement Recalled for Unapproved Sildenafil Content

    Coral Rock Man, Inc. is recalling Z-ROCK All Natural Male Supplement because testing revealed the presence of Sildenafil and its analogs, which were not approved in the product.

    Product
    Z-ROCK All Natural Male Supplement. 1 capsule blister pack, UPC 0 00309 50792 7, Distributed by Zrock USA PO Box 668297, Pompano Beach, FL 33066
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0543-2013·2012-11-07

    Sunland Peanut Products Recalled Due to Potential Salmonella Contamination

    Sunland, Inc. is voluntarily recalling specific peanut products, including shelled roasted Valencia peanuts, because they may be contaminated with Salmonella.

    Product
    Sunland Shelled Roasted Valencia Peanuts, 18 oz, UPC 0-48687-14909-4.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0547-2013·2012-11-07

    Sunland Peanut Products Recalled Due to Potential Salmonella Contamination

    Sunland, Inc. is voluntarily recalling specific peanut products, including Valencia Roasted & Salted Peanuts, because they may be contaminated with Salmonella.

    Product
    Sunland Valencia Roasted & Salted Peanuts, 2lb UPC 0-48687-12105-2.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0562-2013·2012-11-07

    Harry & David Creamy Raspberry Peanut Spread Recalled for Salmonella Risk

    Harry & David is recalling Creamy Raspberry Peanut Spread jars and specific gift baskets due to potential Salmonella contamination.

    Product
    Harry & David Creamy Raspberry Peanut Spread, 12 oz. jars, labeled in part: "HARRY & DAVID CREAMY RASPBERRY PEANUT SPREAD***NET WT. 12 OZ. (340g)***INGREDIENTS: ROASTED PEANUTS, SUGAR, RASPBERRY COMPOUND***MADE FOR: HARRY AND DAVID MEDFORD, OR 97501***7 80994 73872 0***" The 1
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0533-2013·2012-11-07

    Sunland Peanuts Recalled for Potential Salmonella Contamination

    Sunland, Inc. is voluntarily recalling raw and roasted peanuts due to potential Salmonella contamination. The recall covers products distributed nationwide, in Canada, and in France.

    Product
    Sunland Raw Valencia Peanuts, 25 lb Item 104; 1 lb UPC 0-48687-10206-8; 2 lb UPC 0-48687-10215-0.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0540-2013·2012-11-07

    Sunland Salted Organic Peanuts Recalled Due to Salmonella Contamination Risk

    Sunland, Inc. is voluntarily recalling Salted Organic Peanuts because they may be contaminated with Salmonella. The products were distributed nationwide, in Canada, and in France.

    Product
    Sunland Salted Organic Peanuts, 1 lb UPC 0-48687-20206-5
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0571-2013·2012-11-07

    Xan Confections Recalls Peanut Butter Chocolate Due to Salmonella Risk

    Xan Confections is voluntarily recalling 13 peanut butter chocolate products because the supplier's peanut butter may be contaminated with Salmonella.

    Product
    Chocolate, confections. Bulk Peanut Butter LadybuG, item number 296.15pieces per case.
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-0548-2013·2012-11-07

    Sunland Peanut and Nut Butter Products Recalled for Salmonella Risk

    Sunland, Inc. is voluntarily recalling specific peanut and nut butter products because they may be contaminated with Salmonella.

    Product
    The Nut Shop Roasted Valencia Peanuts, 7 oz, Item 22601.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0564-2013·2012-11-07

    Dean Foods Recalls Albertsons Peanut Butter Cup Ice Cream Due to Salmonella Risk

    Dean Foods is recalling Albertsons Brand Peanut Butter Cup Ice Cream because it contains a peanut butter ingredient that may be contaminated with Salmonella.

    Product
    Albertsons Brand Peanut Butter Cup Ice Cream, 1.5 Quarts (1.42L), commonly called a 48 fl oz container. Peanut Butter Cup Ice Cream, (Vanilla ice cream with peanut butter cup pieces, fudge and peanut butter swirls); 1.5 QTS (1.42L), (UPC Code 0 41163 45891 8 for Albertsons
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-0546-2013·2012-11-07

    Sunland Raw Peanuts Recalled for Potential Salmonella Contamination

    Sunland, Inc. is recalling raw peanuts and other nut products due to potential Salmonella contamination. The recall covers products distributed nationwide, in Canada, and France.

    Product
    Sunland Valencia Raw Peanuts, 25 lb UPC 0-48687-10102-3; 10 lb UPC 10103; 2 lb UPC 0-48687-10105-4; 5 lb UPC 0-48687-10104-7.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0559-2013·2012-11-07

    Harry & David Crunchy Almond and Peanut Butter Recalled for Salmonella Risk

    Harry & David is recalling 15,264 jars of Crunchy Almond and Peanut Butter and associated gift baskets due to potential Salmonella contamination.

    Product
    Harry & David Crunchy Almond and Peanut Butter, 12 oz. jar., labeled in part: "HARRY & DAVID CRUNCHY ALMOND AND PEANUT BUTTER***NET WT. 12 OZ. (340g)***INGREDIENTS: ROASTED ALMONDS, ROASTED PEANUTS, SEA SALT.***MADE FOR HARRY AND DAVID MEDFORD, OR 97501***7 80994 73873 7***" T
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0523-2013·2012-11-07

    Sunland Peanut Products Recalled Due to Potential Salmonella Contamination

    Sunland, Inc. is voluntarily recalling specific peanut products, including Roasted Valencia Peanuts, because they may be contaminated with Salmonella.

    Product
    Sunland Roasted Valencia Peanuts, 2 oz, UPC 48687112166.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0541-2013·2012-11-07

    Sunland Salted Valencia Peanuts Recalled for Salmonella Contamination Risk

    Sunland, Inc. is voluntarily recalling Salted Valencia Peanuts because they may be contaminated with Salmonella. The recall covers products distributed nationwide, in Canada, and France.

    Product
    Sunland Salted Valencia Peanuts, 50 lb UPC 0-48687-12101-4; 25 lb UPC 0-48687-12102-1; 10 lb UPC 0-48687-12103-8; 5 lb UPC 0-48687-12104-5; 12 oz UPC 0-48687-12210-3; 2 lb UPC 0-48687-12215-8; 2 oz UPC 0-48687-12216-5; 4 oz UPC 0-48687-12217-2.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0528-2013·2012-11-07

    Sunland Peanut and Nut Butter Products Recalled for Salmonella Risk

    Sunland, Inc. is voluntarily recalling peanut and nut butter products, as well as raw and roasted peanuts, due to potential Salmonella contamination.

    Product
    Sunland Raw Organic Valencia Peanuts, 50 lb UPC 4868700103
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0549-2013·2012-11-07

    Sunland Recalls Peanuts and Nut Butters Due to Salmonella Risk

    Sunland, Inc. is voluntarily recalling specific peanut and nut butter products because they may be contaminated with Salmonella.

    Product
    The Nut Shop Salted and Roasted Valencia Peanuts, 7 oz, Item 22602.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0534-2013·2012-11-07

    Sunland Raw Valencia Peanuts Recalled for Potential Salmonella Contamination

    Sunland, Inc. is recalling Raw Valencia Peanuts due to potential Salmonella contamination. The recall covers products distributed nationwide, in Canada, and France.

    Product
    Sunland Raw Valencia Peanuts - Export, 50 lbs UPC 4868700101.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0526-2013·2012-11-07

    Sunland recalls almond, peanut, and cashew butter products due to Salmonella risk

    Sunland, Inc. is voluntarily recalling almond, peanut, and cashew butter products, tahini, and roasted blanched peanut products manufactured between May 2010 and September 2012 because they may be contaminated with Salmonella.

    Product
    Sunland Organic Raw Inshell, 25 lb, UPC 10107.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0536-2013·2012-11-07

    Sunland Peanut Products Recalled Due to Potential Salmonella Contamination

    Sunland, Inc. is voluntarily recalling specific peanut products, including Roasted In Shell Peanuts, because they may be contaminated with Salmonella.

    Product
    Sunland Roasted In Shell Peanuts, 25 lb, UPC 0-48687-11102-2
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0560-2013·2012-11-07

    Harry & David Creamy Banana Peanut Spread Recalled for Salmonella Risk

    Harry & David is recalling 36,060 jars of Creamy Banana Peanut Spread due to potential Salmonella contamination. The product was sold nationwide and in Canada.

    Product
    Harry & David Creamy Banana Peanut Spread, 12 oz. jars labeled in part: "HARRY & DAVID CREAMY BANANA PEANUT SPREAD***NET WT. 12 OZ. (340g)***INGREDIENTS: ROASTED PEANUTS, SUGAR, BANANA COMPOUND***MADE FOR: HARRY AND DAVID MEDFORD, OR 97501***7 80994 73871 3***" The 12 oz. jars
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0531-2013·2012-11-07

    Sunland Peanut Products Recalled Due to Salmonella Contamination Risk

    Sunland, Inc. is voluntarily recalling peanut products, including raw shelled organic peanuts, due to potential Salmonella contamination.

    Product
    Sunland Raw Shelled Organic Peanuts, 30 lb Item 403.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0574-2013·2012-11-07

    Xan Confections Recalls Peanut Butter Chocolate Due to Salmonella Risk

    Xan Confections is voluntarily recalling 13 peanut butter chocolate products because the supplier's peanut butter may be contaminated with Salmonella.

    Product
    Chocolate, confections. Bulk Peanut Butter Jewel, item number 096. 24 pieces per case.
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-0569-2013·2012-11-07

    Xan Confections Recalls Mini BigMouth Chocolate Confections Due to Salmonella Risk

    Xan Confections is voluntarily recalling Mini BigMouth chocolate confections because they may be contaminated with Salmonella from a peanut butter supplier.

    Product
    Mini BigMouth: Chocolate, confections. 1) Bulk Milk Mini BigMouth, item number 093. 15 pieces per case; 2) 4-Piece Mini BigMouth, item number 284, 48 pieces per case: 3) 6-Piece Mini BigMouth, item number 002, 72 pieces per case
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-0556-2013·2012-11-07

    Smith Dairy Peanut Butter Ice Cream Recalled for Peanut Butter Source

    Smith Dairy Products is recalling peanut butter ice cream because the peanut butter crunch candies used in the product were made with peanut butter from Sunland, Inc.

    Product
    Peanut Butter Ice Cream (1.75 Qt & Half Gallon) Peanut butter ice cream with a peanut butter ribbon and a delightful crunch candy Artificial flavor added MFD. BY SMITH DAIRY PRODUCTS COMPANY, ORRVILLE, OHIO 44667 1-800-778-7078. Sold under the following names: SMITH'S Peanut But
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0520-2013·2012-11-07

    Sunland Peanuts and Nuts Recalled for Potential Salmonella Contamination

    Sunland, Inc. is voluntarily recalling specific peanut and nut products due to potential Salmonella contamination. The recall covers products distributed nationwide and in Canada and France.

    Product
    Mega Raw Oriental Produce Wholesaler- Valencia Peanuts, No UPC, Item numbers M10101.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0522-2013·2012-11-07

    Sunland Recalls Raw Peanuts Due to Potential Salmonella Contamination

    Sunland, Inc. is recalling Natural Value Raw Peanuts because they may be contaminated with Salmonella. The products were distributed nationwide, in Canada, and in France.

    Product
    Natural Value Raw Peanuts, 30 lb Item number 910169.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0538-2013·2012-11-07

    Sunland Salted In-Shell Peanuts Recalled for Salmonella Contamination Risk

    Sunland, Inc. is recalling Salted In-Shell Peanuts because they may be contaminated with Salmonella. The recall covers products with Best By Dates from October 12, 2012, through April 12, 2013.

    Product
    Sunland Salted In-Shell Bulk in Box, 25 lb UPC 0-48687-12108-3.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0535-2013·2012-11-07

    Sunland Recalls Peanuts and Nuts Due to Salmonella Contamination Risk

    Sunland, Inc. is voluntarily recalling specific peanut and nut products because they may be contaminated with Salmonella.

    Product
    Sunland Raw Virginia Reg Jumbo InShell, 50 lb UPC 0-48687-76101-2
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0527-2013·2012-11-07

    Sunland Organic Roasted In-Shell Peanuts Recalled for Salmonella Risk

    Sunland, Inc. is recalling Organic Roasted In-Shell Peanuts because they may be contaminated with Salmonella. The recall covers products distributed nationwide, in Canada, and France.

    Product
    Sunland Organic Roasted In Shell Peanuts, 25 lb UPC 11109, 2 lb UPC 48687791057.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0530-2013·2012-11-07

    Sunland Peanuts Recalled Due to Potential Salmonella Contamination

    Sunland, Inc. is recalling raw and roasted peanuts and other nut products due to potential Salmonella contamination.

    Product
    Sunland Raw In-Shell peanuts, 50 lb UPC 0-48687-10101-6 .
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0521-2013·2012-11-07

    Sunland Peanut and Nut Butter Products Recalled for Salmonella Risk

    Sunland, Inc. is voluntarily recalling peanut, almond, and cashew butter products, as well as tahini and roasted peanuts, due to potential Salmonella contamination.

    Product
    Mega Raw Oriental Produce Wholesaler- Virginia Peanuts, No UPC, Item numbers M76101.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0532-2013·2012-11-07

    Sunland Peanut and Nut Butter Products Recalled for Salmonella Risk

    Sunland, Inc. is voluntarily recalling peanut, almond, and cashew butter products, tahini, and peanuts due to potential Salmonella contamination.

    Product
    Sunland Raw Shelled Peanuts, 50 lbs, Item 400.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0570-2013·2012-11-07

    Xan Confections Recalls Peanut Butter Chocolate Due to Salmonella Risk

    Xan Confections is voluntarily recalling 13 peanut butter chocolate products due to potential Salmonella contamination from a supplier recall.

    Product
    Chocolate, confections. Bulk Dark Mini BigMouth, item number 094. Each case contains 15 pieces.
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-0563-2013·2012-11-07

    Dean Foods Recalls Albertsons Peanut Butter Chocolate Ice Cream Due to Salmonella Risk

    Dean Foods is recalling Albertsons Peanut Butter Chocolate Ice Cream because the peanut butter ingredient may be contaminated with Salmonella.

    Product
    Albertsons Brand Peanut Butter Chocolate Ice Cream, 1.5 Quarts (1.42L), commonly called a 48 fl oz container. Peanut Butter Chocolate Ice Cream (Chocolate ice cream with a peanut butter swirl); 1.5 QTS (1.42L), (UPC Code: 0 41163 45903 8 for Albertsons Peanut Butter Chocola
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-0537-2013·2012-11-07

    Sunland Peanut Products Recalled for Potential Salmonella Contamination

    Sunland, Inc. is voluntarily recalling specific peanut products, including Roasted Valencia Peanuts, due to potential Salmonella contamination.

    Product
    Sunland Roasted Valencia Peanuts, 50 lb UPC 0-48687-11101-5; 10 lb UPC 0-48687-11103-9; 5 lb UPC 0-48687-11104-4; 2 lb UPC 0-48687-11105-3; 1 lb UPC 0-48687-11206-7; 12 oz UPC 0-48687-11210-4; 2 lb UPC 0-48687-11215-9; 4 oz UPC 0-48687-11217-3.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0573-2013·2012-11-07

    Xan Confections Recalls Peanut Butter Chocolate Due to Salmonella Risk

    Xan Confections is voluntarily recalling 13 peanut butter chocolate products because the peanut butter supplier, Sunland, Inc., recalled its products due to potential Salmonella contamination.

    Product
    Chocolate, confections. Bulk Mini Peanut Butter Crunch LadybuG, item number 115. 24 pieces per case.
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0124-2013·2012-11-07

    HeartSine Samaritan 300/300P PAD Devices Recalled for Malfunction

    Heartsine is recalling 81,982 Samaritan 300/300P PAD devices because they may turn on or off unexpectedly, potentially preventing therapy delivery during cardiac arrest.

    Product
    HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501 to 0700032917; 08A00035000 to 10A0070753; 10C00200000 to 10C00210106 Product Usage: Samaritan 300/300P PAD is indicated for use on victims of sudden cardiac arrest who are exhibiting the following sign
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0175-2013·2012-11-07

    Ventlab AirFlow Resuscitator Recalled for Inlet Valve Leakage

    Ventlab Corporation is recalling 14,602 AirFlow Resuscitators due to possible volume leakage through the inlet valve during bag compressions.

    Product
    AirFlow Resuscitator, Adult Resuscitator, AF1000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028 The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of re
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0576-2013·2012-11-07

    Xan Confections Recalls Peanut Butter Chocolate Due to Salmonella Risk

    Xan Confections is voluntarily recalling 13 peanut butter chocolate products due to potential Salmonella contamination from a supplier recall.

    Product
    Chocolate, confections. Bulk Dark BigMouth, item number 232. 8 peices per cases.
    Category
    Food
    Distribution
    8 states

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