The Recall Desk

Archive

April 2015 recalls

1,319 recalls were announced in April 2015.

What the numbers show

Critical
109
Severe
527
High
388
Moderate
278
Low
17

Of the 1,319 recalls this month scored against our rubric, 8% are Critical, 40% are Severe.

Which agencies issued them

501–600 of 1319

  • HighFDA (Drugs)·D-724-2015·2015-04-29

    Attix Pharmaceuticals Recalls Hydroxyzine HCl Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling Hydroxyzine HCl active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.

    Product
    Hydroxyzine HCl active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-528-2015·2015-04-29

    Atovaquone API Recalled for Potential Penicillin Cross-Contamination

    Attix Pharmaceuticals is recalling Atovaquone active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.

    Product
    Atovaquone active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-644-2015·2015-04-29

    Attix Pharmaceuticals Recalls D-Penicillamine Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling D-Penicillamine active pharmaceutical ingredient due to potential penicillin cross-contamination from inadequate facility separation.

    Product
    D-Penicillamine active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-502-2015·2015-04-29

    Adapalene API Recalled for Potential Penicillin Cross Contamination

    Attix Pharmaceuticals is recalling all lots of Adapalene active pharmaceutical ingredient distributed between January 2012 and February 2015 due to potential penicillin cross-contamination.

    Product
    Adapalene active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1482-2015·2015-04-29

    Wright Medical Recalls Crosscheck Plating System Due to Spec Failures

    Wright Medical Technology is recalling 51 units of the Crosscheck Plating System because dimensional specifications are out of range, posing a risk of intraoperative malfunction.

    Product
    CROSSCHECK(R) Plating system, HOCKEY STICK CX Plate, Left, REF CCP-HSX1L. Orthopedic use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1518-2015·2015-04-29

    Hospira LifeCare PCA Infusion System Recalled for Door Design Flaw

    Hospira is recalling 38,882 LifeCare PCA infusion systems because the clear plastic door design allows excessive flexing, permitting unauthorized access to medication vials.

    Product
    The LifeCare PCA infusion system with Hospira MedNet software allows clinicians, or patients, to (self) Administer analgesia within clinician programmed and/or hospital defined medication limits.
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Food)·F-2022-2015·2015-04-29

    Giant Eagle Recalls Japanese Breaded Cod Fillet for Undeclared Soy

    Giant Eagle is recalling Japanese Breaded Cod Fillet because it contains undeclared soy, a major food allergen.

    Product
    Giant Eagle Japanese Breaded Cod Fillet various weights Contains: Fish, Wheat, Milk, Egg Dist. By: Giant Eagle Mkts. Co., Pittsburgh, PA 15238 Sell by: (up to and including) 3/26/2015 Sold on foam trays with flexible plastic overwrap.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1488-2015·2015-04-29

    Wright Medical Recalls Crosscheck Plating System Due to Dimensional Defects

    Wright Medical Technology is recalling 148 units of the Crosscheck Plating system because specific dimensions are out of specification, posing a risk of intraoperative malfunction.

    Product
    CROSSCHECK(R) Plating system, LAPIDUS CX Plate, 2mm Step, Left, REF CCP-LPX2L. Orthopedic use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-782-2015·2015-04-29

    Attix Pharmaceuticals Recalls Methimazole Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling methimazole active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging. The product was distributed nationwide to compounding pharmacies and research organizations.

    Product
    Methimazole active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-538-2015·2015-04-29

    Attix Pharmaceuticals Recalls Benoxinate HCl Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling Benoxinate HCl active pharmaceutical ingredient due to potential penicillin cross-contamination from inadequate facility separation.

    Product
    Benoxinate HCl active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-871-2015·2015-04-29

    Attix Pharmaceuticals Recalls Pyrazinamide Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling Pyrazinamide active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.

    Product
    Pyrazinamide active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2014-2015·2015-04-29

    Ricos Tostaditos Chiviricos Recalled for Undeclared Wheat and Soy Oil

    Ricos Tostaditos, Inc. is recalling 4,000 bags of Chiviricos Fried Dough due to undeclared wheat and soy oil allergens.

    Product
    RICOS Tostaditos Chiviricos Fried Dough Crispy and Delicious Net Wt. 2-1/4 oz. (64g)
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2013-2015·2015-04-29

    Ateeco Recalls Mrs. T's Pierogies Due to Plastic Contamination

    Ateeco, Inc. is voluntarily recalling specific lots of Mrs. T's Mozzarella, Tomato & Basil Pierogies due to plastic contamination that may pose a choking hazard.

    Product
    Mrs. Ts Pierogies, Net Wt 16 oz (1 lb) 456 g,12 Pieces/ Carton 12 Cartons/ Case, frozen, Best By: 05/20/16, 07/15/16, 08/27/16 UPC: 4116400042
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1464-2015·2015-04-29

    DiaSorin Recalls PRO-Trac II Tacrolimus ELISA Kits Due to Instability

    DiaSorin is recalling 451 PRO-Trac II Tacrolimus ELISA kits because instability may cause falsely elevated patient results.

    Product
    DiaSorin, PRO-Trac II Tacrolimus ELISA kit, REF 32400 and 32400-CN. Product Usage: The PRO-Trac II Tacrolimus ELISA kit is an in vitro reagent system intended for the quantitative determination of tacrolimus (Prografl, FK506) and some metabolites in human EDT A or heparinized w
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Drugs)·D-769-2015·2015-04-29

    Attix Pharmaceuticals Recalls Loratadine API Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling Loratadine active pharmaceutical ingredient due to potential penicillin cross-contamination from inadequate facility separation.

    Product
    Loratadine active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-869-2015·2015-04-29

    Progesterone API Recalled for Potential Penicillin Cross-Contamination

    Attix Pharmaceuticals is recalling progesterone active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.

    Product
    Progesterone Ultra-Micronized active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1483-2015·2015-04-29

    Wright Medical Recalls Crosscheck Plating System Due to Dimensional Defects

    Wright Medical Technology is recalling 52 units of the Crosscheck Plating System because dimensional specifications are out of range, posing a risk of intraoperative malfunction.

    Product
    CROSSCHECK(R) Plating system, HOCKEY STICK CX Plate, Right, REF CCP-HSX1R. Orthopedic use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2029-2015·2015-04-29

    Dairy Farmers of America Recalls Borden Good 2 Gether Snack Trays

    Dairy Farmers of America is recalling Borden Good 2 Gether snack trays due to a potential hard plastic fragment hazard.

    Product
    Borden Good 2 Gether, Colby Jack Cheese & Pretzels, UPC: 5300001113, Net Wt 2 0z (57 g), Dist. By DFA Dairy Farmers of America, PO Box 909700, Kansas City, MO 64190.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Drugs)·D-939-2015·2015-04-29

    Tranilast API Recalled for Potential Penicillin Cross-Contamination

    Attix Pharmaceuticals is recalling Tranilast active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.

    Product
    Tranilast active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-786-2015·2015-04-29

    Attix Pharmaceuticals Recalls Methotrexate Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling Methotrexate USP active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.

    Product
    Methotrexate USP active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2019-2015·2015-04-29

    Rising Moon Organics Spinach and Cheese Ravioli Recalled for Listeria

    Carmel Food Group is recalling Rising Moon Organics Spinach & Cheese Ravioli because the spinach used contained Listeria monocytogenes.

    Product
    Rising Moon Organics Spinach & Cheese Ravioli; Net Wt 8 oz. (227g) UPC 7 85030 55561 3 Distributed by Rising Moon Organics 313 Iron Horse Way Providence, RI 02908
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-884-2015·2015-04-29

    Attix Pharmaceuticals Recalls Roflumilast API Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling Roflumilast active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.

    Product
    Roflumilast active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2031-2015·2015-04-29

    Silver Lake Easter Egg Cookies Recalled for Undeclared Egg Allergen

    Silver Lake Cookie Co. is recalling Easter Egg Cookies because they contain undeclared egg, a major food allergen.

    Product
    Silver Lake Easter Egg Cookies, NET WT. 8 OZ (226g), UPC 0 37695 49817 1. Silver Lake Cookie Company, Inc. 141 Freeman Ave., Islip, NY 11751. MADE IN THE USA.
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-2024-2015·2015-04-29

    Giant Eagle Recalls Italian Subs for Undeclared Egg Allergen

    Giant Eagle is recalling 4,671 units of GetGo 7-inch Italian subs sold in Maryland, Ohio, Pennsylvania, and West Virginia due to an undeclared egg allergen.

    Product
    GetGo GNG 7 Inch Italian Sub Sell By: (up to and including) 04/02/15 Net Wt: 6.0 Oz. Contains: Soy, Milk, Wheat UPC: 25567 20399 GetGo from Giant Eagle Distributed by Giant Eagle, Inc., Pittsburgh, PA 15238 Sandwich is wrapped in plastic.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1486-2015·2015-04-29

    Wright Medical Recalls Crosscheck Plating System Due to Dimensional Defects

    Wright Medical Technology is recalling 102 units of the Crosscheck Plating System because dimensional specifications are out of tolerance, posing a risk of intraoperative malfunction.

    Product
    CROSSCHECK(R) Plating system, LAPIDUS CX Plate, 1mm Step, Left, REF CCP-LPX1L. Orthopedic use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-863-2015·2015-04-29

    Attix Pharmaceuticals Recalls Procainamide HCl Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling Procainamide HCl active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.

    Product
    Procainamide HCl active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-809-2015·2015-04-29

    Attix Pharmaceuticals Recalls Mupirocin API Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling Mupirocin active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.

    Product
    Mupirocin active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-780-2015·2015-04-29

    Attix Pharmaceuticals Recalls Metaxalone API Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling Metaxalone active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.

    Product
    Metaxalone active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-608-2015·2015-04-29

    D-Cycloserine API Recalled for Potential Penicillin Cross-Contamination

    Attix Pharmaceuticals is recalling D-Cycloserine active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.

    Product
    D-Cycloserine active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-613-2015·2015-04-29

    Attix Pharmaceuticals Recalls Dapiprazole HCl Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling Dapiprazole HCl active pharmaceutical ingredient due to potential penicillin cross-contamination from repackaging in a shared facility.

    Product
    Dapiprazole HCl active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1487-2015·2015-04-29

    Wright Medical Recalls Crosscheck Plating System Due to Specification Defects

    Wright Medical Technology is recalling 142 units of the Crosscheck Plating system because dimensional specifications are out of tolerance, posing a risk of intraoperative malfunction.

    Product
    CROSSCHECK(R) Plating system, LAPIDUS CX Plate, 1mm Step, Right, REF CCP-LPX1R. Orthopedic use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-847-2015·2015-04-29

    Attix Pharmaceuticals Recalls Polidocanol Due to Penicillin Cross Contamination Risk

    Attix Pharmaceuticals is recalling Polidocanol active pharmaceutical ingredient due to potential penicillin cross-contamination from inadequate facility separation.

    Product
    Polidocanol active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-492-2015·2015-04-29

    Attix Pharmaceuticals Recalls 4-Aminopyridine Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling 4-Aminopyridine active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.

    Product
    4-Aminopyridine active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-833-2015·2015-04-29

    Attix Pharmaceuticals Recalls Paroxetine Active Ingredient Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling paroxetine active pharmaceutical ingredient repackaged between January 2012 and February 2015 due to potential penicillin cross-contamination.

    Product
    Paroxetine active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-550-2015·2015-04-29

    Attix Pharmaceuticals Recalls Budesonide API Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling budesonide active pharmaceutical ingredient due to potential penicillin cross-contamination from inadequate facility separation.

    Product
    Budesonide active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1475-2015·2015-04-29

    Churchill Medical Systems Recalls 7-inch High Pressure Extension Sets

    Churchill Medical Systems is recalling 6,850 units of 7-inch Standard Bore High Pressure Extension Sets due to a potential leak caused by insufficient bonding.

    Product
    7" Standard Bore High Pressure Ext Set, Product Code: CMS-809 Accessory device used to administer medical fluids
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-935-2015·2015-04-29

    Tolvaptan API Recalled for Potential Penicillin Cross Contamination

    Attix Pharmaceuticals is recalling Tolvaptan active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.

    Product
    Tolvaptan active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1490-2015·2015-04-29

    Wright Medical Recalls Crosscheck Plating System Due to Specification Defects

    Wright Medical Technology is recalling 167 units of the Crosscheck Plating System because dimensional specifications are out of tolerance, posing a risk of intraoperative malfunction.

    Product
    CROSSCHECK(R) Plating system, MTP NX Plate, Left, Recon, REF CCP-MPN2L. Orthopedic use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1468-2015·2015-04-29

    Churchill Medical Systems Recalls Bifurcated Extension Sets Due to Leaking Risk

    Churchill Medical Systems is recalling 100 Bifurcated Extension Sets because a defect may cause leaking. The sets are used to administer medical fluids.

    Product
    Bifircated Extension Set, Product Code: BN-828 Accessory device used to administer medical fluids
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1512-2015·2015-04-29

    Xpress System Pedicle Screw Assembly Recalled for Incorrect Laser Marking

    X Spine Systems Inc is recalling 14 units of Xpress System Pedicle Screw Assemblies because the laser marking on the yoke incorrectly states 7.5 x 55mm instead of 5.5 x 55mm.

    Product
    Xpress System Pedicle Screw Assembly, 5.5 x 55mm. An internal fixation device for spinal surgery consisting of rods, pedicle screw assemblies (screw, cap, yoke) and cross bar connector assemblies.
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1466-2015·2015-04-29

    Biomet Recalls Torque Limiting Handles for Spinal Fixation Devices

    Biomet Spine is recalling 874 Torque Limiting Handles used in spinal fixation due to supplier component updates.

    Product
    Torque Limiting Handle (Aspen/ Alpine) Model Number 6200-1109 Product Usage: Provides posterior fixation in the non-cervical spine with an interspinous fixation device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-967-2015·2015-04-29

    Tarmac Recalls Well at Walgreens Comfort Gel for Antimicrobial Failure

    Tarmac Products, Inc. is recalling Well at Walgreens Regular Strength Comfort Gel Cherry Flavor because the product failed the Antimicrobial Effectiveness Test.

    Product
    Well at Walgreens Regular Strength Comfort Gel Cherry Flavor, 12 fl oz (355 mL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1481-2015·2015-04-29

    Catheter Research Recalls Mislabeled HSG Trays and Catheters

    Catheter Research, Inc. is recalling 880 HSG trays and catheters because the flexible and shapeable catheters were mislabeled on the packaging.

    Product
    HSG Trays/HS 5F Catheter Combo; HSG Procedure Tray+ Shapeable 5F HSG catheter. For hysterosonography and hysterosalpingography, gynecological use.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1510-2015·2015-04-29

    Specialty Appliance Works Recalls Universal Nuts for Incorrect Stainless Steel Material

    Specialty Appliance Works is recalling Universal Nuts used in Herbst Appliances because they were made with 416 SS instead of the specified 303 SS.

    Product
    Upper Right Telescope Unibodies (5/pk) and Upper Left Telescope Unibodies (54/pk) A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1455-2015·2015-04-29

    DBX Mix Bone Void Filler Recalled for Potential Packaging Seal Defect

    Musculoskeletal Transplant Foundation is recalling 25 units of DBX Mix bone void filler because the outer packaging seal may not be fully intact.

    Product
    DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void filler.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1511-2015·2015-04-29

    Specialty Appliance Works Recalls Orthodontic Universal Nut Components

    Specialty Appliance Works is recalling TS ROC Crown Components because the Universal Nut was made with 416 SS instead of the specified 303 SS.

    Product
    TS ROC Crown Component 4UR (5/pk), TS ROC Crown Component 5UR (5/pk), TS ROC Crown Component 6UR (5/pk), TS ROC Crown Component 7UR (5/pk), TS ROC Crown Component 8UR (5/pk), TS ROC Crown Component 4LR (5/pk), TS ROC Crown Component 5LR (5/pk), TS ROC Crown Component 6LR (5/pk),
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1505-2015·2015-04-29

    Specialty Appliance Works Recalls MiniScope Mechanical Set Universal Nuts

    Specialty Appliance Works is recalling Universal Nuts for MiniScope Mechanical Sets because they were made with 416 stainless steel instead of the specified 303 stainless steel.

    Product
    Specialty MiniScope Mech. Set Size 18, Specialty MiniScope Mech. Set Size 21, and Specialty MiniScope Mech. Set Size 24 A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-929-2015·2015-04-29

    Attix Pharmaceuticals Recalls Ticarcillin Sodium/Potassium Clavulanate API Due to Stability Data Issues

    Attix Pharmaceuticals is recalling Ticarcillin Sodium/Potassium Clavulanate API because stability data does not support the printed expiry dates for lots distributed between 2012 and 2015.

    Product
    Ticarcillin Sodium/Potassium Clavulanate (30:1) active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1509-2015·2015-04-29

    Specialty Appliance Works Recalls Orthodontic Universal Nut Components

    Specialty Appliance Works is recalling Universal Nut components for Herbst Appliances because they were made with 416 SS instead of the specified 303 SS.

    Product
    TS Crown Component 4UR (5/pk), TS Crown Component 5UR (5/pk), TS Crown Component 6UR (5/pk), TS Crown Component 4LR (5/pk), TS Crown Component 5LR (5/pk), TS Crown Component 6LR (5/pk), TS Crown Component 4UL (5/pk), TS Crown Component 5UL (5/pk), TS Crown Component 4LL (5/pk), T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1504-2015·2015-04-29

    Specialty Appliance Works Recalls Orthodontic Herbst Appliance Nuts

    Specialty Appliance Works is recalling TS Herbst Nuts because they were manufactured with 416 stainless steel instead of the specified 303 stainless steel.

    Product
    TS Herbst Nuts with Backing (10/pk) and TS Herbst Nuts Universal (10/pk) A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1516-2015·2015-04-29

    PhotoMedex Recalls Iamin Medical Devices Due to Inconsistent Labeling

    PhotoMedex, Inc. is recalling Iamin Moist Dressings and Hydrating Gel because their labeling does not match the intended uses approved by the FDA.

    Product
    Iamin Moist Dressing and the Iamin Hydrating Gel: intended to cover a wound or burn on the skin, provide a moist wound environment and protect against abrasion, friction, desiccation and contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1479-2015·2015-04-29

    SpineFrontier Recalls MISquito Pedicle Screw System Surgical Technique Document

    SpineFrontier is recalling the MISquito Pedicle Screw System Surgical Technique document because it does not adequately convey the intended use of the Rod Caliper.

    Product
    SpineFrontier MISquito Percutaneous Pedicle Screw System Surgical Technique; Part Number: DOC80023. The Rod Caliper is a manual surgical instrument that may be used as part of the PedFuse Pedicle Screw System and its MISquito components during percutaneous, minimally invasive
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1503-2015·2015-04-29

    Specialty Appliance Works Recalls Orthodontic Universal Nuts Due to Material Error

    Specialty Appliance Works is recalling 14,428 Universal Nuts used in orthodontic Herbst Appliances because they were manufactured with 416 SS instead of the specified 303 SS.

    Product
    MiniScope Hst ROC Crown 15 Patient Kit, and MiniScope Herbst Crown 15 Patient Kit A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-966-2015·2015-04-29

    Tarmac Recalls Well at Walgreens Comfort Gel for Antimicrobial Failure

    Tarmac Products, Inc. is recalling 41,743 bottles of Well at Walgreens Maximum Strength Comfort Gel because the product failed the Antimicrobial Effectiveness Test.

    Product
    Well at Walgreens Maximum Strength Comfort Gel 12 FL OZ (355 mL) bottle,
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1454-2015·2015-04-29

    Focus Diagnostics Recalls Stratify JCV DxSelect Assay Due to False Positive Risk

    Focus Diagnostics is recalling 300 units of the Stratify JCV DxSelect assay (Lot 27333) because a non-conforming batch may cause false positive results.

    Product
    STRATIFY JCV DxSelect, Model No. EL1950. Assay for detection of antibodies to JC Virus in human serum or plasma. In Vitro diagnostic.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-2021-2015·2015-04-29

    Summit Import Recalls Preserved Duck Eggs for pH and Salt Standard Failures

    Summit Import Corporation is recalling Yang Sheng Preserved Duck Eggs because the product failed to meet required pH and salt standards.

    Product
    Yang Sheng Preserved Egg (Long-Lansing Duck Egg), each box contains 6 preserved eggs, each box weighs about 12 ounce (340g), Manufacturer: Ya Nong Co., Ltd, No. 181-1, Singdong Rd., Jhongli City, Taoyuan County, 320, Taiwan R.O.C., Product of Taiwan
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-1506-2015·2015-04-29

    Specialty Appliance Works Recalls Universal Nuts for Incorrect Material Composition

    Specialty Appliance Works is recalling Universal Nuts used in orthodontic Herbst Appliances because they were manufactured with 416 stainless steel instead of the specified 303 stainless steel.

    Product
    M-4 Mechanism Set 16 mm and M-4 Mechanism Set 19 mm A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1459-2015·2015-04-29

    Exactech Recalls Equinoxe 44mm Short Humeral Head Shoulder Implants

    Exactech, Inc. is recalling 112 Equinoxe 44mm Short Humeral Head shoulder implant components because incorrect outer and inner labeling may misidentify the device size.

    Product
    Equinoxe 44mm Short Humeral Head Catalog Number 310-01-44. Orthopedic shoulder implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1507-2015·2015-04-29

    Specialty Appliance Works Recalls Universal Nuts for Orthodontic Appliances

    Specialty Appliance Works is recalling Universal Nuts for orthodontic Herbst Appliances because they were made with 416 stainless steel instead of the specified 303 stainless steel.

    Product
    HTM Mechanism Set Set 16, HTH Mechanism Set Size 18, HTH Mechanism Set Size 21 and HTH Mechanism Set Size 24 A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-520-2015·2015-04-29

    Attix Pharmaceuticals Recalls Amoxicillin Trihydrate Due to Missing Stability Data

    Attix Pharmaceuticals is recalling Amoxicillin Trihydrate active pharmaceutical ingredient because stability data does not support the printed expiry dates.

    Product
    Amoxicillin Trihydrate active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1465-2015·2015-04-29

    Biomet Recalls Lineum HF Torque Handle Limit Due to Component Updates

    Biomet Spine is recalling 148 Lineum HF Torque Handle Limit units because the supplier withdrew the product for component updates or reconfiguration.

    Product
    Lineum HF Torque Handle Limit (Lineum) Model Number 14-525035 P_roduct Usage: Designed to facilitate reconstruction of the cervical and upper thoracic spine using bones screws, locking plugs, and various types of rods, hooks, and lateral connectors.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-968-2015·2015-04-29

    Tarmac Recalls Well at Walgreens Antacid Liquid for Failed Antimicrobial Test

    Tarmac Products, Inc. is recalling Well at Walgreens Regular Strength Antacid Liquid because the product failed the Antimicrobial Effectiveness Test.

    Product
    Well at Walgreens Regular Strength Antacid Liquid, Mint Flavor 12 FL OZ (355 mL) bottle
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-707-2015·2015-04-29

    Attix Pharmaceuticals Recalls Homatropine Methylbromide Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling Homatropine Methylbromide active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.

    Product
    Homatropine Methylbromide active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1502-2015·2015-04-29

    Herbst Universal Nut Recalled for Incorrect Stainless Steel Material

    Specialty Appliance Works is recalling Herbst Universal Nuts because they were manufactured with 416 SS instead of the specified 303 SS.

    Product
    Herbst Universal Nut which is used in a Herbst Appliance A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1501-2015·2015-04-29

    SenTec Recalls V-Sign Sensor 2 Due to Premature PCO2 Unit Deterioration

    SenTec AG is voluntarily replacing V-Sign Sensor 2 units because a part of the PCO2 measuring unit deteriorates prematurely, disabling PCO2 monitoring. The recall affects 129 units in the US and 59 outside the US.

    Product
    Sentec, V-Sign Sensor 2 (REF VS-A/P/N), Reusable / Nonsterile / Waterproof, SenTec AG, CH-4106, Therwil, Switzerland. The SenTec Digital Monitoring System (SDMS) is used for continuous and non-invasive monitoring of transcutaneous carbon dioxide tension (tcPCO2), oxygen saturati
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-2012-2015·2015-04-29

    Wu Fu Yuan Sago Taro Recalled for Unapproved Red Dye

    Walong Marketing is recalling Wu Fu Yuan Sago Taro because it contains unapproved FD&C Red #2.

    Product
    Wu Fu Yuan New Sago Taro, Net Wt: 8.8oz. (250g), Manufactured by: Shanghai Yuan Zhen Food Co., Ltd, 4968-2, UPC 6927055989033
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1508-2015·2015-04-29

    Specialty Appliance Works Recalls Universal Nuts for Herbst Appliances

    Specialty Appliance Works is recalling Universal Nuts used in Herbst orthodontic appliances because they were made with 416 stainless steel instead of the specified 303 stainless steel.

    Product
    LR Telescoping Cantilever Arms (5/pk) and LL Telescoping Cantilever Arms (5/pk) A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-865-2015·2015-04-29

    Attix Pharmaceuticals Recalls Procaine Penicillin G Due to Unverified Expiry Dates

    Attix Pharmaceuticals is recalling Procaine Penicillin G active pharmaceutical ingredient because stability data does not support the printed expiry dates on repackaged lots.

    Product
    Procaine Penicillin G active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-844-2015·2015-04-29

    Attix Pharmaceuticals Recalls Piperacillin Sodium Due to Missing Stability Data

    Attix Pharmaceuticals is recalling Piperacillin Sodium active pharmaceutical ingredient because it was repackaged without data supporting the printed expiry date.

    Product
    Piperacillin Sodium active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0963-2015·2015-04-29

    Nomax Recalls Fluorescein Sodium Ophthalmic Strips for Content Uniformity Issues

    Nomax Inc is recalling Fluorescein Sodium Ophthalmic Strips because packaging degradation may affect dosage uniformity. The recall covers 62,691 cartons distributed in the US and internationally.

    Product
    Fluorescein Sodium Ophthalmic Strips USP, 1.0 mg per strip, labeled as 1) FUL-GLO, individually wrapped strips, barcode (01)00317478404019; packaged in 100-count strips per carton, (NDC 17478-404-01), UPC 3 17478 40401 9, Manufactured for: Akorn, Inc., Lake Forest, IL 60045.; and
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0964-2015·2015-04-29

    Mucinex DM Recalled for Defective Pouch Seal

    Reckitt Benckiser is recalling Mucinex DM extended-release tablets due to a defective seal on the top of the pouch.

    Product
    MUCINEX DM — MUCINEX DM (GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0962-2015·2015-04-29

    Nomax Recalls GLOSTRIPS Ophthalmic Strips for Packaging Degradation

    Nomax Inc. is recalling GLOSTRIPS ophthalmic strips because packaging degradation may affect the uniformity of the rose bengal dosage.

    Product
    GLOSTRIPS — GLOSTRIPS (ROSE BENGAL SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V249000·2015-04-28

    Spartan Recalls 2014 Utilitmaster Walk-In Vans for Driveshaft Defect

    Spartan Motors is recalling 97 model year 2014 Utilitmaster Walk-In Vans because inadequately torqued fasteners may cause the driveshaft to disconnect, increasing crash risk.

    Product
    UTILIMASTER — UTILIMASTER WALK-IN VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V251000·2015-04-28

    Ford Recalls 2015 F-150 Trucks for Missing Underbody Heat Shields

    Ford is recalling 2015 F-150 vehicles manufactured in late January 2015 because loose or missing underbody heat shields can cause fuel line degradation and increase fire risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V253000·2015-04-28

    Mastercraft Recalls 2015 Boat Trailers Due to Tongue Bolt Failure Risk

    Mastercraft is recalling 1,740 model year 2015 boat trailers because the tongue bolt may fail, allowing the trailer to disconnect from the tow vehicle and increasing crash risk.

    Product
    MASTERCRAFT — MASTERCRAFT BOAT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V250000·2015-04-28

    Ford Recalls 2013-2015 Fusion, MKZ, and Edge for Steering Bolt Corrosion

    Ford is recalling specific 2013-2015 Fusion, Lincoln MKZ, and 2015 Edge vehicles because road salt may corrode steering bolts, potentially causing a loss of power steering assist.

    Product
    LINCOLN — LINCOLN, FORD MKZ, FUSION, EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·070-2015·2015-04-27

    Skyline Provisions Recalls Beef Products Due To E. Coli O157:H7 Contamination

    Skyline Provisions is recalling 1,029 pounds of beef products contaminated with E. coli O157:H7. The recall was announced by the USDA Food Safety and Inspection Service.

    Product
    Skyline Provisions — Skyline Provisions, Inc., Recalls Beef Products Due To E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15V248000·2015-04-27

    Ford Recalls 2015 Lincoln MKZ for Excessive Parking Light Output

    Ford is recalling 21,435 2015 Lincoln MKZ vehicles because parking lights may not dim correctly when headlights are on, potentially blinding oncoming traffic.

    Product
    LINCOLN — LINCOLN MKZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V247000·2015-04-27

    Spartan Recalls Utilimaster Vans Due to Reversed Backup Camera Images

    Spartan Motors is recalling 2012-2015 Utilimaster Walk-in vans and truck bodies because the backup camera may display reversed images, increasing crash risk.

    Product
    UTILIMASTER — UTILIMASTER WALK-IN VAN, TRUCK BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·059-2015 expansion·2015-04-27

    Corn Maiden Foods Recalls Beef and Pork Products for Undeclared Soy Allergen

    Corn Maiden Foods, Inc. is expanding a recall of beef and pork products due to misbranding and an undeclared soy allergen. No adverse reactions have been reported.

    Product
    Corn Maiden Foods, Inc. — Corn Maiden Foods, Inc. Recalls Beef and Pork Products Due To Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·068-2015·2015-04-24

    Hong Ha Recalls Beef and Pork Products for Undeclared Allergens

    Hong Ha Corporation is recalling approximately 10,164 pounds of beef and pork products due to misbranding and undeclared allergens, including wheat, eggs, and milk.

    Product
    Hong Ha Corporation — Hong Ha Recalls Beef and Pork Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·15V246000·2015-04-24

    Ford Recalls Fiesta, Fusion, and MKZ Vehicles for Door Latch Defect

    Ford is recalling specific 2011-2014 Fiesta, Fusion, and MKZ vehicles because a door latch component may break, potentially allowing doors to open while driving.

    Product
    FORD — FORD, LINCOLN FIESTA, MKZ, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·069-2015·2015-04-24

    Alpine Sausage Kitchen Recalls Beef and Pork Sausages for Undeclared Soy

    Alpine Sausage Kitchen is recalling approximately 3,350 pounds of beef and pork sausage products because they contain soy, a known allergen, that is not declared on the label.

    Product
    Alpine Sausage Kitchen Recalls Beef And Pork Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·067-2015·2015-04-23

    West Liberty Foods Recalls Grilled Chicken Breast Patties Due to Plastic Contamination

    West Liberty Foods is recalling approximately 34,075 pounds of grilled chicken breast patties that may contain pieces of white plastic.

    Product
    West Liberty Foods LLC — West Liberty Foods Recalls Grilled Chicken Breast Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-1992-2015·2015-04-22

    Culinary Masters Willys Signature Spice Recalled for Undeclared Peanuts

    Gourmet Foods International is recalling Culinary Masters Willys Signature Spice because the cumin used in the product contains undeclared peanuts.

    Product
    Culinary Masters, WILLYS SIGNATURE SPICE, Net Wt. 4.4 lbs, Distributed by Atlanta Foods International, Atlanta, GA 30303.
    Category
    Food
    Distribution
    16 states
  • CriticalFDA (Food)·F-1990-2015·2015-04-22

    Culinary Masters Moroccan Seasoning Blend Recalled for Undeclared Peanuts

    Gourmet Foods International is recalling Culinary Masters Moroccan Seasoning Blend because the cumin used contains undeclared peanuts.

    Product
    Culinary Masters, MASTERS MOROCCAN SEASONING BLEND, Net Wt. 20 oz and 7 lbs. Distributed by Atlanta Foods International, Atlanta, GA 30303.
    Category
    Food
    Distribution
    16 states
  • CriticalFDA (Food)·F-1983-2015·2015-04-22

    Culinary Masters Tandoori Rub Recalled for Undeclared Peanuts

    Gourmet Foods International is recalling Culinary Masters Tandoori Rub because the cumin ingredient contains undeclared peanuts.

    Product
    Culinary Masters, SEASONING TANDOORI RUB, Net Wt. 30 oz. Distributed by Atlanta Foods International, Atlanta, GA 30303.
    Category
    Food
    Distribution
    16 states
  • CriticalFDA (Food)·F-1949-2015·2015-04-22

    Ground Cumin Recalled for Potential Peanut Contamination

    Imported Foods Resource Group is recalling 10 jars of ground cumin due to potential peanut contamination. The product was distributed to six hotels and restaurants in Massachusetts.

    Product
    Ground Cumin. 16 oz. Oz Qt Spice Jar
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1997-2015·2015-04-22

    Culinary Masters BBQ Rub Recalled for Undeclared Peanuts in Cumin

    Gourmet Foods International is recalling Culinary Masters BBQ Rub Wild Dunes because the cumin ingredient contains undeclared peanuts.

    Product
    Culinary Masters, BBQ RUB WILD DUNES, Net Wt. 7 lbs., Distributed by Atlanta Foods International, Atlanta, GA 30303.
    Category
    Food
    Distribution
    16 states
  • CriticalFDA (Food)·F-1960-2015·2015-04-22

    Trader Joe's Pita Bread Recalled for Undeclared Soy Allergen

    Middle East Bakery is recalling Trader Joe's Pocketful of Fiber Pita Bread because it may contain undeclared soy.

    Product
    Trader Joe's Pocketful of Fiber Pita Bread, UPC 00945097
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1991-2015·2015-04-22

    Culinary Masters Mustard Spice Seasoning Rub Recalled for Undeclared Peanuts

    Gourmet Foods International is recalling Culinary Masters Mustard Spice Seasoning Rub because cumin ingredients contained undeclared peanuts.

    Product
    Culinary Masters, MASTERS MUSTARD SPICE SEASONING RUB, Net Wt. 7 lbs. Distributed by Atlanta Foods International, Atlanta, GA 30303.
    Category
    Food
    Distribution
    16 states
  • CriticalFDA (Food)·F-2000-2015·2015-04-22

    Culinary Masters Bourbon Honey BBQ Rub Recalled for Undeclared Peanuts

    Gourmet Foods International is recalling Culinary Masters Bourbon Honey BBQ Rub because the cumin ingredient contains undeclared peanuts.

    Product
    Culinary Masters, BOURBON HONEY BBQ RUB, Net Wt. 7 lbs, Distributed by Atlanta Foods International, Atlanta, GA 30303.
    Category
    Food
    Distribution
    16 states

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