The Recall Desk

Archive

December 2013 recalls

1,402 recalls were announced in December 2013.

What the numbers show

Critical
354
Severe
585
High
206
Moderate
225
Low
32

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

Which agencies issued them

1201–1300 of 1402

  • HighFDA (Food)·F-0729-2014·2013-12-11

    Market Pantry Animal Cookies Recalled for Undeclared Milk and Egg

    D. F. Stauffer Biscuit Co. is recalling Market Pantry Animal Cookies due to undeclared milk and egg allergens.

    Product
    Market Pantry brand Animal Cookies, white fudge coated, in a clear plastic bear-shaped jar, net wt. 44 oz. Ingredients: enriched flour (wheat flour, malted barley flour, niacin, reduced iron, thiamin mononitrate, riboflavin, folic acid), sugar, soybean oil, high fructose corn
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-094-2014·2013-12-11

    Main Street Compounding Pharmacy Recalls Estradiol Pellets Due to Adverse Reactions

    Main Street Family Pharmacy is recalling Estradiol Pellets 31mg after receiving reports of skin abscesses linked to a different compounded product.

    Product
    Estradiol Pellets 31mg, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0454-2014·2013-12-11

    GE Centricity Web Software Recalled for Patient Safety Concerns

    GE Healthcare is recalling Centricity Web software due to an issue with rejected images that may impact patient safety.

    Product
    The GE Centricity Web; Software Version 3.0x, is intended for use under the direct supervision of a licensed healthcare practitioner. The Centricity Enterprise Web is an image and information distribution system for the clinical review of medical images and reports. The Centricit
    Category
    Medical Device
    Distribution
    13 states
  • HighFDA (Devices)·Z-0436-2014·2013-12-11

    Intuitive Surgical Recalls da Vinci Patient Side Manipulator Assemblies

    Intuitive Surgical is recalling 1,386 da Vinci Patient Side Manipulator assemblies due to friction that can cause instrument motion to stall and catch up.

    Product
    Assembly, Patient Side Manipulator on da Vinci Surgical Systems: da Vinci S Surgical System; da Vinci SI Surgical System da Vinci Si-e Surgical System; Manufactured by Intuitive Surgical Sunnyvale, CA 94086. The Intuitive Surgical Endoscopic Instrument Control System (I
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0451-2014·2013-12-11

    Abbott i-STAT PT/INR Cartridges Recalled for Potential INR Errors

    Abbott Point of Care Inc. is recalling i-STAT PT/INR cartridges because they may display incorrectly elevated INR results.

    Product
    Abbott i-STAT PT/INR cartridges Abbott Point of Care Inc., Princeton, NJ 08540 The i-Stat PT a prothrombin time test is useful for monitoring patients receiving oral anticoagulation therapy such as Coumadin or Warfarin. The cartridge is to be used with the i-Stat 1 Analyzer an
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0453-2014·2013-12-11

    Sunrise Zippie Voyage Stroller Recalled for Potential Seat Dislodgement

    Sunrise Medical is recalling Zippie Voyage strollers because a plastic latch may deform, allowing the seat to dislodge and causing the occupant to slide out.

    Product
    Sunrise Brand Zippie Voyage, Chair with Casters, Early Intervention Device (Stroller), Model: EIZ14; Product is manufactured and distributed by Sunrise Medical (US) LLC., Fresno, CA. Used by a person to move from one place to another while sitting.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0432-2014·2013-12-11

    Olympus Recalls Thunderbeat Surgical Instruments Due to Component Damage

    Olympus America Inc. is recalling Thunderbeat surgical instruments because they may crack, break, or deform during use.

    Product
    TB-0545PC: THUNDERBEAT 5 mm , 45 em, Pistol Grip TB-0535PC: THUNDERBEAT 5 mm, 35 em, Pi stol Grip TB-0545IC: THUNDERBEAT 5 mm, 45 em, In line Grip TB-0535IC: THUNDERBEAT 5 mm, 35 em, Inline Grip TB-0520IC: THUNDERBEAT 5 mm, 20 em, In line Grip TB-051 OIC: THUNDERBEAT 5 mm, I 0 em
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0698-2014·2013-12-11

    Simply D'Lish Vermont Maple Oat Cookies Recalled for Undeclared Milk Allergen

    Simply D'Lish is recalling Vermont Maple Oat Cookies because the milk allergen was not declared on the label, despite butter being listed as an ingredient.

    Product
    Vermont Maple Oat Cookie, 3-oz (85g), individually wrapped in plastic and labeled in part: Manufactured for Simply D'lish, LLC.; Aurora, IL 60504; www.simplydlish.biz
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0658-2014·2013-12-11

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

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

    Product
    Grandpas Crab Like Cheese Ball, Product Code 0 11596 55906 3, 1/5 lb
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-0700-2014·2013-12-11

    Simply D'Lish Sea Salt Chocolate Chip Cookies Recalled for Undeclared Milk

    Simply D'Lish is recalling Sea Salt Chocolate Chip Cookies because the milk allergen was not declared on the label, despite butter being listed as an ingredient.

    Product
    Sea Salt Chocolate Chip Cookie, 3-oz (85g), individually wrapped in plastic and labeled in part: Manufactured for Simply D'lish, LLC.; Aurora, IL 60504; www.simplydlish.biz
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0699-2014·2013-12-11

    Simply D'Lish Peanut Butter Chocolate Chip Cookies Recalled for Undeclared Milk

    Simply D'Lish is recalling peanut butter chocolate chip cookies because the milk allergen was not declared on the label, despite butter being listed as an ingredient.

    Product
    Peanut Butter Chocolate Chip Cookie,3-oz (85g), individually wrapped in plastic and labeled in part: Manufactured for Simply D'lish, LLC.; Aurora, IL 60504; www.simplydlish.biz
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0696-2014·2013-12-11

    Simply D'Lish Caramel Sea Salt Chocolate Chip Cookies Recalled for Undeclared Milk

    Simply D'Lish is recalling Caramel Sea Salt Chocolate Chip Cookies because the milk allergen was not declared on the label.

    Product
    Caramel Sea Salt Chocolate Chip Cookie, 3-oz (85g), individually wrapped in plastic wrapper and labeled in part: Manufactured for Simply D'lish, LLC.; Aurora, IL 60504; www.simplydlish.biz
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0675-2014·2013-12-11

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

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

    Product
    Grandpas Fresh Salsa, Product Code 5912, 1/5 lb; Grandpas Fresh Salsa, Product Code 5913, 19 4/5 lb; Roundy's Fresh Salsa Product Code 0 11596 06117 7, 12/15 oz
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-0455-2014·2013-12-11

    Synthes Zero-P VA Implant Recalled for Potential Screw Back-Out Risk

    Synthes USA is recalling specific Zero-P VA implants because a screw could back out if the blocking mechanism is not visually confirmed to cover the screw head.

    Product
    Synthes Zero-P VA Implant 7 MM Height Parallel Sterile The Synthes Zero-P VA Implant 7 MM Height Parallel Sterile is a stand alone anterior cervical interbody fusion device indicated for use in skeletally mature patients with degenerative disc disease (DDD) with accompanying r
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0440-2014·2013-12-11

    Boston Scientific Recalls Navigator HD Ureteral Access Sheath Sets

    Boston Scientific is recalling 274 units of Navigator HD Ureteral Access Sheath Sets because the dilator tip may separate from the body.

    Product
    Navigator HD l3F/15F x 28 cm Ureteral Access Sheath Set Product No M0062502270, RDF Catalog No 250-227, Sterile. Indicated for use in endoscopic procedures to facilitate the passage of endoscopes, urological instruments and for the injection of fluids into the urinary tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0441-2014·2013-12-11

    Boston Scientific Recalls Navigator HD Ureteral Access Sheath Sets

    Boston Scientific is recalling Navigator HD Ureteral Access Sheath Sets because the dilator tip may separate from the body.

    Product
    Navigator HD l3F/15F x 36cm Ureteral Access Sheath Set Product No M0062502280, RDF Catalog No 250-228, Sterile. Indicated for use in endoscopic procedures to facilitate the passage of endoscopes, urological instruments and for the injection of fluids into the urinary tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0712-2014·2013-12-11

    Ocean State Jobbers Recalls Mediterranean Olives Due to Storage Labeling Error

    Ocean State Jobbers is recalling 8,052 units of Mediterranean Olives: Green Stuffed because the product was stored at room temperature instead of being refrigerated as required by the label.

    Product
    Mediterranean Olives: Green Stuffed, produced by Bel Frantoio and packaged in 34-oz. plastic containers. Imported from Italy
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Food)·F-0727-2014·2013-12-11

    Oma's Choice Habanero Garlic Recalled for Lack of Process Authority Evaluation

    Oma's Choice Inc is recalling 28 cases of Habanero Garlic because the products were not submitted to a process authority for evaluation.

    Product
    Oma's Choice, Habanero Garlic, Net Wt. 16 oz., Made Espcially For Oma's Choice, 4042 F.M. 3171 Schulenburg, TX 78956.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1344-2012·2013-12-11

    Evergreen Farm Pear Juice Gochujang Recalled for Incorrect Labeling

    Evergreen Orchard Farm, LLC is recalling Pear Juice Gochujang due to incorrect labeling, product descriptions, and formulations.

    Product
    Evergreen Farm Pear Juice Gochujang (Hot Peppeer Paste). Net Wt 70 ounce (4.4 LBS) glass jars. 1023 Yardville Allentown Road, Hamilton NJ 08620. Product of USA. UPC # 89076726177.
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0449-2014·2013-12-11

    Smith & Nephew Recalls Genesis II Knee Inserts Due to Seal Defect

    Smith & Nephew is recalling 8 units of Genesis II mobile bearing articular inserts because the Tyvek lid may not be adequately sealed.

    Product
    GENESIS(R) II, MOBILE BEARING ARTICULAR INSERT RIGHT, SIZE 5, 9 MM QTY: (1), REF 71621509, STERILE EO, Smith & Nephew, Inc. Memphis, TN 38116 USA Orthopedic
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0434-2014·2013-12-11

    Advanced Sterilization Products Recalls SteriTite Containers Due to Sterility Assurance Concerns

    Advanced Sterilization Products is recalling SteriTite containers because data does not consistently show that the required sterility assurance level is achieved during testing.

    Product
    STERITITE Containers: STERITITE Container Kit, 1/4 size, 3" high, product code: 13902; STERITITE Mini Mid Size, 3" high, product code: 13903; STERITITE Container Kit, 1/2 size, 4" high, product code: 13904; STERITITE Container Kit, 3/4 size, 4" high, product code: 13905; STERITIT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0709-2014·2013-12-11

    Gold Medal Caramel Dip Recalled for Insanitary Manufacturing Conditions

    Gold Medal Products is recalling Caramel Dip in plastic containers because it was manufactured under insanitary conditions. The product was distributed in 14 US states and Canada.

    Product
    Product #4124: Caramel dip in plastic containers
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Food)·F-0695-2014·2013-12-11

    N4H Research Easy Protein Recalled for Mold Contamination in Texas

    N4H Research LLC is voluntarily recalling 139 bottles of Easy Protein in Texas due to mold contamination. The recall was initiated in 2012 and terminated in 2015.

    Product
    N4H RESEARCH Easy Protein 20 GRAMS OF PROTEIN PER SERVING NEUTRAL FLAVOR ALL NATURAL GLUTEN FREE 16 FL OZ Ingredients: Pure deionized water, Actinase [patent pending blend of enzymatically hydrolyzed (predigested) collagenic protein isolate, whey protein, isolate (milk) and cas
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0717-2014·2013-12-11

    Ocean State Jobbers Recalls Mediterranean Olives Due to Storage Labeling Error

    Ocean State Jobbers is recalling Mediterranean Olives: Cracked Cerignole because the product was stored at room temperature instead of being refrigerated as required by the label.

    Product
    Mediterranean Olives: Cracked Cerignole, produced by Bel Frantoio and packaged in 34-oz. plastic containers. Imported from Italy
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0435-2014·2013-12-11

    CareFusion Recalls VersaSafe Extension Sets Due to Adhesive Defect

    CareFusion is recalling VersaSafe Extension Sets because excessive adhesive may prevent the male spin collar from operating as intended.

    Product
    VersaSafe Extension Set, Model No. 21000M-007
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0716-2014·2013-12-11

    Ocean State Jobbers Recalls Mediterranean Olives Stored at Room Temperature

    Ocean State Jobbers is recalling Mediterranean Olives: Dry Morrocan because they were stored at room temperature instead of being refrigerated as required by the label.

    Product
    Mediterranean Olives: Dry Morrocan, produced by Bel Frantoio and packaged in 34-oz. plastic containers. Imported from Italy
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Food)·F-0718-2014·2013-12-11

    Ocean State Jobbers Recalls Mediterranean Olives Due to Improper Storage

    Ocean State Jobbers is recalling 1,404 units of Mediterranean Olives: French Picholine because they were stored at room temperature instead of refrigerated.

    Product
    Mediterranean Olives: French Picholine, produced by Bel Frantoio and packaged in 34-oz. plastic containers. Imported from Italy
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Food)·F-0719-2014·2013-12-11

    Ocean State Jobbers Recalls Kalamata Olives Due to Improper Storage

    Ocean State Jobbers is recalling 6,216 units of Kalamata olives because they were stored at room temperature instead of refrigerated.

    Product
    Mediterranean Olives: Kalamata, produced by Bel Frantoio and packaged in 34-oz. plastic containers. Imported from Italy
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Food)·F-0694-2014·2013-12-11

    Borinquen Natural Recalls HCG Premium Energy Drops for False Health Claims

    Borinquen Natural is recalling HCG Premium Energy Hormone-Free Drops because the company's website made false claims that the product prevents various diseases.

    Product
    HCG Premium Energy Hormone-Free Drops with B12, B6 & Yohimbine, 60 ml
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0439-2014·2013-12-11

    Varian Medical Systems Recalls C-Series Linear Accelerators for Software Correction

    Varian Medical Systems is recalling 3,809 C-Series linear accelerators to install a software solution that corrects a previous issue.

    Product
    C-Series: Clinac, Trilogy, Trilogy Tx. , Novalis high energy linear accelerators and UNIQUE single energy linear accelerator; Versions 7, 8 and 9. The UNIQUE is not sold in the US. Product Usage: The Varian High Energy Linear Accelerator is indicated for stereotactic radiosu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0708-2014·2013-12-11

    Ocean State Jobbers Recalls Mediterranean Olives Due to Improper Storage

    Ocean State Jobbers is recalling Mediterranean Olives: Calcidica Sweet because they were stored at room temperature instead of being refrigerated as required by the label.

    Product
    Mediterranean Olives: Calcidica Sweet, produced by Bel Frantoio and packaged in 34-oz. plastic containers. Imported from Italy
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0430-2014·2013-12-11

    Siemens Dimension Vista Diagnostic Vials Recalled for Volume Error

    Siemens is recalling Dimension Vista 500 and 1500 reloaded vials because they may incorrectly reset to full volume, potentially affecting diagnostic accuracy.

    Product
    Dimension Vista(R) 500 and Dimension Vista(R) 1500 - Reloaded Vista Vials - limited to systems using software versions 3.4 and 3.5.1. Diagnostic device intended to determine a variety of analytes in human body fluids.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0445-2014·2013-12-11

    Smith & Nephew Recalls Genesis II Knee Inserts Due to Seal Defect

    Smith & Nephew is recalling 45 units of Genesis II knee inserts because the Tyvek lid may not be adequately sealed, potentially compromising sterility.

    Product
    GENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT, SIZE 3-4, 13 MM QTY: (1), REF 71420820, STERILE EO, Smith & Nephew, Inc. Memphis, TN 38116 USA Orthopedic
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-0720-2014·2013-12-11

    Ocean State Jobbers Recalls Mediterranean Olives Due to Improper Storage

    Ocean State Jobbers is recalling 5,448 units of Mediterranean Olives: Large because they were stored at room temperature instead of refrigerated.

    Product
    Mediterranean Olives: Large, produced by Bel Frantoio and packaged in 34-oz. plastic containers. Imported from Italy
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Food)·F-1342-2012·2013-12-11

    Evergreen Orchard Farm Recalls Korean Grape Juice for Incorrect Labeling

    Evergreen Orchard Farm is recalling Korean Grape Juice in 110 mL pouches due to incorrect labeling, product descriptions, and formulations.

    Product
    Korean Grape Juice, 110 mL metal foil pouch single service container. Made by Evergreen Orchard Farm, 1023 Yardville Allentown Road, Hamilton, NJ 08620 Product of USA. UPC #8907672547.
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0429-2014·2013-12-11

    Synthes Soft Tissue Retractor Recalled for Locking Nut Malfunction

    Synthes USA HQ, Inc. is recalling 374 units of the Small Extendible Soft Tissue Retractor due to a locking nut malfunction.

    Product
    Synthes Soft Tissue Retractor Small Extendible. Offset blade facilitates easy preparation of the epipereosteal cavity for percutaneous plate insertion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0714-2014·2013-12-11

    Ocean State Jobbers Recalls Mediterranean Olives Due to Improper Storage

    Ocean State Jobbers is recalling Mediterranean Olives: Gaeta White because the product was stored at room temperature instead of being refrigerated.

    Product
    Mediterranean Olives: Gaeta White, produced by Bel Frantoio and packaged in 34-oz. plastic containers. Imported from Italy
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0450-2014·2013-12-11

    CareFusion Recalls SmartSite Infusion Sets Due to Tubing Assembly Error

    CareFusion is recalling 480 units of SmartSite Low Sorbing Infusion Sets because they were not assembled with low-sorbing tubing.

    Product
    SmartSite Low Sorbing Infusion Set with Texium Close Male Luer, Model No. 24301-0007T The SmartSite Low Sorbing Infusion Sets with Texium Male Luer are used to administer fluid and medications through a needle or catheter inserted into the patient's artery or vein.
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Food)·F-0725-2014·2013-12-11

    Oma's Choice Dilled Garlic Recalled for Lack of Process Authority Evaluation

    Oma's Choice Inc is recalling 28 cases of Dilled Garlic because the products were not submitted to a process authority for evaluation.

    Product
    Oma's Choice, Dilled Garlic, Net. Wt. 16 oz, Made Espcially For Oma's Choice, 4042 F.M. 3171 Schulenburg, TX 78956.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0444-2014·2013-12-11

    Smith & Nephew Recalls Genesis II Knee Inserts Due to Seal Defect

    Smith & Nephew is recalling 16 Genesis II knee inserts because the Tyvek lid may not be adequately sealed, potentially compromising sterility.

    Product
    GENESIS(R) II, POSTERIOR STABILIZED ARTICULAR INSERT, SIZE 1-2, 13 MM QTY: (1), REF 71420806, STERILE EO, Smith & Nephew, Inc. Memphis, TN 38116 USA Orthopedic
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-1341-2012·2013-12-11

    Evergreen Orchard Farm Recalls Korean Pear Juice for Incorrect Labeling

    Evergreen Orchard Farm is recalling Korean Pear Juice in 120 mL pouches due to incorrect labeling, product descriptions, and formulations.

    Product
    Korean Pear Juice in 120 mL metal foil pouch single service container. Made by Evergreen Orchard Farm, 1023 Yardville Allentown Road, Hamilton, NJ 08620. Product of USA. UPC# 809080300084.
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Food)·F-0724-2014·2013-12-11

    Oma's Choice Baby Dill Pickles Recalled for Lack of Process Authority Evaluation

    Oma's Choice Inc is recalling Baby Dill Pickles because the products were not submitted to a process authority for evaluation.

    Product
    Oma's Choice, Baby Dill Pickles, Net Wt. 16.oz., Made Espcially For Oma's Choice, 4042 F.M. 3171 Schulenburg, TX 78956.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0447-2014·2013-12-11

    Smith & Nephew Recalls Genesis II Knee Inserts Due to Sealing Defect

    Smith & Nephew is recalling 32 Genesis II knee inserts because the Tyvek lid may not be adequately sealed, potentially compromising sterility.

    Product
    GENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT, SIZE 5-6, 9 MM QTY: (1), REF 71421515, STERILE EO, Smith & Nephew, Inc. Memphis, TN 38116 USA Orthopedic
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-0713-2014·2013-12-11

    Ocean State Jobbers Recalls Mediterranean Olives Due to Improper Storage

    Ocean State Jobbers is recalling 4,296 units of Mediterranean Olives because they were stored at room temperature instead of being refrigerated.

    Product
    Mediterranean Olives: Small, produced by Bel Frantoio and packaged in 34-oz. plastic containers. Imported from Italy
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Food)·F-0722-2014·2013-12-11

    Sweetwater Recalls Refreshe Lime Electrolyte Water Due to Coliforms

    The Sweetwater Co. is recalling Refreshe Lime Naturally Flavored Electrolyte Water due to elevated non-fecal total Coliforms.

    Product
    Refreshe Lime Naturally Flavored Electrolyte Water, 12 bottles per cases, 1 L per bottle, sold under Safeway brand. The UPC 0 21130 24208 5.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-324-2014·2013-12-11

    Badger Baby Sunscreen Recalled for Microbial Contamination

    W.S. Badger Company Inc. is recalling specific lots of Badger Baby and Kids Sunscreen Lotion due to microbial contamination.

    Product
    Badger Baby Broad Spectrum SPF 30 Zinc Oxide Sunscreen Lotion Chamomile & Calendula, 4fFl.oz Tube, UPC code: 634084490091 (US) UPC Code: 634084490114 (Canada)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0693-2014·2013-12-11

    Borinquen Natural Recalls HCG Premium Cleanse Drops for False Health Claims

    Borinquen Natural is recalling HCG Premium Cleanse Hormone-Free Drops because the company's website made false claims that the product prevents serious diseases.

    Product
    HCG Premium Cleanse Hormone-Free Drops with Acai Berry & Raspberry Ketone, 60 ml
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0711-2014·2013-12-11

    Ocean State Jobbers Recalls Mediterranean Black Olives for Storage Label Violation

    Ocean State Jobbers is recalling 8,172 units of Mediterranean Black Olives because they were stored at room temperature instead of being refrigerated as required by the label.

    Product
    Mediterranean Olives: Black, produced by Bel Frantoio and packaged in 34-oz. plastic containers. Imported from Italy
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0431-2014·2013-12-11

    Philips Easy Diagnost Eleva Fluoroscopic Software Recall

    Philips Medical Systems is recalling 19 Easy Diagnost Eleva devices because they were delivered with outdated application software.

    Product
    Easy Diagnost Eleva Universal Fluoroscopic applications
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1343-2012·2013-12-11

    Evergreen Farm Soybean Paste Recalled for Incorrect Labeling and Formulation

    Evergreen Orchard Farm, LLC is recalling Doen Jang (Soybean Paste) because the product displays incorrect labeling, product descriptions, and formulations.

    Product
    Evergreen Farm Doen Jang (Soybean Paste). Net Wt, 70 ounces (4.4 LBS) in glass jars. 1023 Yardville Allentown Road, Hamilton NJ 08620. Product of USA. UPC# 89076725873
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Food)·F-0726-2014·2013-12-11

    Oma's Choice Recalls Pickled Quail Eggs Due to Process Authority Failure

    Oma's Choice Inc is recalling pickled quail eggs because the products were not submitted to a process authority for evaluation.

    Product
    Oma's Choice, Pickled Quail Eggs, Net. Wt. 16 oz., Made Espcially For Oma's Choice, 4042 F.M. 3171 Schulenburg, TX 78956.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0443-2014·2013-12-11

    Cincinnati Sub-Zero Recalls Blanketrol III Data Export Software Version 1.10

    Cincinnati Sub-Zero Products Inc is recalling 12 units of Blanketrol III Data Export Software Version 1.10 because the wrong software version was released to a customer.

    Product
    Blanketrol III Data Export Software Version 1.10 The Blanketrol III Data Export Software is intended for use in the electronic transfer of medical device data from the Blanketrol III to a computer, without controlling or altering the function or parameters of the Blanketrol II
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Food)·F-0723-2014·2013-12-11

    Sweetwater Recalls Refreshe Mixed Berry Electrolyte Water Due to Coliforms

    The Sweetwater Co. is recalling Refreshe Mixed Berry Electrolyte Water sold in California and Oregon due to elevated non-fecal total Coliforms.

    Product
    Refreshe Mixed Berry Naturally Flavored Electrolyte Water, 12 bottles per cases, 1 L per bottle, sold under Safeway brand. The UPC 0 21130 24209 2.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0715-2014·2013-12-11

    Ocean State Jobbers Recalls Mediterranean Olives Due to Improper Storage

    Ocean State Jobbers is recalling 4,536 units of Mediterranean Olives: Gaeta Black because they were stored at room temperature instead of refrigerated.

    Product
    Mediterranean Olives: Gaeta Black, produced by Bel Frantoio and packaged in 34-oz. plastic containers. Imported from Italy
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0446-2014·2013-12-11

    Smith & Nephew Recalls Genesis II Knee Inserts Due to Seal Defect

    Smith & Nephew is recalling 80 Genesis II knee inserts because the Tyvek lid may not be adequately sealed, potentially compromising sterility.

    Product
    GENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT, SIZE 3-4, 9 MM QTY: (1), REF 71421508, STERILE EO, Smith & Nephew, Inc. Memphis, TN 38116 USA Orthopedic
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0448-2014·2013-12-11

    Smith & Nephew Recalls Genesis II Knee Inserts Due to Seal Defect

    Smith & Nephew is recalling 46 Genesis II knee inserts because the Tyvek lid may not be adequately sealed, potentially compromising sterility.

    Product
    GENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT, SIZE 5-6, 11 MM QTY: (1), REF 71421516, STERILE EO, Smith & Nephew, Inc. Memphis, TN 38116 USA Orthopedic
    Category
    Medical Device
    Distribution
    1 state
  • HighCPSC·14047·2013-12-10

    efco Gas Trimmers Recalled by CPSC Due to Fire Hazard

    Emak USA is recalling efco gas trimmers because the engine muffler can break and cause a fire. Consumers should stop using them and return them for a free repair.

    Product
    efco brand Gas Trimmers from Emak USA
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14048·2013-12-10

    PackTite Recalls Bed Bug Heating Units Due to Fire Hazard

    PackTite is recalling approximately 9,000 bed bug heating units because they can overheat, melt, and cause fires. No injuries have been reported.

    Product
    PackTite™ Heating Units for Bed Bug Control
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14045·2013-12-10

    Exmark Recalls Commercial Walk-Behind Mowers Due to Blade Injury Hazard

    Exmark is recalling 2013 Commercial 30-inch Walk-Behind Mowers because the blade can break and injure users. Consumers should stop using the mowers and contact Exmark for a free repair.

    Product
    Commercial Walk-Behind Mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V637000·2013-12-09

    Marathon Recalls 2006-2013 Trailers Due to Door Lock Jamming Risk

    Marathon Homes is recalling 2006-2013 towable and fifth wheel travel trailers because a door lock defect may jam the deadbolt, potentially trapping occupants inside.

    Product
    MARATHON — MARATHON TOWABLE TRAILER/5TH WHEEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14044·2013-12-09

    Linear Recalls PERS Transmitters Due to Battery Signal Failure

    Linear is recalling about 48,000 Personal Emergency Reporting System transmitters because battery clips can corrode, causing the devices to fail without warning.

    Product
    Personal Emergency Reporting System (PERS) Transmitters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V652000·2013-12-09

    Skyline Recalls 2006-2013 Trailers Due to Door Lock Jamming Risk

    Skyline is recalling 2006-2013 travel and fifth-wheel trailers because a door lock defect could jam the deadbolt, potentially trapping occupants inside.

    Product
    SKYLINE — SKYLINE SKYCAT, WEEKENDER, NOMAD, MOUNTAINVIEW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13E069000·2013-12-06

    Omix Ada Recalls Jeep Replacement Brake Hoses Due to Leak Risk

    Omix Ada is recalling certain front and rear braided stainless steel replacement brake hoses for modified Jeep vehicles because they may leak fluid or rupture.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V610000·2013-12-06

    Chrysler Recalls 2013 Vehicles for Transmission Output Shaft Fracture Risk

    Chrysler is recalling 2013 Chrysler 300, Dodge Charger, and Ram 1500 vehicles because a transmission output shaft may fracture, potentially causing loss of power or the vehicle rolling away.

    Product
    DODGE — DODGE, CHRYSLER, RAM CHARGER, 300, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V611000·2013-12-06

    Covered Wagon Trailers Recalling Cargo Trailers Due to Door Lock Defect

    Covered Wagon Trailers is recalling 2006-2013 cargo trailers because a door lock defect could jam the deadbolt, potentially trapping occupants inside.

    Product
    COVERED WAGON TRAILERS — COVERED WAGON TRAILERS CARGO TRAILERS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V613000·2013-12-06

    Spartan Emergency Vehicles Recalled for Defective Seat Belt Buckles

    Spartan Motors is recalling specific emergency vehicles because seat belt buckles may fail to release, potentially hindering egress during an emergency.

    Product
    SPARTAN — SPARTAN GLADIATOR, METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V612000·2013-12-05

    Kenworth Recalls 2014 Trucks Due to Stop/Tail/Turn Lamp Housing Defect

    PACCAR is recalling 5,087 model year 2014 Kenworth trucks because the stop/tail/turn lamp housing can shrink, allowing the bulb to fall out and fail to illuminate.

    Product
    KENWORTH — KENWORTH T170, T270, T700, T470
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-021-2014·2013-12-04

    Jack Rabbit Herbal Supplement Recalled for Undeclared Prescription Ingredients

    Jack Rabbit, Inc. is recalling its J.R. Jack Rabbit All Natural Herbal Supplement because FDA testing found undeclared sildenafil and tadalafil.

    Product
    J.R. Jack Rabbit All Natural Herbal Supplement, One tablet can last 24-72 hours, 4-count tablets per blister pack, Order at: www.jackrabbitfourpack.com, Jack Rabbit Inc., 4355 Dow Road, Melbourne, FL 32934
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0362-2014·2013-12-04

    Plum Organics Tots Blueberry Oats & Quinoa Recalled for Contamination

    Plum Inc is recalling specific lots of Plum Organics Tots Blueberry Oats & Quinoa due to a manufacturing defect that led to post-process contamination.

    Product
    Plum Organics Tots Blueberry Oats & Quinoa Morning Mish Mash - 12.79 oz. box. Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT. DISTRIBUTED B
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0365-2014·2013-12-04

    Plum Organics Baby Food Recalled for Manufacturing Defect and Contamination

    Plum Inc is recalling specific lots of Plum Organics Blueberry, Pear and Purple Carrot Organic Baby Food due to a manufacturing defect leading to post-process contamination.

    Product
    Plum Organics Blueberry, Pear and Purple Carrot Organic Baby Food, 4 oz. pouch.. Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT. DISTRIBU
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0373-2014·2013-12-04

    Plum Organics Baby Food Recalled for Manufacturing Defect

    Plum Inc is recalling specific lots of Plum Organics Blueberry, Parsnip & Buckwheat Organic Baby Food due to a manufacturing defect that led to post-process contamination.

    Product
    Plum Organics Blueberry, Parsnip & Buckwheat Organic Baby Food- 3.5 oz. Pouch . Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT. DISTRIBUTE
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0376-2014·2013-12-04

    Plum Organics Baby Food Recalled for Manufacturing Defect

    Plum Inc is recalling specific lots of Plum Organics Mango, Carrot & Greek Yogurt Baby Food due to a manufacturing defect that led to post-process contamination.

    Product
    Plum Organics Mango, Carrot & Greek Yogurt Organics Baby Food- 3.5 oz. Pouch Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT. DISTRIBUTED
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0346-2014·2013-12-04

    Pacific Nutritionals Recalls Superior Digestion Dietary Supplement Due to Contamination

    Pacific Nutritionals is recalling Superior Digestion dietary supplements contaminated with Chloramphenicol. The products were distributed in Florida and Canada.

    Product
    -Superior Digestion, 60 capsules per bottle, is dietary supplement and sold under Purelife Naturals brand. The UPC Code 6 31257 17509 0. -Superior Digestion, Dietary Supplement, Bulk Case, NO UPC. The retail 60 count bottle is labeled in parts: "***Superior Digestion***p
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0371-2014·2013-12-04

    Plum Kids Tropical Fruit Mashups Recalled for Contamination Risk

    Plum Inc is recalling Tropical Fruit Mashups due to a manufacturing defect that may have caused post-process contamination.

    Product
    Plum Kids Tropical Fruit Mashups, 12.69 oz. box. Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT. DISTRIBUTED BY: NEST COLLECTIVE, INC. EM
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0423-2014·2013-12-04

    DePuy Orthopaedics Recalls HP M.B.T. Keel Punch Knee Instruments

    DePuy Orthopaedics is voluntarily recalling HP M.B.T. Keel Punch Knee Instruments because tabs on the connection end may fracture and remain in the patient.

    Product
    SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 4-7 HP M.B.T. Keel Punch Knee Instrument is used to prepare the proximal tibial canal geometry to accept the final or definitive tibial tray used during total knee arthroplasty.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0345-2014·2013-12-04

    Renew Life ParaZYME Dietary Supplement Recalled for Chloramphenicol Contamination

    Pacific Nutritionals is recalling Renew Life ParaZYME dietary supplements because the ingredients are contaminated with Chloramphenicol.

    Product
    ParaZYME, 90 capsules per bottle, is dietary supplement and sold under Renew Life brand. The UPC Code 6 31257 30990 7. The product is labeled in parts: "***PARAZYME***renew LIFE***The Digestive Care Company***90 Vegetable Capsules***Distributed by: ReNew Life Formulas***Palm
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0355-2014·2013-12-04

    Plum Organics Baby Food Recalled for Post-Process Contamination

    Plum Inc is recalling Zucchini, Banana & Amaranth Organic Baby Food due to a manufacturing defect that led to post-process contamination.

    Product
    Plum Organics Zucchini, Banana & Amaranth Organic Baby Food; 3.5 oz. Pouch; Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT. DISTRIBUTED BY:
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0347-2014·2013-12-04

    Renew Life DigestMORE Food Supplements Recalled for Chloramphenicol Contamination

    Pacific Nutritionals is recalling Renew Life DigestMORE and DigestMORE Ultra food supplements because they are contaminated with Chloramphenicol.

    Product
    -DigestMORE, 90 capsules per bottle, Food Supplement is sold under Renew Life brand. The UPC Code 6 31257 35000 8. -DigestMORE Ultra, 60 capsules per bottle, Food Supplement is sold under Renew Life brand. The UPC Code 6 31257 35001 5. The DigestMORE product is labeled i
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0374-2014·2013-12-04

    Plum Organics Baby Food Recalled for Post-Process Contamination

    Plum Inc is recalling specific lots of Plum Organics Pumpkin, Dates, Oats & Chia Organic Baby Food due to a manufacturing defect that led to post-process contamination.

    Product
    Plum Organics Pumpkin, Dates, Oats & Chia Organic Baby Food- 3.5 oz. Pouch Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT. DISTRIBUTED BY
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0415-2014·2013-12-04

    DePuy Recalls HP M.B.T. Keel Punch Knee Instruments Due to Fracture Risk

    DePuy Orthopaedics is voluntarily recalling HP M.B.T. Keel Punch Knee Instruments because tabs on the connection end may fracture and be left in the patient.

    Product
    SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH NONCEMENTED Size 1-1.5 HP M.B.T. Keel Punch Knee Instrument is used to prepare the proximal tibial canal geometry to accept the final or definitive tibial tray used during total knee arthroplasty.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0382-2014·2013-12-04

    Nexgen Pharma Recalls Woman's Once Daily Vitamin Tablets Due to Chloramphenicol Contamination

    Nexgen Pharma is recalling one lot of Woman's Once Daily vitamin tablets because they were contaminated with the antibiotic Chloramphenicol.

    Product
    PCC, Rebecca's Natural Food, Sprouts Famous Market, Ritzman Pharmacy, Earth Fare, Hartig Drug, Viroqua Food, Ramona Fitness Center, Independent Choice (Health Trail Natural Foods-The Crunchy Grocer), Jimbo's, Outpost Natural Foods BRANDS- Woman's Once Daily Tablets - A dietary Su
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0367-2014·2013-12-04

    Plum Organics Baby Food Recalled for Post-Process Contamination

    Plum Inc is recalling Pear and Mango Organic Baby Food due to a manufacturing defect that led to post-process contamination.

    Product
    Plum Organics Pear and Mango Organic Baby Food, 4.0 oz. pouch.. Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT. DISTRIBUTED BY: NEST CO
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0358-2014·2013-12-04

    Plum Organics Tots Berry, Banana, Beet Yogurt Mish Mash Recalled for Contamination

    Plum Inc is recalling specific lots of Plum Organics Tots Berry, Banana, Beet Yogurt Mish Mash due to a manufacturing defect that led to post-process contamination.

    Product
    Plum Organics Tots Berry, Banana, Beet Yogurt Mish Mash; 3.17 oz. Pouch; also in 12.69 oz. box. Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0360-2014·2013-12-04

    Plum Organics Baby Food Recalled for Post-Process Contamination

    Plum Inc. is recalling Green Bean, Pear & Greek Yogurt organic baby food due to a manufacturing defect leading to post-process contamination.

    Product
    Plum Organics Green Bean, Pear & Greek Yogurt Organic Baby Food, 4 oz. pouch. Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT. DISTRIBUTED BY
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0421-2014·2013-12-04

    DePuy Orthopaedics Recalls HP M.B.T. Keel Punch Knee Instruments

    DePuy Orthopaedics is voluntarily recalling HP M.B.T. Keel Punch Knee Instruments because tabs on the connection end may fracture and remain in the patient.

    Product
    SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 1-1.5 HP M.B.T. Keel Punch Knee Instrument is used to prepare the proximal tibial canal geometry to accept the final or definitive tibial tray used during total knee arthroplasty.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0417-2014·2013-12-04

    DePuy Orthopaedics Recalls HP M.B.T. Keel Punch Knee Instruments

    DePuy Orthopaedics is voluntarily recalling HP M.B.T. Keel Punch Knee Instruments because tabs on the connection end may fracture and remain in the patient.

    Product
    SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH NONCEMENTED Size 4-7 HP M.B.T. Keel Punch Knee Instrument is used to prepare the proximal tibial canal geometry to accept the final or definitive tibial tray used during total knee arthroplasty.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0413-2014·2013-12-04

    DePuy Orthopaedics Recalls HP M.B.T. Keel Punch Knee Instruments

    DePuy Orthopaedics is voluntarily recalling HP M.B.T. Keel Punch Knee Instruments because tabs on the connection end may fracture and remain in the patient.

    Product
    SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH CEMENTED Size 2-3 HP M.B.T. Keel Punch Knee Instrument is used to prepare the proximal tibial canal geometry to accept the final or definitive tibial tray used during total knee arthroplasty
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0351-2014·2013-12-04

    Plum Organics Broccoli & Apple Baby Food Recalled for Contamination

    Plum Inc is recalling Broccoli & Apple Organic Baby Food due to a manufacturing defect that led to post-process contamination.

    Product
    Plum Organics Broccoli & Apple Organic Baby Food, 4 oz. pouch; Flexible pouch with Re-sealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT. DISTRIBUTED BY: NEST COLLECTI
    Category
    Food
    Distribution
    Distributed nationwide

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