The Recall Desk

Archive

July 2015 recalls

1,183 recalls were announced in July 2015.

What the numbers show

Critical
342
Severe
255
High
333
Moderate
232
Low
21

Of the 1,183 recalls this month scored against our rubric, 29% are Critical, 22% are Severe.

Which agencies issued them

301–400 of 1183

  • SevereFDA (Drugs)·D-1089-2015·2015-07-15

    Teva Recalls Adrucil Fluorouracil Injection Due to Particulate Matter

    Teva Pharmaceuticals is recalling Adrucil (fluorouracil injection) vials due to the presence of black particulate matter, including silicone rubber and drug crystals.

    Product
    Adrucil (fluorouracil injection, USP) Pharmacy Bulk Package Not for Direct Infusion, 5 g/100 mL (50 mg/mL), For Intravenous Use Only, Rx Only, Teva Parenteral Medicines, Inc., Irvine, CA 92618, NDC 0703-3019-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2820-2015·2015-07-15

    Southern Style Spices Recalls Ground Cumin for Peanut Protein

    Southern Style Spices is recalling 775 lbs of ground cumin distributed in Texas because it may contain peanut protein.

    Product
    Cumin, Ground NET WT. 50 LBS. DISTRIBUTED BY: SOUTHERN STYLE SPICES PO BOX 20 MANOR, TX 78653 PHONE: (512)272-5621
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-2811-2015·2015-07-15

    Boba Direct Vanilla Bubble Tea Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling vanilla bubble tea powder sold in foil bags due to undeclared allergens. The product was distributed in five states.

    Product
    Foil bags containing 2.2 lbs. each of vanilla flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2794-2015·2015-07-15

    Boba Direct Blueberry Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling blueberry flavored powder due to undeclared allergens. The product was distributed in five US states.

    Product
    Foil bags containing 2.2 lbs. each of blueberry flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2835-2015·2015-07-15

    Hazelwood's Smoky Sweet Salsa Recalled for Potential Peanut Contamination

    Paradigm Foodworks is recalling Hazelwood's Smoky Sweet Salsa due to potential peanut protein contamination. The product was distributed in four US states and Ontario, Canada.

    Product
    Smoky Sweet Salsa, All Natural Medium, Hazelwood's brand, Net Wt. 16 oz (453 g), UPC 8-52707-00200-5
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2833-2015·2015-07-15

    D.A.M. Spicy Maria Salsa Recalled for Potential Peanut Contamination

    Paradigm Foodworks is recalling D.A.M. brand Spicy Maria Salsa due to potential peanut protein contamination. Consumers should check their pantry for the specific lot code.

    Product
    Spicy Maria Salsa, D.A.M. brand, Net Wt. 16 oz (453 g), UPC 1-87283-00003-0
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2825-2015·2015-07-15

    Soog Head Hot Pineapple Smash Salsa Recalled for Peanut Contamination

    Paradigm Foodworks is recalling Soog Head Hot Pineapple Smash Salsa due to potential contamination with peanut protein.

    Product
    Hot Pineapple Smash Salsa, Soog Head brand, Net Wt. 16 oz. (453 g), UPC 6-26570-62022-8
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2836-2015·2015-07-15

    Hungry Dragon Stir Fry Marinade Recalled for Peanut Contamination

    Paradigm Foodworks is recalling The Hungry Dragon Original Flavor Stir Fry Marinade BBQ Sauce due to potential peanut protein contamination.

    Product
    Original Flavor Stir Fry Marinade BBQ Sauce, The Hungry Dragon brand, Net Wt. 22 oz (623 g), UPC 7-05105-61946-0 The label has the advisory statement: Produced in a facility that handles peanut, tree nuts, eggs, milk, wheat, and soy.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2807-2015·2015-07-15

    Boba Direct Pineapple Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling pineapple flavored powder due to undeclared allergens. The product was distributed in five states.

    Product
    Foil bags containing 2.2 lbs. each of pineapple flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2814-2015·2015-07-15

    Boba Direct Green Tea Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling green tea flavored powder due to undeclared allergens. The product was distributed in five US states.

    Product
    Foil bags containing 2.2 lbs. each of green tea flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2793-2015·2015-07-15

    Boba Direct banana flavored powder recalled for undeclared allergens

    Boba Direct, Inc. is recalling banana flavored powder in foil bags because the product contains undeclared allergens.

    Product
    Foil bags containing 2.2 lbs. each of banana flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2425-2015·2015-07-15

    New Punjab Ladoo Recalled for Missing Ingredient Label and Undeclared Allergens

    New Punjab Sweets Inc. is voluntarily recalling Ladoo snacks because they lack an ingredient label and may contain undeclared nuts, colors, and wheat.

    Product
    New Punjab Ladoo is a ball-shaped Indian snack coated with almonds and/or pistachios. Product is packaged in clear plastic container with a clear plastic lid. Container sizes are 1lb. and 0.5lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2797-2015·2015-07-15

    Boba Direct Chocolate Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling chocolate flavored powder for bubble tea due to undeclared allergens. The product was distributed in five states.

    Product
    Foil bags containing 2.2 lbs. each of chocolate flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2427-2015·2015-07-15

    New Punjab Rosgula Recalled for Undeclared Almonds, Colors, and Wheat

    New Punjab Sweets Inc. is voluntarily recalling Rosgula snacks due to undeclared almonds, colors, and wheat.

    Product
    New Punjab Rosgula is a ball-shaped Indian snack. Product is packaged in clear plastic container with a clear plastic lid. Container sizes are 1lb. and 0.5lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1990-2015·2015-07-15

    Maquet Surgical Light Suspension Arms Recalled for Debris Risk

    Maquet is recalling 646 PowerLED, X-TEN, and VOLISTA surgical light systems because suspension arms may grind and release paint chips into the surgical field.

    Product
    The PowerLED / X-TEN / VOLISTA Surgical Light Systems are surgical light systems intended to be used to provide visible illumination of the surgical area or the patient. Ceiling surgical light systems typically include one or more arms that are able to rotate 360 degrees around…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2791-2015·2015-07-15

    Boba Direct Almond Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling almond flavored powder due to undeclared allergens. The product was distributed in five states.

    Product
    Foil bags containing 2.2 lbs. each of almond flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1987-2015·2015-07-15

    Philips GoSafe Communicator 7000L Personal Emergency Response System Recall

    Lifeline Systems is recalling 38 Philips GoSafe Communicator 7000L units because they may fail to sense the phone line under unusual landline conditions.

    Product
    Philips GoSafe Communicator 7000L Personal emergency response system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2424-2015·2015-07-15

    New Punjab Kaju Fry Recalled for Undeclared Cashew Nuts

    New Punjab Sweets Inc. is voluntarily recalling Kaju Fry (toasted fried cashews) because the product may contain undeclared cashew nuts.

    Product
    New Punjab Kaju (Kajoo) Fry is the Indian translation for Toasted Fried Cashews. Product is packaged in clear plastic container with a clear plastic lid. Container sizes are 1lb. and 0.5lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2832-2015·2015-07-15

    D.A.M Brand Mild Salsa Recalled for Peanut Contamination

    Paradigm Foodworks is recalling D.A.M brand Mild Salsa due to potential peanut protein contamination. Consumers should check lot codes and stop using the product.

    Product
    Mild Salsa, D.A.M brand, Net Wt. 16 oz (453 g), UPC 1-87283-00001-6
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2828-2015·2015-07-15

    Masala Maza Korma Simmer Sauce Recalled for Peanut Contamination

    Paradigm Foodworks is recalling Masala Maza Korma Simmer Sauce due to potential peanut protein contamination. The product was distributed in four US states and Ontario, Canada.

    Product
    Korma Simmer Sauce, Masala Maza brand, Net Wt. 12 oz. (340 g), UPC 6-48253-10101-5. The label has the advisory statement: Made in a facility that uses peanut, tree nut, egg, milk, wheat, and soybeans.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2803-2015·2015-07-15

    Boba Direct Matcha Green Tea Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling matcha green tea flavored powder in 2.2 lb foil bags because the product contains undeclared allergens.

    Product
    Foil bags containing 2.2 lbs. each of matcha green tea flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighCPSC·15185·2015-07-15

    Bexco Recalls DaVinci Cribs Due to Entrapment and Fall Hazards

    Bexco is recalling DaVinci brand cribs because a metal bracket can break, creating gaps that pose entrapment, fall, and laceration risks to infants.

    Product
    DaVinci Cribs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2421-2015·2015-07-15

    New Punjab Burfi Recalled for Undeclared Nuts

    New Punjab Sweets Inc. is voluntarily recalling New Punjab Burfi because the Indian snack may contain undeclared almonds, pistachios, and cashews.

    Product
    New Punjab Burfi is an Indian snack cut into 1lb or 0.5 lb. squares. Product is packaged in clear plastic container with a clear plastic lid.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2426-2015·2015-07-15

    New Punjab Chum Chum Recalled for Undeclared Allergens and Colors

    New Punjab Sweets Inc. is voluntarily recalling Chum Chum snacks due to undeclared almonds, coconut, wheat, and food colors.

    Product
    New Punjab Chum Chum is a oval-shaped Indian snack coated with almonds and/or coconuts. Product is packaged in clear plastic container with a clear plastic lid. Container sizes are 1lb. and 0.5lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2838-2015·2015-07-15

    Ooga Booga N'Between BBQ Sauce Recalled for Peanut Contamination

    Paradigm Foodworks is recalling Ooga Booga N'Between BBQ Sauce due to potential peanut protein contamination. The product was distributed in four US states and Ontario, Canada.

    Product
    N'Between BBQ Sauce, Ooga Booga brand, Net wt. 17. 2 oz (498 g), UPC 8-13012-00437-5
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2802-2015·2015-07-15

    Boba Direct Mango Flavored Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling mango flavored powder in foil bags due to undeclared allergens. The product was distributed in Illinois, Missouri, Ohio, Florida, and Tennessee.

    Product
    Foil bags containing 2.2 lbs. each of mango flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2787-2015·2015-07-15

    Kerry Foods Recalls Non-Dairy Creamer Due to Potential Metal Fragments

    Kerry Foods is voluntarily recalling specific non-dairy creamer products produced in May 2015 due to the potential presence of small metal pieces from a broken production screen.

    Product
    Kraft Non-Dairy Creamer, Net WT/Contenido Neto 16 oz (454 g) SKU 2100042503. Kraft Non-Dairy Creamer, Net WT/Contenido Neto 6 oz (170g) SKU 2100042202. Country Barn, Coffee Creamer, Non-Dairy creamer, Net WT/Peso Neto 6 oz ( 170g), SKU 3540603606. Country Barn, Coffee…
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2799-2015·2015-07-15

    Boba Direct honeydew bubble tea powder recalled for undeclared allergens

    Boba Direct, Inc. is recalling honeydew flavored bubble tea powder because it contains undeclared allergens. The product was distributed in five US states.

    Product
    Foil bags containing 2.2 lbs. each of honeydew flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2808-2015·2015-07-15

    Boba Direct Red Bean Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling red bean flavored powder due to undeclared allergens. The product was distributed in Illinois, Missouri, Ohio, Florida, and Tennessee.

    Product
    Foil bags containing 2.2 lbs. each of red bean flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2798-2015·2015-07-15

    Boba Direct Coconut Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling coconut flavored powder due to undeclared allergens. The product was distributed in five US states.

    Product
    Foil bags containing 2.2 lbs. each of coconut flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2806-2015·2015-07-15

    Boba Direct Peppermint Bubble Tea Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling 2.2 lb foil bags of peppermint flavored bubble tea powder because they contain undeclared allergens. The product was distributed in Illinois, Missouri, Ohio, Florida, and Tennessee.

    Product
    Foil bags containing 2.2 lbs. each of peppermint flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1986-2015·2015-07-15

    BTE Technologies Recalls Primus Exercise Devices Due to Detachment Risk

    BTE Technologies is recalling 510 Primus rehabilitation devices because the optional Chop / Lift Bar may detach, posing a fall hazard to users.

    Product
    Primus (THE BTE WS30), model PrimusRS (PRRS) and Primus+ (PR30) a measuring exercise equipment device designed to provide active and passive torque resistance to patient motion during rehabilitation therapy. The Primus that includes the optional Chop / Lift Bar.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15186·2015-07-15

    Olympus Recalls VG 170 Digital Cameras Due to Electric Shock Hazard

    Olympus is recalling about 1,200 VG 170 digital cameras sold at HHGregg because an improperly installed part poses an electric shock risk. No injuries have been reported.

    Product
    Olympus VG 170 Digital Cameras
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2034-2015·2015-07-15

    Stradis Pediatric Pack Recalled Due to Medtronic Component Recall

    Stradis Healthcare is recalling Pediatric Packs containing Devon Light Gloves due to a manufacturer recall of the glove component by Medtronic.

    Product
    Pediatric Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2840-2015·2015-07-15

    Oregon Microbrew BBQ Sauce Recalled for Peanut Contamination

    Paradigm Foodworks is recalling Oregon Microbrew BBQ Sauce due to potential peanut protein contamination. The product was distributed in four US states and Ontario, Canada.

    Product
    Oregon Microbrew BBQ Sauce, Paradigm and Fess Parker brand, net wt. 12 fl. oz. (343 mL). The Paradigm has the UPC 0-37644-30520-8. The Fess Parker brand does not have UPC. The advisory statement on label is read "Made in a facility that handles peanuts, tree nuts, eggs…
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2804-2015·2015-07-15

    Boba Direct Milk Tea Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling milk tea flavored powder due to undeclared allergens. The product was distributed in five US states.

    Product
    Foil bags containing 2.2 lbs. each of milk tea flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2824-2015·2015-07-15

    Hungry Dragon BBQ Sauce Recalled for Potential Peanut Contamination

    Paradigm Foodworks is recalling Hungry Dragon Extra Spicy Stir Fry Marinade BBQ Sauce due to potential peanut protein contamination.

    Product
    Extra Spicy Stir Fry Marinade BBQ Sauce, the Hungry Dragon brand, Net Wt. 22 oz (623 g), UPC 7-01505-61996-5. The label has the advisory statement: Produced in a facility that handles peanut, tree nuts, eggs, milk, wheat, and soy.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2801-2015·2015-07-15

    Boba Direct Lychee Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling lychee flavored powder due to undeclared allergens. The product was distributed in five US states.

    Product
    Foil bags containing 2.2 lbs. each of lychee flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1993-2015·2015-07-15

    Stradis Basic Pack Recalled Due to Medtronic Component Recall

    Stradis Healthcare is recalling Basic Packs containing Devon Light Gloves because the manufacturer, Medtronic, is recalling the glove component.

    Product
    Basic Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2809-2015·2015-07-15

    Boba Direct Strawberry Bubble Tea Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling strawberry flavored bubble tea powder because it contains undeclared allergens. The product was distributed in five states.

    Product
    Foil bags containing 2.2 lbs. each of strawberry flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2805-2015·2015-07-15

    Boba Direct Passion Fruit Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling passion fruit flavored powder due to undeclared allergens. The product was distributed in five states.

    Product
    Foil bags containing 2.2 lbs. each of passion fruit flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2423-2015·2015-07-15

    New Punjab Kaju Roll Recalled for Undeclared Cashews and Colors

    New Punjab Sweets Inc. is voluntarily recalling Kaju Roll snacks because they may contain undeclared cashews and artificial colors Yellow 5 and 6.

    Product
    New Punjab Kaju Roll is an Indian snack cut into squares. Product is packaged in clear plastic container with a clear plastic lid. Container sizes are 1lb. and 0.5lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2839-2015·2015-07-15

    Ooga Booga Wild BBQ Sauce Recalled for Peanut Contamination

    Paradigm Foodworks is recalling Ooga Booga Wild BBQ Sauce due to potential peanut protein contamination. The product was distributed in four US states and Ontario, Canada.

    Product
    Wild BBQ Sauce, Ooga Booga brand, Net wt. 17. 6 oz (498 g), UPC 8-13012-00436-8
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2837-2015·2015-07-15

    Ooga Booga Mild BBQ Sauce Recalled for Peanut Contamination

    Paradigm Foodworks is recalling Ooga Booga Mild BBQ Sauce due to potential peanut protein contamination. The product was distributed in four US states and Ontario, Canada.

    Product
    Mild BBQ Sauce, Ooga Booga brand, Net wt. 17. 6 oz (498 g), UPC 8-13012-00435-1
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2041-2015·2015-07-15

    Stradis Arthroscopy Packs Recalled Due to Component Recall

    Stradis Healthcare is recalling Arthroscopy Packs because they contain Devon Light Gloves, which are being recalled by the manufacturer Medtronic.

    Product
    Arthroscopy Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2810-2015·2015-07-15

    Boba Direct Taro Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling taro flavored powder due to undeclared allergens. The product was distributed in five US states.

    Product
    Foil bags containing 2.2 lbs. each of taro flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2827-2015·2015-07-15

    D.A.M. Hot Salsa Recalled for Potential Peanut Contamination

    Paradigm Foodworks is recalling D.A.M. brand Hot Salsa due to potential contamination with peanut protein.

    Product
    Hot Salsa, D.A.M. brand, Net Wt. 16 oz (454 g), UPC 1-87283-00000-9
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2831-2015·2015-07-15

    D.A.M Brand Medium Salsa Recalled for Potential Peanut Contamination

    Paradigm Foodworks is recalling D.A.M brand Medium Salsa due to potential peanut protein contamination. The product was distributed in four US states and Ontario, Canada.

    Product
    Medium Salsa, D.A.M brand, Net Wt. 16 oz (453 g), UPC 1-87283-00002-3
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2834-2015·2015-07-15

    Hazelwood's Salsa Recalled for Potential Peanut Contamination

    Paradigm Foodworks is recalling Hazelwood's All Natural Mild Salsa due to potential contamination with peanut protein.

    Product
    Salsa, All Natural Mild, Hazelwood's brand, Net Wt. 16 oz (453 g), UPC 8-52707-00202-9
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2823-2015·2015-07-15

    Hazelwood's Cilantro Salsa Recalled for Potential Peanut Contamination

    Paradigm Foodworks is recalling Hazelwood's Cilantro Salsa due to potential peanut protein contamination. Consumers should check their pantry for the specific lot code.

    Product
    Cilantro Salsa, All Natural Medium, Hazelwood's brand, Net Wt. 16 oz. (454 g), UPC 8-52707-00206-7
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2826-2015·2015-07-15

    Hazelwood's Habanero Salsa Recalled for Potential Peanut Contamination

    Paradigm Foodworks is recalling Hazelwood's Habanero Salsa due to potential peanut contamination. The product was distributed in four US states and Ontario, Canada.

    Product
    Habanero Salsa, All Natural Hot, Hazelwood's brand, Net wt. 16 oz. (454 g), UPC 8-52707-00204-3
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2422-2015·2015-07-15

    New Punjab Kaju Katri Recalled for Undeclared Cashews and Colors

    New Punjab Sweets Inc. is voluntarily recalling Kaju Katri Indian snacks because they may contain undeclared cashews and artificial colors Yellow 5 and 6.

    Product
    New Punjab Kaju Katri is an Indian snack cut into squares. Product is packaged in clear plastic container with a clear plastic lid. Container sizes are 1lb. and 0.5lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2819-2015·2015-07-15

    Coalescence LLC Recalls Spicy Black Bean Burger Powder Mix for Undeclared Peanuts

    Coalescence LLC is recalling Spicy Black Bean Burger powder mix because it contains undeclared peanuts. The product was distributed to consignees in Ohio, Utah, and Michigan.

    Product
    Spicy Black Bean Burger powder mix, packaged in 30 LB poly-lined Kraft bags.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2829-2015·2015-07-15

    Soog Head Pineapple Smash Salsa Recalled for Peanut Contamination

    Paradigm Foodworks is recalling Soog Head Medium Pineapple Smash Salsa due to potential peanut protein contamination.

    Product
    Medium Pineapple Smash Salsa, Soog Head brand, Net Wt. 16 oz (453 g), UPC 6-26570-62023-5
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2813-2015·2015-07-15

    Boba Direct Spiced Chai Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling spiced chai flavored powder because it contains undeclared allergens. The product was distributed in five US states.

    Product
    Foil bags containing 2.2 lbs. each of spiced chai flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2821-2015·2015-07-15

    Rub with Love Barbecue Sauce Recalled for Peanut Contamination

    Paradigm Foodworks is recalling Rub with Love Ancho & Molasses Barbecue Sauce due to potential peanut protein contamination.

    Product
    Ancho & Molasses Barbecue Sauce, Rub with Love brand, Net wt. 16 oz., UPC 6-72361-00044-1
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2796-2015·2015-07-15

    Boba Direct Cherry Flavored Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling cherry flavored powder in foil bags due to undeclared allergens. The product was distributed in five states.

    Product
    Foil bags containing 2.2 lbs. each of cherry flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2830-2015·2015-07-15

    Soog Head Mild Pineapple Smash Salsa Recalled for Peanut Contamination

    Paradigm Foodworks is recalling Soog Head Mild Pineapple Smash Salsa due to potential contamination with peanut protein.

    Product
    Mild Pineapple Smash Salsa, Soog Head brand, Net Wt. 16 oz (453 g), UPC 6-26570-62024-2
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2792-2015·2015-07-15

    Boba Direct Recalls Avocado Flavored Powder for Undeclared Allergens

    Boba Direct, Inc. is recalling 2.2 lb foil bags of avocado flavored powder because they contain undeclared allergens. The product was distributed in five states.

    Product
    Foil bags containing 2.2 lbs. each of avocado flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighNHTSA·15V448000·2015-07-15

    Spartan Emergency Response Vehicles Recalled for Valve Stem Wear

    Spartan is recalling 2007-2015 emergency response vehicles because front wheel valve stems may rub against brake calipers, causing sudden tire deflation.

    Product
    SPARTAN — SPARTAN GLADIATOR, METROSTAR, ADVANTAGE, DIAMOND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2045-2015·2015-07-15

    Volcano ComboMap Intravascular System Recalled for Interoperability Limitation

    Volcano Corp is recalling 227 ComboMap Intravascular Flow and Pressure Systems due to a limitation in interoperability with the Philips Xper Flex Cardia Physiomonitoring System.

    Product
    ComboMap Intravascular Flow and Pressure System; Product/Part number: Combo Map - 802745-001. Intravascular Imaging and Pressure System for evaluation of blood flow, perfusion and vascular structures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2800-2015·2015-07-15

    Boba Direct Lavender Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling lavender flavored powder due to undeclared allergens. The product was distributed in five US states.

    Product
    Foil bags containing 2.2 lbs. each of lavender flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2795-2015·2015-07-15

    Boba Direct Cafe Latte Powder Recalled for Undeclared Allergens

    Boba Direct, Inc. is recalling cafe latte flavored powder for containing undeclared allergens. The product was distributed in five states.

    Product
    Foil bags containing 2.2 lbs. each of cafe latte flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2812-2015·2015-07-15

    Boba Direct Recalls Watermelon Powder for Undeclared Allergens

    Boba Direct, Inc. is recalling watermelon flavored powder due to undeclared allergens. The product was distributed in five US states.

    Product
    Foil bags containing 2.2 lbs. each of watermelon flavored powder and sold under the Boba Direct, Inc. brand.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-2023-2015·2015-07-15

    Stradis Healthcare Recalls Eye Packs Containing Recalled Devon Light Gloves

    Stradis Healthcare is recalling Eye Packs containing Devon Light Gloves due to a manufacturer recall of the glove component by Medtronic.

    Product
    Eye Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2789-2015·2015-07-15

    DASANI Purified Water Recalled for Potential Plastic Fragments

    World of Coca-Cola is recalling DASANI Purified Water because some bottles may contain linear pieces of plastic from the production process.

    Product
    DASANI Purified Water, 24/20 fl. oz. (1.25 pt) 591 mL, pack, Desani, The Coca Cola Company, Atlanta, GA 30313.
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-2021-2015·2015-07-15

    Stradis Gyn Pack Recalled Due to Medtronic Component Recall

    Stradis Healthcare is recalling Gyn Packs containing Devon Light Gloves because the manufacturer, Medtronic, recalled the glove component.

    Product
    Gyn Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2019-2015·2015-07-15

    Stradis Healthcare Recalls Abdominal Packs Containing Recalled Devon Light Gloves

    Stradis Healthcare is recalling Abdominal Packs and Abdom Packs because they contain Devon Light Gloves, a component recalled by Medtronic.

    Product
    Abdominal Pack and Abdom Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2012-2015·2015-07-15

    Stradis ACL Pack Recalled Due to Component Glove Recall

    Stradis Healthcare is recalling ACL Packs containing Devon Light Gloves because the manufacturer, Medtronic, is recalling the glove component.

    Product
    ACL Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2017-2015·2015-07-15

    Stradis Healthcare Recalls Bariatric Packs Containing Recalled Devon Light Gloves

    Stradis Healthcare is recalling Bariatric Packs because they contain Devon Light Gloves that are subject to a separate manufacturer recall by Medtronic.

    Product
    Bariatric Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1995-2015·2015-07-15

    Stradis Vein Surgery Packs Recalled Due to Component Issue

    Stradis Healthcare is recalling 55 vein surgery packs because they contain a Devon Light Glove component subject to a separate recall by Medtronic.

    Product
    Vein Pack, Vein Treatment II Pack, Vein Brunswick Pack, Vein No Lidocaine Pack, Vein Ablation Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1230-2015·2015-07-15

    Zonisamide capsules recalled for inadequate complaint investigation

    American Health Packaging is recalling Zonisamide capsules due to current good manufacturing practice deviations involving inadequate investigation of customer complaints.

    Product
    Zonisamide capsules, USP 100mg packaged in 10-count blisters (NDC 68084-008-11); 5 blister packs per carton (NDC 68084-008-65); Rx only, Manufactured by: Wockhardt Limited, Mumbai, India, Distributed by: Wockhardt, USA, LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA for…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2008-2015·2015-07-15

    Stradis Mississippi Pack Recalled Due to Medtronic Component Recall

    Stradis Healthcare is recalling Mississippi Packs containing Devon Light Gloves due to a manufacturer recall of the glove component.

    Product
    Mississippi Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2015-2015·2015-07-15

    Stradis Healthcare Recalls Skin and Vein Packs Containing Recalled Gloves

    Stradis Healthcare is recalling Skin and Vein Packs because they contain Devon Light Gloves that Medtronic is recalling.

    Product
    Skin and Vein Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2044-2015·2015-07-15

    Volcano Intravascular Ultrasound System Recalled for Interoperability Limitation

    Volcano Corp is recalling 227 Intravascular Ultrasound Imaging and Pressure Systems due to a limitation in interoperability with the Philips Xper Flex Cardia system that may impact Fraction Flow Reserve calculations.

    Product
    Volcano s5i/s5ix/s5iz/CORE Intravascular Ultrasound Imaging and Pressure System; Product/Part numbers: s5i -806300-020 ; s5ix/s5iz - 807400-001; CORE - 400-0 I 00.02. Intravascular Imaging and Pressure System for evaluation of blood flow, perfusion and vascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1226-2015·2015-07-15

    American Health Packaging Recalls Lisinopril Tablets Due to CGMP Deviations

    American Health Packaging is recalling 4,718 cartons of Lisinopril 5mg tablets due to inadequate investigation of customer complaints.

    Product
    Lisinopril tablets, USP 5mg packaged in 10-count blisters (NDC 68084-060-11); 10 blister packs per carton (NDC 68084-060-01); Rx only, Manufactured by: Wockhardt Limited, Mumbai, India, Distributed by: Wockhardt, USA, LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA for American…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2053-2015·2015-07-15

    RTI Surgical Recalls Songer Spinal Cable System Due to Labeling Error

    RTI Surgical is recalling 25 units of the Songer Spinal Cable System because the box end label incorrectly identifies the material as Titanium instead of Stainless Steel.

    Product
    Songer Spinal Cable System, Single Cable, Crimp, Bar, Stainless Steel, Sterile. The DePuy Spine Cable System can be utilized anywhere monofilament wire has been previously found to be indicated.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2043-2015·2015-07-15

    Volcano Intravascular Ultrasound System Recalled for Interoperability Limitation

    Volcano Corp is recalling 227 intravascular ultrasound systems due to a limitation that may affect Fraction Flow Reserve calculations when connected to specific Philips monitors.

    Product
    Volcano s5/s5x/CORE Mobile Intravascular Ultrasound Imaging and Pressure System; Product/Part numbers: s5 - 804200-002 and 804200-014; s5x - 807300-001; CORE MOBILE - 400-0100.01. Intravascular Imaging and Pressure System for evaluation of blood flow, perfusion and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2025-2015·2015-07-15

    Stradis Healthcare Recalls Shoulder Packs Containing Recalled Devon Light Gloves

    Stradis Healthcare is recalling surgical shoulder packs because they contain Devon Light Gloves that are subject to a separate manufacturer recall by Medtronic.

    Product
    Shoulder Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1225-2015·2015-07-15

    Famotidine tablets recalled for inadequate complaint investigation

    American Health Packaging is recalling 97,837 cartons of Famotidine tablets 20mg due to CGMP deviations involving inadequate investigation of customer complaints.

    Product
    Famotidine tablets, USP 20mg, packaged in 10-count blisters (NDC 68084-172-11); 10 blister packs per carton (NDC 68084-172-01); Rx only, Manufactured by: Wockhardt Limited, Mumbai, India, Distributed by: Wockhardt, USA, LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA for…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2007-2015·2015-07-15

    Stradis Surgical Packs Recalled Due to Medtronic Glove Component Issue

    Stradis Healthcare is recalling surgical and general surgery packs because they contain Devon Light Gloves, a component being recalled by Medtronic.

    Product
    Surgical Pack and General Surgery Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1217-2015·2015-07-15

    Mylan Recalls Capecitabine Tablets Due to Dissolution Failures

    Mylan Pharmaceuticals is recalling 1,068 bottles of Capecitabine Tablets, 500 mg, because the product failed to meet dissolution specifications.

    Product
    Capecitabine Tablets, USP, 500 mg, 120-count bottle, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505, NDC 0378-2512-78, UPC 3 0378-2512-78 6.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2009-2015·2015-07-15

    Stradis Face Lift Pack Recalled Due to Component Recall

    Stradis Healthcare is recalling Face Lift Packs because they contain a Devon Light Glove that is being recalled by its manufacturer, Medtronic.

    Product
    Face Lift Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1220-2015·2015-07-15

    Amlodipine besylate tablets recalled for inadequate complaint investigation

    American Health Packaging is recalling Amlodipine besylate tablets 10 mg due to current Good Manufacturing Practice (CGMP) deviations involving inadequate investigation of customer complaints.

    Product
    Amlodipine besylate tablets, USP 10 mg, packaged in 10-count blisters (NDC 68084-506-11); 10 blister packs per carton (NDC 68084-506-01); Rx only, Manufactured by: Wockhardt Limited, Mumbai, India, Distributed by: Wockhardt, USA, LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1233-2015·2015-07-15

    BioComp Pharma Recalls Subpotent Thera-Gesic Pain Relieving Creme Sachets

    BioComp Pharma is recalling 40,000 sachets of Thera-Gesic Pain Relieving Creme because the active ingredients menthol and methyl salicylate are below specification.

    Product
    Maximum Strength Analgesic Thera-Gesic Pain Relieving Creme Relief from: Joint and Muscle Soreness, Arthritis, Back Aches; 1/8 Oz Sachet, OTC, Manufactured for Mission Pharmacal Company 10999 IH 10 West, Suite 1000 San Antonio, TX 78230 by Mission Pharmacal Company 38505 IH 10…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1214-2015·2015-07-15

    Apotex Recalls Losartan Potassium Tablets for Uniformity Issues

    Apotex Inc. is recalling 23,076 bottles of Losartan potassium tablets 50 mg because the product may not meet blend uniformity specifications.

    Product
    Losartan potassium tablets USP, 50 mg, 90-count bottle, Rx only, Manufactured for Apotex Inc 150 Signet Drive, ON M9L1T9 by Apotex Research Private Limited, Plot 1 & 2, Bommasandra Industrial Area, 4th Phase Jigani Link Road, Bangalore, Karnataka, 560099, India NDC 60505-3161-9
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2006-2015·2015-07-15

    Stradis Tummy Tuck Pack Recalled Due to Component Defect

    Stradis Healthcare is recalling Tummy Tuck Packs because they contain a Devon Light Glove component that is subject to a separate recall by Medtronic.

    Product
    Tummy Tuck Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2051-2015·2015-07-15

    Synthes Recalls Three Titanium Tibial Nail End Caps for Missing Inspection

    Synthes is recalling three units of a titanium end cap for tibial nails because they were shipped before a required internal inspection was completed.

    Product
    TITANIUM END CAP WITH T40 STARDRIVE RECESS, 0MM EXTENSION FOR TITANIUM TIBIAL NAILS-EX; Synthes Tibial Nail System EX is intended to stabilize fractures of the proximal and distal tibia and the tibial shaft; open and closed tibial shaft fractures; certain pre-and post-isthmic…
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2001-2015·2015-07-15

    Stradis Vaginal Rejuvenation Pack Recalled Due to Component Recall

    Stradis Healthcare is recalling Vaginal Rejuvenation Packs because they contain a Devon Light Glove component that Medtronic is recalling.

    Product
    Vaginal Rejuvenation Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2037-2015·2015-07-15

    Stradis Blepharoplasty Packs Recalled Due to Component Recall

    Stradis Healthcare is recalling Blepharoplasty Packs because they contain Devon Light Gloves, which are subject to a separate recall by Medtronic.

    Product
    Blepharoplasty Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide

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