The Recall Desk

Archive

November 2017 recalls

629 recalls were announced in November 2017.

What the numbers show

Critical
72
Severe
168
High
284
Moderate
80
Low
25

Of the 629 recalls this month scored against our rubric, 11% are Critical, 27% are Severe.

Which agencies issued them

501–600 of 629

  • HighFDA (Food)·F-0108-2018·2017-11-08

    Potato Salad Recalled for Undeclared Egg Allergen

    ASK Foods is recalling Taste of Inspirations Classic Red Skin Potato Salad because it may contain undeclared egg.

    Product
    taste of Inspirations Classic Red Skin Potato Salad; Net Wt. 16 oz.,; Sell By: 10-20-2017 (top label). taste of Inspirations Rotini Salad; Ingredients: Rotini Pasta ect. Contains: Whey; Distributed by: DZA Brands, LLC, Salisbury, NC 28147/Scarborough, ME 04074; Keep Refrigerat
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0053-2018·2017-11-08

    Albertsons Recalls Ready Chef Go Trout Fillets for Listeria Risk

    Albertsons is recalling Ready. Chef. Go! Trout Fillets because they were produced with vegetable products recalled for potential Listeria monocytogenes.

    Product
    Ready. Chef. Go! Trout Fillet; UPC 234929 Items are made in store with generated scale label; sold as single, packaged items from refrigerated cases in the meat/seafood department or from mobile refrigerated merchandise cases. The scale label denotes the net weight of each pr
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0086-2018·2017-11-08

    Sid Wainer & Son Dried Chili Peppers Recalled for Undeclared Peanuts

    Sid Wainer & Son is recalling Jansal Valley brand Dried Chili De Arbol Peppers because the product contains undeclared peanuts.

    Product
    Sid Wainer & Son Jansal Valley brand Dried Chili De Arbol Peppers,packaged in a plastic clamshell container 1 ounce size
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0109-2018·2017-11-08

    Whole Foods Recalls Frosted Pumpkin Drop Cookies Due to Undeclared Walnuts

    Whole Foods Market is recalling approximately 1,300 units of Frosted Pumpkin Drop Cookies because walnuts are not listed in the ingredient statement.

    Product
    Frosted Pumpkin Drop Cookies; 2-oz.; sold in clear plastic clamshell container with PLU number 024767; UPC 24767000000
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0107-2018·2017-11-08

    Wegmans Dark Bulk Penny Choc Coins Recalled for Undeclared Soy

    Wegmans is recalling Dark Bulk Penny Choc Coins sold in the bakery due to undeclared soy lecithin.

    Product
    Wegmans Dark Bulk Penny Choc Coins, Sold in the Bakery Only UPC: 2-08016-00000
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0097-2018·2017-11-08

    Wegmans Brownies Recalled for Undeclared Peanuts

    Wegmans is recalling Original Killer Brownies with Pecans due to a supplier mix-up that may have introduced undeclared peanuts.

    Product
    Wegmans Original Killer Brownies with Pecans, UPC Number 2-08184-00000. The product is sold pre-packaged by the pound in a plastic clamshell, or individually on the self-serve cookie bar, in the Bakery Department at Wegmans stores.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0064-2018·2017-11-08

    Albertsons Recalls Steelhead Trout Fillets Due to Listeria Risk

    Albertsons is recalling Ready. Chef. Go! Steelhead Trout Fillets because they were produced with vegetable products recalled for potential Listeria monocytogenes.

    Product
    Ready. Chef. Go! Steelhead Trout Fillet UPC 234702 Items are made in store with generated scale label; sold as single, packaged items from refrigerated cases in the meat/seafood department or from mobile refrigerated merchandise cases. The scale label denotes the net weight
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0150-2018·2017-11-08

    Aunt Beths Cookies Recalled for Undeclared Peanut or Tree Nut Allergens

    Aunt Beths Cookies is voluntarily recalling multiple varieties of cookies sold between January 1, 2017, and September 28, 2017, due to potential undeclared peanut or tree nut allergens.

    Product
    Oatmeal Cookie, 60-2.5 oz. cookies, frozen
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·F-0055-2018·2017-11-08

    Albertsons Recalls Ready Chef Go Halibut Fillets for Listeria Risk

    Albertsons is recalling Ready. Chef. Go! Halibut Fillets because they were produced with vegetable products recalled for potential Listeria monocytogenes.

    Product
    Ready. Chef. Go! Halibut Fillet; UPC 231694 Items are made in store with generated scale label; sold as single, packaged items from refrigerated cases in the meat/seafood department or from mobile refrigerated merchandise cases. The scale label denotes the net weight of each
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0066-2018·2017-11-08

    Albertsons Recalls Ready Chef Go Catfish Fillets for Listeria Risk

    Albertsons is recalling Ready. Chef. Go! Catfish Fillets in Texas, Louisiana, and Arkansas because they were made with vegetable products recalled for potential Listeria monocytogenes.

    Product
    Ready. Chef. Go! Catfish Fillet UPC 239970 Items are made in store with generated scale label; sold as single, packaged items from refrigerated cases in the meat/seafood department or from mobile refrigerated merchandise cases. The scale label denotes the net weight of each p
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0145-2018·2017-11-08

    Aunt Beths Cookies Recalled for Undeclared Peanut and Tree Nut Allergens

    Aunt Beths Cookies is voluntarily recalling specific frozen cookie varieties sold between January 1, 2017, and September 28, 2017, due to potential undeclared peanut or tree nut allergens.

    Product
    Chocolate Chip-N-Chunk Cookie, 72- 2 oz. cookies, frozen
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·F-0148-2018·2017-11-08

    Aunt Beths Cookies Recalled for Undeclared Peanut and Tree Nut Allergens

    Aunt Beths Cookies is voluntarily recalling Red Velvet Cookies sold between January 1, 2017, and September 28, 2017, due to potential undeclared peanut or tree nut allergens.

    Product
    Red Velvet Cookie, 60- 2.5 oz. cookies, frozen
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·F-0057-2018·2017-11-08

    Albertsons Recalls Ready Chef Go Haddock Fillets Due to Listeria Risk

    Albertsons is recalling Ready. Chef. Go! Haddock Fillets in Texas, Louisiana, and Arkansas because they were made with vegetable products recalled for potential Listeria monocytogenes.

    Product
    Ready. Chef. Go! Haddock Fillet; UPC 231864 Items are made in store with generated scale label; sold as single, packaged items from refrigerated cases in the meat/seafood department or from mobile refrigerated merchandise cases. The scale label denotes the net weight of each
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0087-2018·2017-11-08

    Apple Valley Honey Roasted Crunch Recalled for Undeclared Almonds

    First Source, LLC is recalling Apple Valley Honey Roasted Crunch because the product contains undeclared almonds. The recall affects 32 cases distributed in six states.

    Product
    Apple Valley Honey Roasted Crunch, 15 lb. poly bag lined brown cardboard cases for bulk Item number: 5537606 UPC: 0 23637 02018 0
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0060-2018·2017-11-08

    Smiths Medical Recalls CADD Medication Cassette Reservoirs with Incorrect Pressure Plates

    Smiths Medical is recalling CADD Medication Cassette Reservoirs because some units may have been manufactured with an incorrect pressure plate.

    Product
    CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Nonvented stopper included., 50 mL, For use with CADD(R) pumps (except CADD-Micro(TM), CADD-MS(R) 3 and CADD-TPN(R) pumps)., REF 21-7001-24, STERILE EO, Smiths Medical ASD, Inc. For use with CADD(R) pumps (except
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0061-2018·2017-11-08

    Albertsons Recalls Ready Chef Go Shrimp for Potential Listeria

    Albertsons is recalling Ready. Chef. Go! Shrimp products in Texas, Louisiana, and Arkansas because they were made with vegetable products recalled for potential Listeria monocytogenes.

    Product
    Ready. Chef. Go! Shrimp 16/20 count UPC 234361; 26/30 count UPC 234362; 41/50 count UPC 234363 Items are made in store with generated scale label; sold as single, packaged items from refrigerated cases in the meat/seafood department or from mobile refrigerated merchandise
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0104-2018·2017-11-08

    Wegmans Cheese Filled Cannoli Recalled for Undeclared Soy Lecithin

    Wegmans is recalling Large Cheese Filled Cannoli products because they contain undeclared soy lecithin. Consumers in six states should stop eating the product.

    Product
    Wegmans Large Cheese Filled Cannoli, 2 Pack, 5 oz UPC: 0-77890-37951 Wegmans Large Cheese Cannoli, 4 Pack, 10 oz UPC: 0-77890-38014
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0062-2018·2017-11-08

    Smiths Medical Recalls CADD Medication Cassette Reservoirs with Incorrect Pressure Plate

    Smiths Medical ASD Inc. is recalling CADD Medication Cassette Reservoirs because some units may have been manufactured with an incorrect pressure plate.

    Product
    CADD(TM) Yellow Medication Cassette Reservoir with clamp and female Luer. Nonvented stopper included., REF 21-7100-24, 100mL, For use with CADD(R) pumps (except CADD-Micro(TM), CADD-MS(R) 3 and CADD-TPN(R) pumps).STERILE EO, Smiths Medical ASD, Inc. For use with CADD(R) pumps (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0054-2018·2017-11-08

    Biosense Webster Recalls THERMOCOOL Catheters Due to System Alert Error

    Biosense Webster is recalling THERMOCOOL catheters because they may trigger a false magnetic distortion alert on the CARTO 3 System, potentially leading to unintended ablation.

    Product
    THERMOCOOL SMARTTOUCH SF Uni-Directional Product Codes D-1347-01-S, D-1347-02-S, D-1347-03-S
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0138-2018·2017-11-08

    H-E-B Asian Noodle Cup Chicken Recalled for Listeria Risk

    H-E-B is recalling Asian Noodle Cup Chicken products because an ingredient may be contaminated with Listeria monocytogenes.

    Product
    H-E-B Asian Noodle Cup Chicken 24 oz. packaged in a plastic cup with a plastic insert and plastic lid.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0058-2018·2017-11-08

    Albertsons Recalls Ready Chef Go Mahi Mahi Fillets Due to Listeria Risk

    Albertsons is recalling Ready. Chef. Go! Mahi Mahi Fillets because they were produced with vegetable products recalled for potential Listeria monocytogenes.

    Product
    Ready. Chef. Go! Mahi Mahi Fillet; UPC 232426 Items are made in store with generated scale label; sold as single, packaged items from refrigerated cases in the meat/seafood department or from mobile refrigerated merchandise cases. The scale label denotes the net weight of eac
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0055-2018·2017-11-08

    Biosense Webster Recalls THERMOCOOL Catheters Due to Magnetic Distortion Alert

    Biosense Webster is recalling THERMOCOOL catheters because they may trigger a false magnetic distortion alert on the CARTO 3 System, potentially leading to unintended ablation.

    Product
    THERMOCOOL SMARTTOUCH SF Bi-Directional Product Codes D-1348-01-S, D-1348-04-S, D-1348-05-S
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0062-2018·2017-11-08

    Albertsons Recalls Ready Chef Go Gulf Shrimp for Potential Listeria

    Albertsons is recalling Ready. Chef. Go! Gulf Shrimp because they were made with vegetable products recalled for potential Listeria monocytogenes.

    Product
    Ready. Chef. Go! 21/25 count Gulf Shrimp UPC 234364 Items are made in store with generated scale label; sold as single, packaged items from refrigerated cases in the meat/seafood department or from mobile refrigerated merchandise cases. The scale label denotes the net weight
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0146-2018·2017-11-08

    Aunt Beths Cookies Recalled for Undeclared Peanut or Tree Nut Allergens

    Aunt Beths Cookies is voluntarily recalling specific frozen M&M Cookie products sold between January 1, 2017, and September 28, 2017, due to potential undeclared peanut or tree nut allergens.

    Product
    M&M Cookie, 60- 2.5 oz. cookies, frozen
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-0052-2018·2017-11-08

    Bios THERMI250 Radiofrequency System Recalled for Unintended Energy Emission

    Bios S.r.l. is recalling 167 THERMI250 Radiofrequency Systems because they may continue to emit RF energy after the PAUSE button is pressed.

    Product
    THERMI250 Radiofrequency System. Intended to provide heating for the purpose of elevating tissue temperature for selected medical conditions.
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Food)·F-0065-2018·2017-11-08

    Albertsons Recalls Ready Chef Go Seafood Meal Bags for Listeria Risk

    Albertsons is recalling Ready. Chef. Go! Kingclip Fillet meal bags in Texas, Louisiana, and Arkansas because they were made with vegetable products recalled for potential Listeria monocytogenes.

    Product
    Ready. Chef. Go! Kingclip Fillet UPC 239670 Items are made in store with generated scale label; sold as single, packaged items from refrigerated cases in the meat/seafood department or from mobile refrigerated merchandise cases. The scale label denotes the net weight of each
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0050-2018·2017-11-08

    Albertsons Recalls Ready. Chef. Go! Flounder Fillets for Potential Listeria

    Albertsons Inc is recalling Ready. Chef. Go! Flounder Fillets because they were produced with vegetable products recalled for potential Listeria monocytogenes.

    Product
    Ready. Chef. Go! Flounder Fillet; UPC 231495 Items are made in store with generated scale label; sold as single, packaged items from refrigerated cases in the meat/seafood department or from mobile refrigerated merchandise cases. The scale label denotes the net weight of each
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0151-2018·2017-11-08

    Aunt Beths Cookies Recalled for Undeclared Peanut and Tree Nut Allergens

    Aunt Beths Cookies is voluntarily recalling multiple varieties of cookies sold between January 1, 2017, and September 28, 2017, due to potential undeclared peanut or tree-nut allergens.

    Product
    Snickerdoodle Cookie, 60-2.5 oz. cookies, frozen
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·F-0106-2018·2017-11-08

    Wegmans Single Cheese Cannoli Recalled for Undeclared Soy Lecithin

    Wegmans is recalling Single Cheese Cannoli because they contain undeclared soy lecithin. Consumers should check their pantries and discard or return the product.

    Product
    Wegmans Single Cheese Cannoli, 2 oz. UPC: 0-77890-17163
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Drugs)·D-0069-2018·2017-11-08

    Teva Recalls Dutasteride and Tamsulosin HCl Capsules for Dissolution Failures

    Teva Pharmaceuticals is recalling specific lots of Dutasteride and Tamsulosin HCl capsules because they failed dissolution specifications.

    Product
    Dutasteride and Tamsulosin HCl Capsules, 0.5 mg/ 0.4 mg, packaged in a) 30-count bottle (NDC 0591-3771-30), b) 90-count bottle (NDC 0591-3771-19), Rx only, Manufactured by: Actavis Laboratories FL, Inc. Fort Lauderdale, FL 33314 USA; Distributed by: Actavis Pharma, Inc. Parsippan
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0057-2018·2017-11-08

    Precision Dose Recalls Subpotent Carbamazepine Oral Suspension Unit Dose Cups

    Precision Dose Inc. is recalling Carbamazepine Oral Suspension USP unit dose cups because they tested below the required potency specifications.

    Product
    Carbamazepine Oral Suspension USP, 100 mg/5 mL, 5 mL Unit Dose Cups (NDC 68094-301-59), packaged in 10-count cups per tray, 3 trays per case containing a total of 5 mL x 30 Unit Dose Cups per case (NDC 68094-301-62), Rx only, Pkg: Precision Dose, Inc., S. Beloit, IL 61080.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0055-2018·2017-11-08

    AvKARE Recalls Duloxetine Capsules Due to Slightly Elevated Phthalic Acid

    AvKARE is recalling 274 cartons of Duloxetine Delayed-release Capsules 20 mg due to slightly elevated levels of phthalic acid.

    Product
    Duloxetine Delayed-release Capsules USP, 20 mg, 50 Capsules (5 x 10) Unit Dose per carton, unit dose blister UPC 5026828311), Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-283-15.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0081-2018·2017-11-08

    Wegmans Turnovers Recalled for Undeclared Ingredients and Additives

    Wegmans is recalling assorted turnovers due to undeclared Yellow 5, Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.

    Product
    085194 - Wegmans Turnovers, Assorted, 2 Pack, 9 oz. UPC: 0 77890 85194 4
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-0084-2018·2017-11-08

    Wegmans Recalls Lemon Tart Filling for Undeclared Ingredients

    Wegmans is recalling 65 cases of Perfect Natural Lemon Tart Filling because the product contains undeclared FD&C Yellow 5, Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.

    Product
    549815- Fruit Fillings Inc. PERFECT NATURAL LEMON TART FILLING Net Weight 24 lb (10.88 kg) 12-2 lb tubes
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0061-2018·2017-11-08

    Smiths Medical Recalls CADD Medication Cassette Reservoirs with Incorrect Pressure Plate

    Smiths Medical is recalling CADD Medication Cassette Reservoirs that may have been manufactured with an incorrect pressure plate. The recall covers units distributed worldwide.

    Product
    CADD(TM) Medication Cassette Reservoir with clamp and female Luer., Nonvented stopper included., 100 mL, For use with CADD(R) pumps (except CADD-Micro(TM), CADD-MS(R) 3 and CADD-TPN(R) pumps).REF 21-7002-24, STERILE EO, Smiths Medical ASD, Inc. For use with CADD(R) pumps (excep
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0080-2018·2017-11-08

    Wegmans Half Cheese Danish Twist Recalled for Undeclared Ingredients

    Wegmans is recalling Half Cheese Danish Twists because they contain undeclared FD&C Yellow 5, Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.

    Product
    038973 - Wegmans Half Cheese Danish Twist, 6 oz. UPC: 0 77890 38973 7
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-0079-2018·2017-11-08

    Wegmans Cheese Danish Twist Recalled for Undeclared Ingredients

    Wegmans is recalling Cheese Danish Twist products containing undeclared Yellow 5, Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.

    Product
    038267 - Wegmans Cheese Danish Twist, 13 oz. UPC: 0 77890 38267 7
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-0083-2018·2017-11-08

    Wegmans Round Danish Recalled for Undeclared Ingredients

    Wegmans is recalling Round Danish products due to undeclared ingredients including FD&C Yellow 5 and Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.

    Product
    034208 Wegmans Round Danish, 6 pack. UPC: 0 77890 34208 4.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-0082-2018·2017-11-08

    Wegmans Puff Fruit Dumplings Recalled for Undeclared Ingredients

    Wegmans is recalling Puff Fruit Dumplings because they contain undeclared FD&C Yellow 5, FD&C Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.

    Product
    033710 - Wegmans Puff Fruit Dumplings, 2 Pack, 6 oz. UPC: 0 77890 33710 3
    Category
    Food
    Distribution
    5 states
  • LowFDA (Drugs)·D-0056-2018·2017-11-08

    Sanofi Recalls Clofarabine Injection Vials Due to Incorrect Package Insert

    Sanofi-Aventis is recalling 422 vials of Clofarabine injection because the authorized generic product was packaged with the incorrect package insert for the brand name product.

    Product
    Clofarabine injection, 20 mg/20 mL, 20 mL Single-Use Vial, Rx only, Mfd by: Teva Pharmachemle, Swensweg 5, Haarlem, The Netherlands; Mfd for: Winthrop U.S., a business of sanofi-aventis U.S. LLC, Bridgewater, NJ 08807; NDC 0955-1746-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·18025·2017-11-07

    Norco Recalls Children's Bicycles Due to Crank Failure Hazard

    Norco Bicycles is recalling specific children's models because the cranksets can bend or break during use, posing a fall hazard.

    Product
    Children's bicycles with Samox cranksets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V702000·2017-11-06

    Crysteel Recalls 2017 Dump Bodies for Driveshaft Detachment Risk

    Crysteel is recalling 2017 dump bodies built on Isuzu NRR-Series chassis because the driveshafts may detach from the rear universal joint, potentially causing loss of propulsion and increasing crash risk.

    Product
    CRYSTEEL — CRYSTEEL DUMP BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V699000·2017-11-06

    Forest River Recalls 2018 Puma Trailers for Incorrect Tire Placards

    Forest River is recalling 2018 Puma recreational trailers because the federal placards list incorrect tire size and pressure information, which could lead to over-inflation and tire failure.

    Product
    FOREST RIVER — FOREST RIVER PUMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V700000·2017-11-06

    Triumph Recalls 2016-2017 Speed Triple Motorcycles for Electrical Wiring Defect

    Triumph is recalling 2016-2017 Speed Triple S and R motorcycles because a charging system wire may rub against a bracket, potentially causing an electrical short and engine stall.

    Product
    TRIUMPH — TRIUMPH SPEED TRIPLE S, SPEED TRIPLE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V696000·2017-11-03

    Jayco Recalls 2016-2018 Jay Flight SLX Trailers Due to Fire Risk

    Jayco is recalling 2016-2018 Jay Flight SLX trailers because the battery circuit lacks overcurrent protection, increasing fire risk during electrical shorts.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT SLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V697000·2017-11-03

    Highland Ridge Recalls 2018 Light Trailers Due to Underrated Safety Chains

    Highland Ridge RV is recalling 2018 Light recreational trailers because the safety chains are rated for a lower weight than the trailer's actual capacity, increasing crash risk if detached.

    Product
    HIGHLAND RIDGE FW — HIGHLAND RIDGE FW LIGHT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V695000·2017-11-03

    Entegra Motorhomes Recalled for Missing Exterior Reflectors

    Entegra is recalling 2016-2018 Aspire, Anthem, Cornerstone, and Insignia motorhomes because they lack required reflectors, reducing visibility to other drivers.

    Product
    ENTEGRA — ENTEGRA ANTHEM, ASPIRE, INSIGNIA, CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·18022·2017-11-02

    Kidde Recalls Fire Extinguishers with Plastic Handles Due to Failure to Discharge

    Kidde is recalling fire extinguishers with plastic handles and Pindicator models because they may fail to discharge or have nozzles detach. One death and 16 injuries have been reported.

    Product
    Kidde fire extinguishers with plastic handles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V694000·2017-11-02

    Van-Con Recalls Dual Rear Wheel School Buses Due to Seat Barrier Defect

    Van-Con is recalling 2007-2017 Dual Rear Wheel school buses because the seat barrier behind the driver may be pinned, preventing it from deforming in a crash.

    Product
    VAN-CON — VAN-CON DUAL REAR WHEEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·117-2017·2017-11-02

    CC Kitchens Recalls Meat and Poultry Products Produced Without Inspection

    CC Kitchens LLC is recalling approximately 269 pounds of ready-to-eat meat and poultry products produced without federal inspection in Ohio.

    Product
    CC Kitchens LLC Recalls Meat and Poultry Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·17V692000·2017-11-02

    Thor Motor Coach Recalls 2018 Motorhomes Due to Trailer Light Wiring Defect

    Thor Motor Coach is recalling 2018 Ace, Axis, Hurricane, Windsport, and Vegas motorhomes because trailer light wiring may be inserted incorrectly, causing lights to fail and increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH ACE, AXIS, WINDSPORT, HURRICANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0038-2018·2017-11-01

    Myanmar Wholesale Trading Recalls Thanlwin Fried Bean Snack for Undeclared Peanuts

    Myanmar Wholesale Trading is recalling Thanlwin Fried Bean Snack due to undeclared peanuts. The product was distributed in Iowa, Illinois, Indiana, and Minnesota.

    Product
    Thanlwin Fried Bean Snack, Net Weight 227 g 8 oz.. UPC 84682-00095 Product of Myanmar.
    Category
    Food
    Distribution
    4 states
  • CriticalUSDA FSIS·116-2017·2017-11-01

    Chelsea Food Services Recalls Pork and Chicken Burritos for Listeria

    Chelsea Food Services is recalling approximately 28,064 pounds of frozen pork and chicken burritos and wraps due to possible Listeria monocytogenes contamination.

    Product
    Chelsea Food Services Firm Recalls Pork and Chicken Products Due To Possible Listeria Contamination
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Drugs)·D-0031-2018·2017-11-01

    Lucky Mart Recalls Piyamping Anti-Itch Lotion Due to Incorrect Formulation

    Lucky Mart Inc. is recalling Piyamping Anti-Itch Lotion because it contains dexamethasone instead of the labeled hydrocortisone.

    Product
    PIYANPING Anti-Itch (hydrocortisone) Lotion, 1%, Net Wt. 0.67 oz (20g) tube, Manufactured By: Jimin Pharmaceutial Co., LTD., Distributor: Lucky Mart, El Monte, CA 91733, NDC 68085-8012-4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0032-2018·2017-11-01

    Vitility Recalls MAN OF STEEL Capsules Containing Undeclared Sildenafil

    Vitility is recalling MAN OF STEEL capsules because FDA analysis found they contain undeclared sildenafil, an unapproved drug with unestablished safety and efficacy.

    Product
    MAN OF STEEL capsules, 3000mgs/grain, 1-count packets, Packaged for: One Drop Solutions, LLC, POB 231693, Sacramento, California 95823; [email protected]; www.manofsteelpills.com; UPC 1 0001001378 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0036-2018·2017-11-01

    365 Organic Raisin Bran Flakes Recalled for Undeclared Peanut Allergen

    Whole Foods Market Brand 365 is recalling 365 Organic Raisin Bran Flakes because peanut butter and cocoa balls were mistakenly packaged in the boxes, creating an undeclared peanut allergen risk.

    Product
    365 Organic Raisin Bran Flakes 15 oz. packaged in plastic bag, then cardboard box
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0023-2018·2017-11-01

    Banner Pharmacy Recalls Oxytocin Infusion Bags Due to Sterility Concerns

    Banner Pharmacy Services is recalling Oxytocin 30 units in 0.9% Sodium Chloride bags because the FDA determined there is a lack of assurance of sterility.

    Product
    OXYtocin 30 units added to 0.9% Sodium Chloride 500 mL bag, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 95226, NDC 7025000101
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0021-2018·2017-11-01

    OriGen Reinforced Dual Lumen Catheter Recalled for Tube Separation

    OriGen Biomedical is recalling 180 units of Reinforced Dual Lumen Catheters because the extension tube may separate from the hub, causing patient injury.

    Product
    The OriGen Reinforced Dual Lumen catheter (RDLC) is a duel lumen catheter with a wire reinforcement layer on the tip of the device. A thin sheath is used to cover and secure the wire layer and is heat shrunk into a permanent position.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0039-2018·2017-11-01

    Great American Deli Recalls Chicken Salad Sandwiches for Undeclared Allergens

    Great American Deli is recalling 816 chicken salad sandwiches because they contain undeclared eggs and soy. The product was distributed in Michigan, Kentucky, Tennessee, and Georgia.

    Product
    GREAT AMERICAN DELI PREMIUM CHICKEN SALAD WHEATBERRRY sandwiches are packaged in a flexible plastic containers, NET WT. 6.4 oz (181g), Great American Deli, PO Box 27, Ooltewah, TN 37363 UPC 7 41431 00228 6
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0018-2018·2017-11-01

    Banner Pharmacy Recalls Fentanyl Citrate Syringes Due to Sterility Concerns

    Banner Pharmacy Services is recalling fentanyl citrate syringes because the agency could not ensure the product was sterile.

    Product
    fentanyl citrate (PF) 1100 mcg (20 mcg/mL) 55 mL syringes in 0.9% Sodium Chloride, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 95226, NDC 7025011001
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0037-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Injection Bags Nationwide

    Pharmedium Services, LLC is voluntarily recalling 2,232 bags of compounded Oxytocin injection because the drug was found to be subpotent.

    Product
    Oxytocin 15 units added to 250 mL Lactated Ringer's Injection USP in 250 mL bag, Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130, Sugar Land, TX 77478, NDC# 71019-239-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0043-2018·2017-11-01

    MicroPort Orthopedics Recalls 48 Schanz Screws Due to Seal Defect

    MicroPort Orthopedics is recalling 48 sterile Schanz screws due to an inadequate pouch seal that could compromise sterility and lead to infection.

    Product
    MicroPort Orthopedics SCHANZ SCREW SELF DRILL, SIZE 4mm, REF 20070057, STERILE R Product Usage: MPO Total Hip Systems are indicated for use in total hip arthroplasty for reduction or relief of pain and/or improved hip function in skeletally mature patients with the following
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0048-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Infusion Bags Nationwide

    Pharmedium Services, LLC is voluntarily recalling 90 bags of compounded Oxytocin 40 units in Lactated Ringer's because the drug was subpotent.

    Product
    Oxytocin 40 units added to 1000 mL Lactated Ringer's USP in 1000 mL bag, Rx Only , Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130, Sugar Land, TX 77478, NDC# 71019-245-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0038-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Injection Bags Nationwide

    Pharmedium Services, LLC is voluntarily recalling Oxytocin 20 units in Lactated Ringer's Injection USP bags because the drug was found to be subpotent.

    Product
    Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection USP in 1000 mL bag, Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-241-06
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0020-2018·2017-11-01

    Banner Pharmacy Recalls Magnesium Sulfate IV Bags Due to Sterility Concerns

    Banner Pharmacy Services is recalling 7,578 bags of Magnesium sulfate 10 Gm in Lactated Ringer's due to a lack of assurance of sterility.

    Product
    Magnesium sulfate 10 Gm added to Lactated Ringer's 250 mL bags, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 95226, NDC 7025003201
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0028-2018·2017-11-01

    Banner Pharmacy Recalls Norepinephrine Bags Due to Sterility Concerns

    Banner Pharmacy Services is recalling 481 bags of Norepinephrine Bitartrate in 0.9% Sodium Chloride due to a lack of assurance of sterility.

    Product
    Norepinephrine Bitartrate16 mg added to 0.9% Sodium Chloride 250 mL bag, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 85226, NDC 7025014801
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0043-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Infusion Bags Nationwide

    Pharmedium Services, LLC is voluntarily recalling 4,452 bags of compounded Oxytocin 30 units due to subpotent drug levels. The FDA classified this as a Class II recall.

    Product
    Oxytocin 30 units added to 500 mL 5% Dextrose/Lactated Ringer's USP in 500 mL bag, Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-242-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0027-2018·2017-11-01

    Banner Health Recalls Vancomycin Bags Due to Sterility Concerns

    Banner Pharmacy Services is recalling 2,443 bags of Vancomycin in sodium chloride due to a lack of assurance of sterility.

    Product
    VANCOmycin 1.25 grams added to 0.9% Sodium Chloride 500 mL bag, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 95226, NDC 7025007001
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0024-2018·2017-11-01

    Banner Pharmacy Recalls Ropivacaine HCL Cassettes Due to Sterility Concerns

    Banner Pharmacy Services is recalling Ropivacaine HCL cassettes because the FDA determined there is a lack of assurance of sterility.

    Product
    Ropivacaine HCL (PF) 0.2% (2mg/mL) 100 mL Cassette Rx Only Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 95226 NDC 7025006301
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0017-2018·2017-11-01

    Fentanyl Citrate Infusion Cassettes Recalled for Sterility Assurance Concerns

    Banner Pharmacy Services is recalling fentanyl citrate infusion cassettes due to a lack of assurance of sterility. The affected products were distributed nationwide.

    Product
    fentaNYL citrate 1000 mcg (10 mcg/mL) 100 mL Cassette in 0.9% Sodium Chloride, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 85226, NDC 7025011001
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0022-2018·2017-11-01

    Banner Pharmacy Recalls Norepinephrine Bags Due to Sterility Concerns

    Banner Pharmacy Services is recalling 3,550 bags of Norepinephrine Bitartrate 8 mg in 0.9% Sodium Chloride due to a lack of assurance of sterility.

    Product
    Norepinephrine Bitartrate 8 mg added to 0.9% Sodium Chloride 250 mL in a bag, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 95226, NDC 7025011501
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0036-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Injection Bags Nationwide

    Pharmedium Services, LLC is recalling 1,308 bags of compounded Oxytocin 10 units in Lactated Ringer's Injection because the drug was subpotent.

    Product
    Oxytocin 10 units added to 500 mL Lactated Ringer's Injection USP in 500 mL bag ,Rx Only , Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130, Sugar Land, TX 77478, NDC# 71019-237-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0019-2018·2017-11-01

    FDA Recalls Hydromorphone Syringes Due to Sterility Concerns

    Banner Pharmacy Services is recalling specific lots of Hydromorphone HCl syringes because the FDA determined there is a lack of assurance of sterility.

    Product
    Hydromorphone HCl 10 mg (0.2mg/ml) 50 mL syringes in 0.9% Sodium Chloride, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 95226, NDC 7025001001.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0045-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Infusion Bags Nationwide

    Pharmedium Services, LLC is voluntarily recalling 763 bags of compounded Oxytocin 30 units in Lactated Ringer's USP. The recall was initiated because the drug was found to be subpotent.

    Product
    Oxytocin 30 units added to 1000 mL Lactated Ringer's USP in 1000 mL bag Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-243-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0047-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Infusion Bags Nationwide

    Pharmedium Services, LLC is voluntarily recalling 24,486 bags of compounded Oxytocin 30 units in Lactated Ringer's because the drug was subpotent.

    Product
    Oxytocin 30 units added to 500 mL Lactated Ringer's USP in 500 mL bag, Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-243-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0042-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Infusion Bags Nationwide

    Pharmedium Services, LLC is voluntarily recalling 534 bags of compounded Oxytocin 30 units in 1000 mL bags because the drug was found to be subpotent.

    Product
    Oxytocin 30 units added to 1000 mL 5% Dextrose/Lactated Ringer's USP in 1000 mL bag, Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-242-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0044-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Infusion Bags Nationwide

    Pharmedium Services is recalling 6,108 bags of compounded Oxytocin 30 units in Lactated Ringer's because the drug was subpotent. The recall is voluntary and nationwide.

    Product
    Oxytocin 30 units added to 500 mL Lactated Ringer's USP in 500 mL bag Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130, Sugar Land, TX 77478, NDC# 71019-243-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0026-2018·2017-11-01

    Banner Pharmacy Recalls Vancomycin Bags Due to Sterility Concerns

    Banner Pharmacy Services is recalling 3,136 bags of Vancomycin 1.5 grams in 0.9% Sodium Chloride due to a lack of assurance of sterility.

    Product
    VANCOmycin 1.5 grams added to 0.9% Sodium Chloride 500 mL bag, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 95226, NDC 7025002501
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0021-2018·2017-11-01

    Banner Pharmacy Recalls Midazolam Cassettes Due to Sterility Concerns

    Banner Pharmacy Services is recalling 966 cassettes of Midazolam HCL 100 mg due to a lack of assurance of sterility. The affected products were distributed nationwide.

    Product
    Midazolam HCL 100 mg (1mg/mL) 100 mL Cassette in 0.9% Sodium Chloride, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 95226, NDC 7025016201
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0025-2018·2017-11-01

    Banner Pharmacy Recalls Succinylcholine Syringes Due to Sterility Concerns

    Banner Pharmacy Services is recalling 2,792 syringes of Succinylcholine 200 mg/10 mL because the product lacks assurance of sterility.

    Product
    Succinylcholine 200 mg/10 mL Syringe, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 95226, NDC 7025088801
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0049-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Infusion Bags Nationwide

    Pharmedium Services is voluntarily recalling 42 bags of compounded Oxytocin 40 units in Lactated Ringer's solution because the drug was subpotent.

    Product
    Oxytocin 40 units added to 1000 mL Lactated Ringer's USP in 1000 mL bag Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-245-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0041-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Injection Bags Nationwide

    Pharmedium Services, LLC is voluntarily recalling 60 bags of compounded Oxytocin injection because the drug was found to be subpotent.

    Product
    Oxytocin 20 units added to 500 mL Lactated Ringer's Injection USP in 500 mL bag Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-241-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0015-2018·2017-11-01

    Banner Pharmacy Recalls Diltiazem HCL Bags Due to Sterility Concerns

    Banner Pharmacy Services is recalling 1,359 bags of Diltiazem HCL 125 mg in 0.9% Sodium Chloride due to a lack of assurance of sterility.

    Product
    Diltiazem HCL 125 mg added to 0.9% Sodium Chloride 100 ml bag, 125 mL bag, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 85226, NDC 7025018601
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0035-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Injection Bags Nationwide

    Pharmedium Services, LLC is voluntarily recalling 564 bags of compounded Oxytocin 10 units in Lactated Ringer's Injection because the drug was subpotent.

    Product
    Oxytocin 10 units added to 1000 mL Lactated Ringer's Injection USP in 1000 mL bag, Rx Only , Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130, Sugar Land, TX 77478, NDC# 71019-237-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0035-2018·2017-11-01

    Weis Markets Recalls BLT Sandwiches Due to Undeclared Egg Allergen

    Weis Markets is recalling store-made BLT sandwiches because the mayonnaise contains undeclared egg. The recall follows a consumer complaint regarding the missing allergen label.

    Product
    Weis, Sunbury, PA; BLT Sandwich; 1 CT
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0016-2018·2017-11-01

    Banner Pharmacy Recalls Ephedrine Sulfate Syringes Due to Sterility Concerns

    Banner Pharmacy Services is recalling ephedrine sulfate syringes because the company cannot ensure the product is sterile.

    Product
    ePHEDrine sulfate 50 mg/10 ml syringes in 0.9% Sodium Chloride, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 85226, NDC 7025024801
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0037-2018·2017-11-01

    General Mills Recalls Cascadian Farm Granola for Undeclared Almond Allergen

    General Mills is recalling specific lots of Cascadian Farm Organic Cinnamon Raisin Granola because they contain undeclared almonds, a major food allergen.

    Product
    Cascadian Farm Organic Cinnamon Raisin Granola, Net Wt 15.6 oz (442g). UPC 21908-74329
    Category
    Food
    Distribution
    Distributed nationwide

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