The Recall Desk

Archive

March 2019 recalls

999 recalls were announced in March 2019.

What the numbers show

Critical
265
Severe
394
High
255
Moderate
69
Low
16

Of the 999 recalls this month scored against our rubric, 27% are Critical, 39% are Severe.

Which agencies issued them

601–700 of 999

  • SevereFDA (Drugs)·D-0541-2019·2019-03-20

    FDA Recalls King Bio Homeopathic Liver Detox Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Liver Detox due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's Natural Medicine Homeopathic Liver Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955006220, NDC 57955-5062-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0746-2019·2019-03-20

    King Bio Recalls Dr. King's SafeCare Rx Snore Control Sleep

    King Bio Inc. is recalling Dr. King's SafeCare Rx Snore Control Sleep due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Snore Control Sleep, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955012023, NDC 57955-0120-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0856-2019·2019-03-20

    King Bio Recalls ChemoClenz Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx ChemoClenz due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx ChemoClenz, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955007128, NDC 57955-0071-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0908-2019·2019-03-20

    King Bio Recalls Safecare+ AsthmaCare Homeopathic Due to Microbial Contamination

    King Bio Inc. is recalling Safecare+ AsthmaCare Homeopathic bottles due to microbial contamination. The product is distributed in the U.S., Canada, and Australia.

    Product
    Safecare+ AsthmaCare Homeopathic, Not a Rescue Inhaler, 1 fl oz (29.6 mL), UPC 357955704416, NDC 57955-7044-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0546-2019·2019-03-20

    King Bio Homeopathic Nuts & Seeds Intolerances Recalled for Microbial Contamination

    King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Nuts & Seeds Intolerances due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's Natural Medicine Homeopathic Nuts & Seeds Intolerances, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955520528, NDC 57955-5205-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0923-2019·2019-03-20

    King Bio Inc. Recalls NET Remedies #7 Homeopathic Preparation Due to Microbial Contamination

    King Bio Inc. is recalling NET Remedies #7 Homeopathic Preparation, Oral Liquid, 57 mL, due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    NET Remedies #7 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0543-2019·2019-03-20

    FDA Recalls Homeopathic Restless Leg Symptom Relief Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Restless Leg Symptom Relief due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's Natural Medicine Homeopathic Restless Leg Symptom Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955544524, NDC 57955-6235-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0712-2019·2019-03-20

    King Bio Recalls Colds and Flu Immune Syrup Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Colds & Flu Immune syrup due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Colds & Flu Immune, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955038221, NDC 57955-0382-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0724-2019·2019-03-20

    King Bio Recalls Indecision Mind & Body Due to Microbial Contamination

    King Bio Inc. is recalling 22 bottles of Dr. King's SafeCare Rx Indecision Mind & Body due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Indecision Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955277026, NDC 57955-2771-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0809-2019·2019-03-20

    King Bio Recalls Cough Control Syrup Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Cough Control due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Cough Control, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955016625, NDC 57955-0166-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0577-2019·2019-03-20

    King Bio Homeopathic Blood & Kidney Detox Recalled for Microbial Contamination

    King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Blood & Kidney Detox due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's Natural Medicine Homeopathic Blood & Kidney Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955506126, NDC 57955-5061-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0771-2019·2019-03-20

    FDA Recalls Dr. King's SafeCare Rx PMS Relief Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx PMS Relief bottles due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx PMS Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955000921, NDC 57955-0095-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0651-2019·2019-03-20

    King Bio Recalls Homeopathic Cold & Damp Product Due to Microbial Contamination

    King Bio Inc. is recalling 15 bottles of Dr. King's Natural Medicine Homeopathic Climate Adaptation Cold & Damp due to microbial contamination.

    Product
    Dr. King's Natural Medicine Homeopathic Climate Adaptation Cold & Damp, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955528425, NDC 57955-0170-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1006-2019·2019-03-20

    FDA Recalls NexGen Trabecular Metal Tibial Augments Due to Labeling Mismatch

    Zimmer Trabecular Metal Technology is recalling 26 units of NexGen Trabecular Metal Tibial Half Block Augments because the product in the box may not match the label.

    Product
    NexGenTrabecular Metal Tibial Half Block Augment, Left Lateral/Right Medial, Size 4 5MM Thickness W/Screws Item Number: 00544800436 Product Usage: The Trabecular Metal Tibial Cone Augments are intended for use where severe degeneration, trauma, or other pathology of the kne
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0583-2019·2019-03-20

    Dr. King's Natural Medicine Homeopathic Foul Bowel is recalled due to microbial contamination.

    An FDA drug recall affects Dr. King's Natural Medicine Homeopathic Foul Bowel because microbial contamination was detected. Consumers should stop using the product immediately.

    Product
    Dr. King's Natural Medicine Homeopathic Foul Bowel, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955531920, NDC 57955-5319-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·19088·2019-03-20

    Honda Recalls Portable Generators Due to Fire and Burn Hazards

    American Honda is recalling approximately 200,000 portable generators because a fuel valve leak can cause fire and burn hazards. No injuries have been reported.

    Product
    Honda EU2200i, EU220i Companion and EB2200i Portable Generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1222-2019·2019-03-20

    Joy Green Chilli Chutney Recalled for Undeclared Sulfites

    Joy Gourmet Foods LLC is recalling Joy Green Chilli Chutney because it contains undeclared sulfites. The product was distributed in Connecticut, New York, and New Jersey.

    Product
    JOY GREEN CHILLI CHUTNEY NET WT 8 OZ (228g), UPC: 6 80617 60412 1
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1011-2019·2019-03-20

    US Endoscopy Padlock Clip Recalled for Potential Esophageal Laceration Risk

    US Endoscopy Group Inc is recalling Padlock Clip defect closure systems due to a risk of esophageal laceration during patient procedures.

    Product
    US Endoscopy Padlock Clip defect closure system Ref: C910001 The Padlock Clip is indicated for use in flexible endoscopy and for the compression of tissue in the gastrointestinal tract, for hemostasis or for treating lesions of the wall of the gastrointestinal organs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1002-2019·2019-03-20

    Roberts Home Medical Recalls Refrigerated Liquid Oxygen Cylinders Due to CGMP Deviations

    Roberts Home Medical LLC is voluntarily recalling 9 refrigerated liquid oxygen reservoirs due to Current Good Manufacturing Practice (CGMP) deviations. The product was distributed in Maryland, Virginia, and the District of Columbia.

    Product
    Oxygen, Refrigerated Liquid USP, Rx only, cylinder, a) Roberts Home Medical, Inc. Rockville MD 20855, b) Roberts Home Medical, Inc. Germantown, MD. 20875
    Category
    Drug
    Distribution
    3 states
  • HighNHTSA·19V218000·2019-03-20

    Volkswagen Atlas and Passat Recall for Incorrect Side Air Bags

    Volkswagen is recalling 2019 Atlas and 2020 Passat vehicles because incorrect side air bags may have been installed, potentially failing to deploy in a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, PASSAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1155-2019·2019-03-20

    Perrigo Recalls Simple Truth Organic Fruit Puree Pouches for Milk Labeling Error

    Perrigo is voluntarily recalling Simple Truth Organic Fruit Puree pouches because the packaging fails to declare the presence of milk.

    Product
    Simple Truth Organic Banana, Strawberry & Apple Fruit Puree with Nonfat Greek Yogurt, 113 g, packed in a laminate pouch, Each case has 6 cartons with 6 pouches per carton. Total of 36 pouches per case.
    Category
    Food
    Distribution
    16 states
  • HighFDA (Devices)·Z-0994-2019·2019-03-20

    Durex Pleasure Pack Condoms Recalled for Burst Pressure Failure

    Reckitt Benckiser is recalling Durex Pleasure Pack condoms because five batches failed burst pressure specifications.

    Product
    Durex Pleasure Pack (60 ct), synthetic polisoprene male condom, SKU 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1212-2019·2019-03-20

    Joy Natural Tamarind Concentrate Recalled for Undeclared Sulfites

    Joy Gourmet Foods LLC is recalling Joy Natural Tamarind Concentrate because the product contains undeclared sulfites. The recall affects 14 oz and 32 oz bottles distributed in Connecticut, New York, and New Jersey.

    Product
    JOY NATURAL TAMARIND CONCENTRATE Net Wt.: 14FL OZ. (400g), UPC: 6 80617 60020 8 and Net Wt.: 32 FL Oz. (915g) UPC: 6 80617 60021 5
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1184-2019·2019-03-20

    Victoria Marinara Sauce Recalled for Undeclared Cashews

    B&G Foods is recalling Victoria Marinara Sauce because it may contain undeclared cashews, a major food allergen.

    Product
    Victoria Marinara Sauce, 40 oz. (2.5 lb) 1133g, 6Jars / Case
    Category
    Food
    Distribution
    4 states
  • HighNHTSA·19V221000·2019-03-20

    Osage Ambulances Recalled for Brake Lights Illuminating Without Pedal Press

    Osage is recalling 2015-2019 Brave, Warrior, and Super Warrior ambulances because brake lights may illuminate when the brake pedal is not pressed, potentially confusing other drivers.

    Product
    OSAGE — OSAGE BRAVE, WARRIOR, SUPER WARRIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1159-2019·2019-03-20

    Albertsons Signature Cafe Tomato Basil Bisque Soup Recalled for Foreign Object

    Albertsons is recalling 500 cases of Signature Cafe Tomato Basil Bisque Soup because a temperature data logger may be inside a retail package.

    Product
    Signature Caf¿ Tomato Basil Bisque Soup: polypropylene cups with linear low density polyethylene caps, and with plastic film seal. NET WT: 24 oz. (1 lb.. 8 oz.) 680 g Perishable, Keep Refrigerated. UPC 0002113015645 Distributed by: Lucerne Foods, Inc., P. P. Box 99, Pleasa
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1216-2019·2019-03-20

    JOY Tamarind and Dates Chutney Recalled for Undeclared Sulfites

    JOY Gourmet Foods LLC is recalling Tamarind and Dates Chutney because it contains undeclared sulfites. The product was distributed in Connecticut, New York, and New Jersey.

    Product
    JOY Tamarind and Dates Chutney (SWEET N' SOUR SAUCE), NET WT 8 OZ (228g), UPC: 6 80617 60437 4 and NET WT: 16 OZ (456g), UPC: 6 80617 60438 1 and NET WT 32 OZ (907g), UPC: 6 80617 60022 2
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1217-2019·2019-03-20

    Joy Gourmet Foods Recalls Idlee-Dosa Chutney Concentrate for Undeclared Sulfites

    Joy Gourmet Foods LLC is recalling Idlee-Dosa Chutney Fresh Concentrate because the product contains undeclared sulfites. The recall affects consumers in Connecticut, New York, and New Jersey.

    Product
    JOY IDLEE-DOSA Chutney FRESH CONCENTRATE NET WT 8 OZ (228g), UPC: 6 80617 60420 6
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0996-2019·2019-03-20

    Steris Recalls AMSCO 5000 Series Washer/Disinfector Units Due to Software Defect

    Steris Corporation is recalling 68 AMSCO 5000 Series Washer/Disinfector units because a software defect may prevent the intended cleaning cycle from processing, potentially leading to inadequate disinfection.

    Product
    AMSCO 5000 Series Washer/Disinfector Model # 5052
    Category
    Medical Device
    Distribution
    27 states
  • HighFDA (Devices)·Z-0993-2019·2019-03-20

    Durex Real Feel Condoms Recalled for Burst Pressure Failure

    Reckitt Benckiser LLC is recalling Durex Real Feel condoms because five batches failed burst pressure specifications.

    Product
    Durex Real Feel, synthetic polisoprene male condom, SKU 02340-89456-14 02340-89455-00 02340-89456-14 02340-89456-14 02340-89455-00 02340-95767-00 02340-89456-14 02340-89457-00 02340-89456-14 02340-89456-14 02340-89455-00 02340-89455-00 02340-95767-00 02340-95767-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·19730·2019-03-20

    Kubota Recalls Zero Turn Mowers Due to Fire Hazard

    Kubota is recalling about 3,850 zero turn mowers because the throttle cable can contact internal wiring, posing a fire hazard. No injuries have been reported.

    Product
    Kubota Zero Turn Mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1167-2019·2019-03-20

    Nature's Path Organic Chocolate Choco Chimps Cereal Recalled for Undeclared Gluten

    Nature's Path is recalling Organic Chocolate Choco Chimps cereal because it may contain undeclared gluten (wheat and barley).

    Product
    Nature's Path Organic Chocolate Choco Chimps Organic cereal. Net Wt. 10 oz (284 g), UPC 58449-87024. Nature's Path Foods, Inc., Blaine, WA 98230
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V214000·2019-03-20

    Fouts Bros Fire Apparatus Recall for Brake Light Wiring Defect

    Fouts Bros is recalling 2017-2018 F-3000, F-Rescue, and F-Pumper fire apparatus vehicles because brake lights may illuminate without the brake pedal being pressed.

    Product
    FOUTS BROS. — FOUTS BROS. F-PUMPER, F-3000, F-RESCUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0883-2019·2019-03-20

    King Bio Recalls Dr. King's SafeCare Rx Procrastination Due to Microbial Contamination

    King Bio Inc. is recalling 95 bottles of Dr. King's SafeCare Rx Procrastination because the product contains microbial contamination.

    Product
    Dr. King's SafeCare Rx Procrastination, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955276029, NDC 57955-2761-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1168-2019·2019-03-20

    Nature's Path Organic Gorilla Munch Corn Puffs Recalled for Undeclared Gluten

    Nature's Path is recalling Organic Gorilla Munch Corn Puffs cereal because it may contain undeclared gluten (wheat and barley). The recall covers 23,969 cases distributed nationwide and internationally.

    Product
    Nature's Path Organic Gorilla Munch Corn Puffs cereal. Net Wt. 10 oz (284 g), UPC 58449-86002. Nature's Path Foods, Inc., Blaine, WA 98230.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V215000·2019-03-20

    Thor Motor Coach Recalls 2018-2019 Quantum RW28 Motorhomes for Missing Lights

    Thor Motor Coach is recalling 2018-2019 Quantum RW28 motorhomes because they may be missing mid-ship marker lights, which can cause other drivers to underestimate the vehicle's length.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH QUANTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1218-2019·2019-03-20

    JOY Bhel Chutney Recalled for Undeclared Sulfites

    JOY Gourmet Foods LLC is recalling JOY Bhel Chutney because the product contains undeclared sulfites. The recall affects consumers in Connecticut, New York, and New Jersey.

    Product
    JOY Bhel Chutney NET WT 8 OZ (228g), UPC:6 80617 60433 6
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1221-2019·2019-03-20

    JOY Ginger Garlic Paste Recalled for Undeclared Sulfites

    JOY Gourmet Foods LLC is recalling specific sizes of Ginger Garlic Paste because the product contains undeclared sulfites. The recall affects products distributed in Connecticut, New York, and New Jersey.

    Product
    JOY Ginger Garlic Paste NET WT 8 OZ (228g), UPC:6 80617 60006 2 and NET WT 26 OZ (737g), UPC: 6 80617 60005 5
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0995-2019·2019-03-20

    Steris Recalls AMSCO 3000 Series Washer/Disinfector Units Due to Software Defect

    Steris Corporation is recalling 11 AMSCO 3000 Series Washer/Disinfector units because a software defect may prevent intended processing cycles, risking inadequate cleaning or damage to medical instruments.

    Product
    AMSCO 3000 Series Washer/Disinfector Model # 3052
    Category
    Medical Device
    Distribution
    27 states
  • HighFDA (Devices)·Z-0991-2019·2019-03-20

    Linet AVE 2 Birthing Bed Recalled for Power Cable Safety Issue

    Linet Spol. S.r.o. is recalling 253 AVE 2 Birthing Beds because the power cable may break or fail, posing a risk of sparks or exposure to live conductors.

    Product
    AVE 2 Birthing Bed
    Category
    Medical Device
    Distribution
    21 states
  • HighFDA (Food)·F-1156-2019·2019-03-20

    Finax Muesli Recalled for Unlabeled Hazelnut Allergen

    Chicago Importing Co is recalling Finax Muesli with Nuts and Fruit because the product was mislabeled and contains hazelnuts not listed on the label.

    Product
    Finax Muesli with Nuts and fruit 22.9-oz. Heat sealed plastic bag; 10 bags/case UPC: 7311142201402
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-1189-2019·2019-03-20

    Hikari Miso Recalled for Missing English Soy Allergen Labeling

    Hikari Miso International is recalling Hikari Enjuku Koji Miso Mutenka because the product lacks English labeling, failing to declare soy as an allergen.

    Product
    Hikari Enjuku Koji Miso Mutenka; 26.6 oz. plastic tub with lid. UPC 4 905663 003007
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1169-2019·2019-03-20

    Nature's Path Organic Cinnamon Jungle Munch Recalled for Undeclared Gluten

    Nature's Path is recalling Organic Cinnamon Jungle Munch cereal because it may contain undeclared gluten (wheat and barley).

    Product
    Nature's Path Organic Cinnamon Jungle Munch cereal. Net Wt. 10 oz (284 g), UPC 58449-87028. Nature's Path Foods, Inc., Blaine, WA 98230.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1183-2019·2019-03-20

    Golden Gate Soy Products Recalls Garden Gate Firm Tofu Due to Listeria

    Golden Gate Soy Products is recalling Garden Gate Firm Tofu after FDA sampling detected Listeria monocytogenes on food contact surfaces.

    Product
    Garden Gate Tofu, Firm; Ingredients: Soybean, Filter water, Calcium Sulfate. Contains: soy Sold in 60 piece (bulk box) and 18 piece packages 73 oz. - UPC 7 83301 96198 1 Pasteurized/Perishable. Keep Refrigerated. Made in USA.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1215-2019·2019-03-20

    Joy Gol-Gappa Masala Concentrate Recalled for Undeclared Sulfites

    Joy Gourmet Foods LLC is recalling Joy Gol-Gappa Masala Concentrate because it contains undeclared sulfites. The product was distributed in Connecticut, New York, and New Jersey.

    Product
    JOY GOL-GAPPA (PANI PURI) MASALA CONCENTRATE, NET WT 8 OZ (228g), UPC: 6 80617 60414 5
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0997-2019·2019-03-20

    Ossur Skull Pin Recall Due to Labeling Error and Safety Testing

    Ossur Americas is recalling 372 sterile titanium skull pins because the label incorrectly lists a ceramic tip and the products require confirmatory safety testing.

    Product
    Ossur Skull Pin, Sterile Titanium Pin, Part/Description: 516TS/ Skull Pin 2-1/4in TI Sterl 1PK; 516V2S/ Skull Pin 3in TI Sterl 1PK; 520TS/ Skull Pin 2-1/4in TI Sterl 5PK; 520V2S/ Skull Pin 3in TI Sterl 5 PK
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Food)·F-1213-2019·2019-03-20

    JOY Ginger Paste Recalled for Undeclared Sulfites

    JOY Gourmet Foods LLC is recalling JOY Ginger Paste in 8 oz and 26 oz sizes because the product contains undeclared sulfites.

    Product
    JOY Ginger Paste NET WT 26 OZ (737g), UPC: 6 80617 60001 7 and NET WT 8 OZ (228g), UPC: 6 80617 60002 4
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1001-2019·2019-03-20

    Ossur Halo System Ring Kits Recalled for Labeling and Safety Testing

    Ossur Americas is recalling 182 units of Halo system ring kits due to a labeling error and the need for confirmatory safety testing.

    Product
    Ossur, Sterile, Part/ Description: 505300T/ CB RING KIT TI SM; 505300V2/ OB V2 RING KIT TI SM; 505400T/ CB RING KIT TI STD; 505400V2/ OB V2 RING KIT TI STD; 505500T/ CB RING KIT TI LG; 505500V2/ OB V2 RING KIT TI LG; 515300V2/ OB V2 RING KIT TI SM-No App; 515400V2/ OB
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Food)·F-1157-2019·2019-03-20

    Kradjian Importing Recalls Zarrin Pickled Cucumbers Due to Leaking Cans

    Kradjian Importing Co is recalling Zarrin Pickled Cucumbers & Cornichons because some cans are leaking and swollen. Consumers should stop using the product.

    Product
    Zarrin Pickled Cucumbers & Cornichons: Net Weight 101.4 oz. 3 kg. Ingredients: Cucumber, water, salt, acid (acetic acid, spices, food coloring (tartrazine). Refrigerate after opening. UPC 7 64363 18305 2 Product of the West Bank Packed for Blanish International, PO Box 2
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Food)·F-1219-2019·2019-03-20

    JOY Chat Chutney Recalled for Undeclared Sulfites

    JOY Gourmet Foods LLC is recalling JOY Chat Chutney because it contains undeclared sulfites. The product was distributed in Connecticut, New York, and New Jersey.

    Product
    JOY Chat Chutney NET WT 8 OZ (228g), UPC:6 80617 60408 4
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1220-2019·2019-03-20

    JOY Coriander Chutney Recalled for Undeclared Sulfites

    JOY Gourmet Foods LLC is recalling specific sizes of Coriander Chutney because the product contains undeclared sulfites.

    Product
    JOY Coriander Chutney NET WT 8 OZ (228g), UPC:6 80617 60402 2 and NET WT 26 OZ (737g), UPC: 6 80617 60401 5
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1214-2019·2019-03-20

    JOY Garlic Paste Recalled for Undeclared Sulfites

    JOY Gourmet Foods LLC is recalling specific jars of garlic paste because they contain undeclared sulfites. Consumers in Connecticut, New York, and New Jersey should check their pantries.

    Product
    JOY Garlic Paste NET WT 26 OZ (737 g) UPC: 6 80617 60003 1 and NET WT 8 OZ (228g) UPC: 6 80617 60004 8
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1158-2019·2019-03-20

    Kradjian Imports Recalls Leaking and Swollen Bulgarian White Brined Sheep's Milk Cheese

    Kradjian Imports Co. is recalling 952 cases of Bulgarian White Brined Sheep's Milk cheese due to leaking and swollen cans. The product was distributed across 14 states.

    Product
    Bulgarian White Brined Sheep's Milk cheese; 5 gallon can Ingredients: Pasteurized Sheep's Milk, Bacterial culture, salt, rennet. Product of Belgium. Imported by Kradjian Imports Co., Inc., Glendale, CA 91204
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-1008-2019·2019-03-20

    Olympus GIF-H180J Gastrointestinal Videoscope Recalled Due to Adhesive Error

    Olympus is recalling one GIF-H180J videoscope because the adhesive used for its repair was incorrectly prepared, potentially affecting the device's durability.

    Product
    Olympus GIF-H180J Gastrointestinal Videoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1012-2019·2019-03-20

    Medtech Recalls Little Remedies New Baby Essentials Kit for Labeling Errors

    Medtech Products is recalling 4,716 Little Remedies New Baby Essentials Kits because the cartons contain incorrect labeling for two of the five items inside.

    Product
    Little Remedies New Baby Essentials Kit. Each kit contains 1 each of the following products: Little Remedies Infant Fever Reducer (acetaminophen 150mg) 2 fl. oz. bottle, Little Remedies Saline Spray/Drops (sodium chloride) 0.5 fl oz., Little Remedies Gripe Water (zingiber officin
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0996-2019·2019-03-20

    Lannett Recalls Oxybutynin Chloride Tablets for Dissolution Failures

    Lannett Company Inc. is recalling 14,448 bottles of Oxybutynin Chloride Extended-Release Tablets because they failed to meet dissolution specifications.

    Product
    OXYBUTYNIN CHLORIDE — OXYBUTYNIN CHLORIDE (OXYBUTYNIN CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1005-2019·2019-03-20

    Zimmer NexGen Trabecular Metal Tibial Augment Recall for Label Mismatch

    Zimmer Trabecular Metal Technology is recalling 24 units of NexGen Tibial Half Block Augments because the product in the box may not match the label.

    Product
    NexGenTrabecular Metal Tibial Half Block Augment, Right Lateral/Left Medial, Size 4 5MM Thickness W/Screws Item Number: 00544800426 Product Usage: The Trabecular Metal Tibial Cone Augments are intended for use where severe degeneration, trauma, or other pathology of the kne
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0999-2019·2019-03-20

    Ossur OB Resolve Sterile Ring Kits Recalled for Labeling Errors

    Ossur Americas is recalling 342 units of OB Resolve sterile ring kits due to a labeling error on titanium pins and pending safety testing.

    Product
    Ossur OB Resolve, Sterile, Part/ Description: 505300D/ OB RESOLVE STERILE RING SML; 505400D/ OB RESOLVE RING KIT STD; 505500D/ OB RESOLVE RING KIT LRG; 515300D/ OB RESOLVE RING KIT SM-No App; 515400D/ OB RESOLVE RING KIT STD-No App; 515500D/ OB RESOLVE RING KIT LG-No Ap
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-1009-2019·2019-03-20

    Olympus PCF-Q180AC Video Colonoscope Recalled Due to Adhesive Error

    Olympus is recalling two video colonoscopes because the adhesive used in their repair was incorrectly prepared, potentially affecting the durability of the repair.

    Product
    Olympus PCF-Q180AC Video Colonoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1010-2019·2019-03-20

    Olympus TJF-Q180V Duodenoscope Recalled Due to Adhesive Preparation Error

    Olympus is recalling two TJF-Q180V duodenoscopes because the adhesive used in their repair was incorrectly prepared, potentially affecting the device's durability or effectiveness.

    Product
    Olympus TJF-Q180V Duodenoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1004-2019·2019-03-20

    Macleods Pharma Recalls Telmisartan and Hydrochlorothiazide Tablets for Blend Uniformity

    Macleods Pharma USA is recalling Telmisartan and Hydrochlorothiazide tablets because they failed blend uniformity specifications. The recall covers 140,589 bottles distributed nationwide.

    Product
    Telmisartan and Hyrdochlorothiazide Tablets, USP 80mg/12.5 mg, 30-coun bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals Ltd. Baddi, Imachal Pradesh, India NDC 33342-129-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1007-2019·2019-03-20

    Olympus Ultrasound Gastrovideoscope Recalled Due to Adhesive Preparation Error

    Olympus is recalling one ultrasound gastrovideoscope because the adhesive used for its repair was incorrectly prepared, potentially affecting the device's durability.

    Product
    Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1003-2019·2019-03-20

    Ossur ReSolve Halo Vest Recalled for Labeling and Safety Testing Issues

    Ossur Americas is recalling 381 ReSolve Halo Vests because the titanium pin label incorrectly lists a ceramic tip and the products require confirmatory safety testing.

    Product
    Ossur, ReSolve Halo Vest, Part/ Description: 545700K/ ReSolve Halo Vest-shrt kodel; 545700L/ ReSolve Halo Vest-shrt lmbwool; 545800K/ ReSolve Halo Vest-tall kodel; 545800L/ ReSolve Halo Vest-tall lmbwool
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-1000-2019·2019-03-20

    Ossur CB Resolve Halo System Recalled for Labeling and Testing Issues

    Ossur Americas is recalling 656 units of CB Resolve Halo system products due to a labeling error and the need for confirmatory safety testing.

    Product
    Ossur CB Resolve, Sterile, Part/ Description: 505300C/ CB RESOLVE STERILE UNIT SML; 505400C/ CB RESOLVE STERILE UNIT STD; 505500C/ CB Resolve Sterile Unit LRG; 515300C/ CB RESOLVE RING KIT SM-No App; 515400C/ CB RESOLVE RING KIT STD-No App; 515500C/ CB RESOLVE RING KIT
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-1004-2019·2019-03-20

    Ossur LIL Angel Vest Recalled for Labeling and Safety Testing Issues

    Ossur Americas is recalling 45 LIL Angel Vests because the titanium pin labels incorrectly list ceramic tips and require confirmatory safety testing.

    Product
    Ossur, LIL Angel Vest, Part/ Description: 545100K/ LIL ANGEL VEST P2 KODEL; 545100L/ LIL ANGEL VEST P2 LAMBSWOOL; 545100S/ LIL ANGEL VEST P2 SORBATEX; 545150K/ LIL ANGEL VEST P3 KODEL; 545150L/ LIL ANGEL VEST P3 LAMBSWOOL; 545150S/ LIL ANGEL VEST P3 SORBATEX
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-0998-2019·2019-03-20

    Ossur Skull Pin Recall for Labeling Error and Safety Testing

    Ossur Americas is recalling 824 sterile skull pins due to a label error and pending safety testing.

    Product
    Ossur Skull Pin, Sterile Ceramic Tip Pin, Part/ Description: 516CS/ Skull Pin 2-1/4in CT Sterl 1PK; 516DS/ Skull Pin 3in CT Sterl 1PK; 517CS/ Skull Pin 2-1/4in CT Sterl 4PK; 517DS/ Skull Pin 3in CT Sterl 4 PK; 522CS/ Skull Pin 2-1/4in CT Sterl 6PK; 522C/ SKULL PIN 2-1/4
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-1002-2019·2019-03-20

    Ossur J Tong Sterile Medical Device Recall for Labeling Error

    Ossur Americas is recalling 138 units of J Tong sterile medical devices because the titanium pin label incorrectly lists a ceramic tip.

    Product
    Ossur, J Tong, Sterile, Part/ Description: JT-115/ J TONG MED/LGE-No App; JT-200/ J TONG ASSEMBLY SML/MED; JT-210/ J TONG ONLY SML/MED; JT-400/ J TONG COMPONENT TRAY
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Drugs)·D-1005-2019·2019-03-20

    Macleods Pharma Recalls Telmisartan and Hydrochlorothiazide Tablets for Blend Uniformity

    Macleods Pharma USA is recalling Telmisartan and Hydrochlorothiazide tablets because they failed content uniformity specifications for blend uniformity.

    Product
    Telmisartan and Hyrdochlorothiazide Tablets 80 mg/25 mg, 30-count bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals Ltd. Baddi Himachal Pradesh, INDIA, NDC 33342-130-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1003-2019·2019-03-20

    Macleods Pharma Recalls Telmisartan and Hydrochlorothiazide Tablets for Blend Uniformity

    Macleods Pharma USA is recalling Telmisartan and Hydrochlorothiazide tablets because they failed blend uniformity specifications.

    Product
    Telmisartan and Hyrdochlorothiazide Tablets 40mg/12.5 mg, 30-count bottles, Rx Only, Manufactured for:Macleods Pharma USA, Inc. Plainsboro, NJ 08536, Manufactured for: Macleods Pharmaceuticals Ltd. Baddi, Himchal Pradesh INDIA, NDC 33342-128-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0979-2019·2019-03-20

    Cook Transseptal Needle Recalled for Missing Back Bevel

    Cook Inc. is recalling 100 units of Transseptal Needles manufactured without a back bevel on the needle tip, which could damage the introducer during insertion.

    Product
    Cook Transseptal Needle, Reference Number TSNC-18-71.0, Order Number G02364. For transseptal left heart access in both diagnostic and interventional procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0991-2019·2019-03-20

    Boehringer Ingelheim Recalls Mirapex Tablets Due to Low Weight

    Boehringer Ingelheim is recalling 112 cartons of Mirapex 1 mg tablets because routine stability testing identified low-weight tablets.

    Product
    Mirapex (pramipexole dihydrochloride) Tablets, 1 mg, 100-count unit-dose tablets per folding carton, Rx only, Distributed by: Boehringer Ingelheim (BI) Pharmaceuticals, Inc., Ridgefield, CT 06877 USA, Made in Germany, NDC 0597-0190-61.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·033-2019·2019-03-19

    La Rosita Fresh Market Recalls Ground Beef for E. coli O157:H7

    La Rosita Fresh Market in Mt. Prospect, Illinois, is recalling raw ground beef products due to possible E. coli O157:H7 contamination.

    Product
    La Rosita Fresh Market Inc. Recalls Ground Beef Products due to Possible E. coli O157:H7 Contamination
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·19V212000·2019-03-19

    Alexis Fire Equipment Recalls 2018 Fire Apparatus Due to Brake Light Defect

    Alexis Fire Equipment is recalling 11 units of 2018 Custom Fire Apparatus because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.

    Product
    ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V211000·2019-03-19

    Collins Recalls 2015-2019 School Buses Due to Barrier Restraint Defect

    Collins Bus is recalling 2015-2019 school buses because a specific barrier may fail to restrain unbelted occupants during a crash, increasing injury risk.

    Product
    COLLINS — COLLINS DH400, DH516, DE500, DE416
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V206000·2019-03-18

    Keystone Recalls 2019 Dutchmen Trailers Due to Cooktop Burn Hazard

    Keystone RV is recalling 2019 Dutchmen Coleman and Aspen Trail trailers because the cooktop may cause excessive heat buildup and burns when the furnace is on.

    Product
    DUTCHMEN — DUTCHMEN COLEMAN, ASPEN TRAIL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V209000·2019-03-18

    Mack Trucks Recalls 2020 Models Due to Blocked Rear Reflectors

    Mack Trucks is recalling 2020 Anthem and Pinnacle trucks because exhaust systems may block rear reflectors, reducing vehicle visibility.

    Product
    MACK — MACK ANTHEM (AN), PINNACLE (PI/PN), PINNACLE (CHU), PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·032-2019·2019-03-15

    Procesadora La Hacienda Recalls Corned Beef Due to Metal Contamination

    Procesadora La Hacienda is recalling approximately 4,940 pounds of ready-to-eat corned beef products that may contain pieces of metal. The products were distributed to institutions in Puerto Rico.

    Product
    Procesadora La Hacienda, Inc. — Procesadora La Hacienda, Inc. Recalls Beef Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·19V200000·2019-03-14

    Thor Motor Coach Recalls 2018-2019 Aria and Palazzo Motorhomes

    Thor Motor Coach is recalling 2018-2019 Aria and 2019 Palazzo motorhomes because loose steering and tie rod arm bolts may separate, increasing crash risk.

    Product
    THOR — THOR PALAZZO, ARIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·031-2019·2019-03-14

    Breaded Chicken Patties Recalled for Possible Metal Contamination

    Productos La Aguadillana, Inc. is recalling breaded chicken patties that may contain pieces of metal. The products were shipped to institutions in Puerto Rico.

    Product
    Productos La Aguadillana, Inc. — Productos La Aguadillana, Inc. Recalls Breaded Chicken Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·19V201000·2019-03-14

    Chrysler Recalls 2019 Jeep Wrangler and Ram 1500 for Steering Defect

    Chrysler is recalling 2019 Jeep Wrangler and Ram 1500 vehicles because improperly machined steering column stub shafts may break, potentially causing the steering wheel to detach.

    Product
    RAM — RAM, JEEP 1500, WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19728·2019-03-14

    Kawasaki Recalls Mule Pro-MX Utility Vehicles Due to Fuel Leak Fire Hazard

    Kawasaki is recalling about 2,600 Mule Pro-MX off-highway utility vehicles because oil cooler hoses and fuel tank cap gaskets can fail, causing fuel leaks and fire hazards.

    Product
    Kawasaki Mule™ Pro-MX™ off-highway utility vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V204000·2019-03-14

    Hyundai Recalls 2013 Veloster Vehicles Due to Engine Software Defect

    Hyundai is recalling 2013 Veloster vehicles with 1.6-liter turbo engines because software may cause premature ignition, risking engine damage, fire, or stalling.

    Product
    HYUNDAI — HYUNDAI VELOSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19082·2019-03-14

    Tech Gear 5.7 Recalls Heated Socks Due to Fire and Burn Hazards

    Tech Gear 5.7 is recalling Mobile Warming Performance Heated Socks because the lithium-ion battery can overheat, melt, or ignite, posing fire and burn risks.

    Product
    Mobile Warming Performance Heated Socks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V203000·2019-03-14

    Chrysler Recalls 2019 Models for Instrument Cluster Illumination Defect

    Chrysler is recalling 2019 Dodge Challenger, Charger, and Chrysler 300 vehicles because the instrument cluster may fail to illuminate driver warnings, increasing crash risk.

    Product
    CHRYSLER — CHRYSLER, DODGE 300, CHARGER, CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19083·2019-03-14

    O'Brien Performer Pro Combo Water Skis Recalled for Injury Hazard

    O'Brien Watersports is recalling Performer Pro Combo water skis because the bindings can detach during falls, causing the skis to break and injure users.

    Product
    Performer Pro Combo water skis
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19081·2019-03-14

    Brush Art Recalls WIC Nutrition Plates Due to Fire Hazard

    Brush Art is recalling WIC nutrition plates because they contain aluminum and are incorrectly labeled as microwave-safe, posing a fire hazard.

    Product
    WIC nutrition plates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V202000·2019-03-14

    Forest River Recalls 2018-2019 Motorhomes and Buses for Reversed Camera Image

    Forest River is recalling 2018-2019 motorhomes, work trucks, and shuttle buses because backup camera images may display in reverse, increasing crash risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS, FOREST RIVER, COACHMEN ALLSTAR, BERKSHIRE, FREELANDER, ORION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·030-2019·2019-03-13

    Butterball Recalls Raw Ground Turkey Due to Salmonella Schwarzengrund Contamination

    Butterball is recalling approximately 78,164 pounds of raw ground turkey products due to possible Salmonella Schwarzengrund contamination. The products were shipped to retail and institutional locations nationwide.

    Product
    Butterball, LLC — Butterball LLC Recalls Turkey Products Due to Possible Salmonella Schwarzengrund Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1139-2019·2019-03-13

    Whole Foods Hipster Chipster Cookies Recalled for Undeclared Walnuts

    Whole Foods Market is recalling Hipster Chipster Cookies sold in Santa Rosa, CA, due to undeclared walnuts that caused an anaphylactic reaction.

    Product
    Whole Foods Hipster Chipster Cookies; 9 oz. container with 6 cookies; UPC 0247449 006990 Sold at Whole Foods, Yulupa Ave., Santa Rosa, CA
    Category
    Food
    Distribution
    0 states

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