Archive
1,183 recalls were announced in July 2015.
Of the 1,183 recalls this month scored against our rubric, 29% are Critical, 19% are Severe.
Which agencies issued them
Boba Direct, Inc. is recalling strawberry flavored bubble tea powder because it contains undeclared allergens. The product was distributed in five states.
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.
Stradis Healthcare is recalling Basic Packs containing Devon Light Gloves because the manufacturer, Medtronic, is recalling the glove component.
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.
Boba Direct, Inc. is recalling red bean flavored powder due to undeclared allergens. The product was distributed in Illinois, Missouri, Ohio, Florida, and Tennessee.
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.
Boba Direct, Inc. is recalling taro flavored powder due to undeclared allergens. The product was distributed in five US states.
Specialized Bicycle Components is recalling about 6,500 Pedal Axle Extenders because they can break, causing riders to lose control and fall.
Paradigm Foodworks is recalling The Hungry Dragon Original Flavor Stir Fry Marinade BBQ Sauce due to potential peanut protein contamination.
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.
Stradis Healthcare is recalling Arthroscopy Packs because they contain Devon Light Gloves, which are being recalled by the manufacturer Medtronic.
Paradigm Foodworks is recalling Hazelwood's All Natural Mild Salsa due to potential contamination with peanut protein.
FDA is recalling Shiley Neonatal and Pediatric Tracheostomy Tubes because patients reported discomfort and breathing difficulties after switching to these products.
BTE Technologies is recalling 510 Primus rehabilitation devices because the optional Chop / Lift Bar may detach, posing a fall hazard to users.
Boba Direct, Inc. is recalling chocolate flavored powder for bubble tea due to undeclared allergens. The product was distributed in five states.
Boba Direct, Inc. is recalling honeydew flavored bubble tea powder because it contains undeclared allergens. The product was distributed in five US states.
Boba Direct, Inc. is recalling vanilla bubble tea powder sold in foil bags due to undeclared allergens. The product was distributed in five states.
Boba Direct, Inc. is recalling matcha green tea flavored powder in 2.2 lb foil bags because the product contains undeclared allergens.
Stradis Healthcare is recalling nine Breast Packs containing Devon Light Gloves due to a manufacturer recall of the glove component.
Boba Direct, Inc. is recalling milk tea flavored powder due to undeclared allergens. The product was distributed in five US states.
Boba Direct, Inc. is recalling banana flavored powder in foil bags because the product contains undeclared allergens.
Boba Direct, Inc. is recalling green tea flavored powder due to undeclared allergens. The product was distributed in five US states.
Paradigm Foodworks is recalling Soog Head Hot Pineapple Smash Salsa due to potential contamination with peanut protein.
Boba Direct, Inc. is recalling lavender flavored powder due to undeclared allergens. The product was distributed in five US states.
Boba Direct, Inc. is recalling passion fruit flavored powder due to undeclared allergens. The product was distributed in five states.
Boba Direct, Inc. is recalling watermelon flavored powder due to undeclared allergens. The product was distributed in five US states.
Boba Direct, Inc. is recalling cafe latte flavored powder for containing undeclared allergens. The product was distributed in five states.
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.
Aspen Foods is recalling approximately 1.98 million pounds of frozen, raw, stuffed, and breaded chicken products due to possible Salmonella Enteritidis contamination linked to illnesses in Minnesota.
Paradigm Foodworks is recalling Soog Head Mild Pineapple Smash Salsa due to potential contamination with peanut protein.
Boba Direct, Inc. is recalling almond flavored powder due to undeclared allergens. The product was distributed in five states.
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.
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.
Paradigm Foodworks is recalling Hazelwood's Cilantro Salsa due to potential peanut protein contamination. Consumers should check their pantry for the specific lot code.
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.
Southern Style Spices is recalling 775 lbs of ground cumin distributed in Texas because it may contain peanut protein.
Vermeer is recalling 2012-2015 BC900XL brush chippers because flanges may crack, causing the discharge chute to separate and create a road hazard.
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.
New Punjab Sweets Inc. is voluntarily recalling Rosgula snacks due to undeclared almonds, colors, and wheat.
New Punjab Sweets Inc. is voluntarily recalling Kaju Katri Indian snacks because they may contain undeclared cashews and artificial colors Yellow 5 and 6.
Stradis Healthcare is recalling Neurosurgery Packs because they contain Devon Light Gloves that are subject to a separate recall by Medtronic.
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.
New Punjab Sweets Inc. is voluntarily recalling New Punjab Burfi because the Indian snack may contain undeclared almonds, pistachios, and cashews.
Paradigm Foodworks is recalling Hazelwood's Habanero Salsa due to potential peanut contamination. The product was distributed in four US states and Ontario, Canada.
Bedessee Imports is recalling Brown Betty Coconut Milk Powder Mix because it contains sodium caseinate but lacks a milk declaration.
Paradigm Foodworks is recalling Rub with Love Ancho & Molasses Barbecue Sauce due to potential peanut protein 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.
Paradigm Foodworks is recalling Soog Head Medium Pineapple Smash Salsa due to potential peanut protein contamination.
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.
Paradigm Foodworks is recalling D.A.M. brand Hot Salsa due to potential contamination with peanut protein.
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.
Boba Direct, Inc. is recalling cherry flavored powder in foil bags due to undeclared allergens. The product was distributed in five states.
Paradigm Foodworks is recalling Traeger brand Chili Barbecue Sauce due to potential contamination with peanut protein.
Boba Direct, Inc. is recalling blueberry flavored powder due to undeclared allergens. The product was distributed in five US states.
New Punjab Sweets Inc. is voluntarily recalling Kaju Fry (toasted fried cashews) because the product may contain undeclared cashew nuts.
New Punjab Sweets Inc. is voluntarily recalling Chum Chum snacks due to undeclared almonds, coconut, wheat, and food colors.
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.
Bexco is recalling DaVinci brand cribs because a metal bracket can break, creating gaps that pose entrapment, fall, and laceration risks to infants.
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.
Lifeline Systems is recalling 38 Philips GoSafe Communicator 7000L units because they may fail to sense the phone line under unusual landline conditions.
Boba Direct, Inc. is recalling coconut flavored powder due to undeclared allergens. The product was distributed in five US states.
Paradigm Foodworks is recalling Hungry Dragon Extra Spicy Stir Fry Marinade BBQ Sauce due to potential peanut protein contamination.
New Punjab Sweets Inc. is voluntarily recalling Ladoo snacks because they lack an ingredient label and may contain undeclared nuts, colors, and wheat.
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.
New Punjab Sweets Inc. is voluntarily recalling Kaju Roll snacks because they may contain undeclared cashews and artificial colors Yellow 5 and 6.
Spartan is recalling 2007-2015 emergency response vehicles because front wheel valve stems may rub against brake calipers, causing sudden tire deflation.
Boba Direct, Inc. is recalling spiced chai flavored powder because it contains undeclared allergens. The product was distributed in five US states.
Avon is recalling approximately 27,000 nut choppers because the grinding mechanism's tines can break and fall into food, posing a risk of injury.
Boba Direct, Inc. is recalling lychee flavored powder due to undeclared allergens. The product was distributed in five US states.
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.
Stradis Healthcare is recalling Suction Packs containing Devon Light Gloves because the manufacturer, Medtronic, recalled the glove component.
Stradis Healthcare is recalling Knee Arthro Packs because they contain a Devon Light Glove component that Medtronic is recalling.
Stradis Healthcare is recalling Standard Packs containing Devon Light Gloves because the glove component was recalled by Medtronic.
Stradis Healthcare is recalling Eye Packs containing Devon Light Gloves due to a manufacturer recall of the glove component by Medtronic.
Stradis Healthcare is recalling Vaginal Rejuvenation Packs because they contain a Devon Light Glove component that Medtronic is recalling.
Stradis Healthcare is recalling three Laser Evlt Packs and Laser One Leg Evlt kits because they contain a Devon Light Glove component recalled by Medtronic.
American Health Packaging is recalling 5,591 cartons of Lisinopril 20mg tablets nationwide because the firm did not adequately investigate customer complaints.
Stradis Healthcare is recalling Orthopedic Split Drape Packs because they contain a Devon Light Glove component recalled by Medtronic.
American Health Packaging is recalling Amlodipine besylate tablets 5mg due to CGMP deviations involving inadequate investigation of customer complaints.
American Health Packaging is recalling 13,532 cartons of Lisinopril 10mg tablets because the firm did not adequately investigate customer complaints.
Stradis Healthcare is recalling Bariatric Packs because they contain Devon Light Gloves that are subject to a separate manufacturer recall by Medtronic.
Mylan Pharmaceuticals is recalling 1,068 bottles of Capecitabine Tablets, 500 mg, because the product failed to meet dissolution specifications.
Synthes is recalling three units of a titanium end cap for tibial nails because they were shipped before a required internal inspection was completed.
Stradis Healthcare is recalling Custom Packs containing Devon Light Gloves due to a manufacturer recall of the glove component by Medtronic.
American Health Packaging is recalling Lisinopril tablets 40mg due to inadequate investigation of customer complaints. The recall covers 1,516 cartons distributed nationwide.
Stradis Healthcare is recalling Head & Neck Packs containing Devon Light Gloves due to a manufacturer recall of the glove component.
American Health Packaging is recalling 4,718 cartons of Lisinopril 5mg tablets due to inadequate investigation of customer complaints.
American Health Packaging is recalling 2,068 cartons of Azithromycin tablets 250mg due to inadequate investigation of customer complaints.
Stradis Healthcare is recalling breast augmentation kits because they contain Devon Light Gloves, which are being recalled by the manufacturer Medtronic.
Stradis Healthcare is recalling Lipo Packs, Expended Packs, and Trays because they contain Devon Light Gloves that Medtronic is recalling.
Apotex Inc. is recalling 4,584 bottles of Enalapril maleate and hydrochlorothiazide tablets, 10/25 mg, because the product may not meet blend uniformity specifications.
Stradis Healthcare is recalling surgical shoulder packs because they contain Devon Light Gloves that are subject to a separate manufacturer recall by Medtronic.
American Health Packaging is recalling 3,572 cartons of Clarithromycin tablets, USP 500mg, because the firm did not adequately investigate customer complaints.
Stradis Healthcare is recalling surgical hand packs because they contain Devon Light Gloves, a component recalled by manufacturer Medtronic.
Stradis Healthcare is recalling DND Packs containing Devon Light Gloves because the glove manufacturer, Medtronic, is recalling the component.
Stradis Healthcare is recalling surgical and general surgery packs because they contain Devon Light Gloves, a component being recalled by Medtronic.
Stradis Healthcare is recalling surgical Set Up Packs because they contain Devon Light Gloves that Medtronic is recalling.
American Health Packaging is recalling 838 cartons of Azithromycin 600mg tablets because the firm did not adequately investigate customer complaints.
Stradis Healthcare is recalling Blepharoplasty Packs because they contain Devon Light Gloves, which are subject to a separate recall by Medtronic.
Stradis Healthcare is recalling ENT Packs containing Devon Light Gloves due to a manufacturer recall of the glove component.
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