Archive
629 recalls were announced in November 2017.
Of the 629 recalls this month scored against our rubric, 11% are Critical, 27% are Severe.
Which agencies issued them
Purdue Pharma is recalling Betadine Povidone-Iodine swabsticks because a manufacturing error caused the product to be subpotent.
Mann Packing Company is recalling Mann's Fiesta Vegetable Tray after a sample tested positive for Listeria monocytogenes.
Mann Packing Company is recalling specific Mann's and Signature Farms hummus trays after a sample tested positive for Listeria monocytogenes.
Mann Packing Company is recalling specific bags of chopped cauliflower after testing detected Listeria monocytogenes. Consumers should check their freezers for the affected products.
Albertsons Inc is recalling Premium Vegetable Trays sold in Albertson's and Safeway stores because they were made with product recalled for potential Listeria monocytogenes.
Mann Packing Company is recalling specific trays of Mann's Nourish Bowls Butternut Kale Risotto because a sample tested positive for Listeria monocytogenes.
The Kroger Co is recalling 543 kits of Asian Pasta Salad because the product may be contaminated with Listeria monocytogenes. The recall affects stores in Colorado, New Mexico, Utah, and Wyoming.
Mann Packing Company is recalling Mann's Broccoli Cole Slaw because a sample tested positive for Listeria monocytogenes. Consumers should discard the product.
Mann Packing Company is recalling Cross Valley Farms Spiral Cut Kohlrabi because a sample tested positive for Listeria monocytogenes.
Mann Packing Company is recalling Archer Farms Broccoli Medley 12 oz bags due to a positive Listeria monocytogenes test result.
Albertsons is recalling 8-ounce Veggies w/ Dip trays sold in several states because they were made with product recalled for potential Listeria monocytogenes.
Mann Packing Company is recalling HEB Shaved Brussels Sprouts Salad because a sample tested positive for Listeria monocytogenes.
Albertsons is recalling 14-ounce broccoli and cauliflower trays sold in select states because they were made with product recalled for potential Listeria monocytogenes.
Mann Packing Company is recalling specific lots of Mann's Nourish Bowls Bacon Maple Brussels due to a positive test for Listeria monocytogenes.
Mann Packing Company is recalling specific 12 oz. bags of Mann's Family Favorites Broccoli Carrots and HEB brand products due to a positive Listeria monocytogenes test.
Mann Packing Company is recalling Mann's Family Favorites California Stir Fry because a sample tested positive for Listeria monocytogenes.
Mann Packing Company is recalling Western Family Kale Salad Kits after FDA sampling detected Listeria monocytogenes.
Mann Packing Company is recalling Signature Farms Meat & Cheese Trays because a related salad product tested positive for Listeria monocytogenes.
Mann Packing Company is recalling specific trays of Mann's Snacking Favorites Honey Turkey Cheddar because a sample tested positive for Listeria monocytogenes.
Mann Packing Company is recalling specific veggie trays due to a positive Listeria monocytogenes test result.
Mann Packing Company is recalling Mann's Vegetable Tray products due to a positive test for Listeria monocytogenes. Consumers should discard the product or return it to the store.
Mann Packing Company is recalling HEB Fiesta Salad because FDA sampling detected Listeria monocytogenes. Consumers should not eat the product.
Windstone Medical Packaging is recalling 60 custom surgical kits containing a recalled catheter component due to a potential sterile barrier breach.
Mann Packing Company is recalling specific bags of Shaved Brussels Sprouts because FDA sampling detected Listeria monocytogenes.
Mann Packing Company is recalling Mann's Power Blend salad due to a positive test for Listeria monocytogenes. Consumers should discard the product.
Mann Packing Company is recalling specific trays of Mann's Snacking Favorites Cheddar Pretzel Veggie Tray because a sample tested positive for Listeria monocytogenes.
Mann Packing Company is recalling Mann's Nourish Bowl Monterey Risotto because a CFIA sample tested positive for Listeria monocytogenes.
Mann Packing Company is recalling Western Family Spicy Southwester Kale Kit due to a positive Listeria monocytogenes test result.
Mann Packing Company is recalling Mann's Rainbow Salad after a sample tested positive for Listeria monocytogenes. The affected 12 oz bags were distributed in the US and Canada.
Mann Packing Company is recalling specific bags of Brussels sprouts after a sample tested positive for Listeria monocytogenes.
Toyota is recalling 2012-2015 Prius Plug-in Hybrids because a fuse may fracture, causing power loss and increasing crash risk.
Sorin Group USA is recalling a specific lot of FlexFlow Venous Cannulas because they are sharper or pointier than expected.
Epimed International is recalling 263 units of TUOHY Epidural Needles because a partially incomplete seal could impact the product's sterility.
North Star Imaging is recalling three Model X-7000 industrial cabinet x-ray systems due to a discovered low-level radiation leak.
New American Food Products is recalling specific dark chocolate covered ginger products because they contain undeclared milk.
E & E Enterprises is recalling Muriel's Cheesey Bacon Dip because the label failed to declare milk and specific FD&C colors.
Mann Packing Company is recalling 12 oz bags of Broccoli Slaw sold in the US and Canada because a sample tested positive for Listeria monocytogenes.
Terumo BCT is recalling 525 Harvest Graft Delivery Packs because some lots may lack a seal on the inner pouch, potentially compromising sterility.
Wholesale Fireworks is recalling Toxic artillery rockets, Boom Box aerial shells, and Detonator firecrackers due to federal standard violations that pose explosion and burn hazards.
Stonyfield Farm is recalling 17,688 cups of Organic O'soy Strawberry on the Bottom Soy Yogurt because the product may contain undeclared milk.
Bush Hog is recalling about 500 HDE riding lawn mowers because the blade can separate from the spindle, posing a laceration hazard.
Boston Scientific is recalling 12 Resonate EL ICD DR devices due to incorrect firmware configuration. The devices were distributed to medical facilities in Minnesota and Ohio.
New American Food Products is recalling Market Basket Dark Chocolate Almonds because the product contains undeclared milk.
Encore Medical is recalling 840 units of Cobalt MV Bone Cement because the sterile Tyvek packaging seal may be lost, potentially compromising sterility.
BMW is recalling 3,188 2018 vehicles because a software error may prevent the instrument panel from illuminating, increasing crash risk.
Giant Eagle is recalling Market District Powerberry Mix Covered in Dark Chocolate due to undeclared milk in the dark chocolate.
Toyota is recalling 2018 C-HR vehicles because the electronic parking brake may fail to engage or disengage, increasing the risk of vehicle rollaway.
Zimmer Biomet is recalling a custom titanium knee implant because it contained a nickel-containing screw, posing a risk to a patient with a nickel allergy.
New American Food Products is recalling specific dark chocolate covered berry products because they contain undeclared milk.
New American Food Products is recalling dark chocolate espresso beans sold at various retailers because they contain undeclared milk.
Giant Eagle is recalling Market District Almonds Covered in Dark Chocolate due to undeclared milk. The product is distributed in five states.
Teleflex Medical is recalling 13,710 units of the Auto Endo5 Automatic Hem-o-lok Clip Applier because clips may misalign, jam, or fall out of the device.
E & E Enterprises is recalling Muriel's Cheesey Pizza Dip because the label fails to declare milk and specific FD&C colors.
21st Century Snack Foods is recalling Dark Chocolate Almonds because the product contains undeclared milk, a major food allergen.
Encore Medical, Lp is recalling Cobalt HV with Gentamicin bone cement because the sterile Tyvek packaging may have lost its seal, potentially compromising sterility.
Epimed International is recalling 500 units of RX-2 COUDE Epidural Needles due to a potential incomplete seal that may impact sterility.
Albertsons is recalling 72-ounce vegetable trays sold in several states because they were made with product recalled for potential Listeria monocytogenes.
Giant Eagle is recalling Market District Coffee Beans Covered in Dark Chocolate due to undeclared milk. The product is distributed in five states.
Lima is recalling 20 Delta Cup Beater Positioner units in the US due to suboptimal welding that may reduce mechanical strength and cause breakage during use.
Harmless Harvest is recalling four varieties of probiotic drinks because testing identified Candida lusitaniae as the cause of premature spoilage.
Texas Natural Meats is recalling approximately 116 pounds of frozen beef tongue products that may be contaminated with specified risk materials (SRMs).
San Gennaro Foods is recalling Green Chili Cilantro Organic Polenta because date coding ink was printed directly on the food contact surface, allowing contact with the product.
San Gennaro Foods is recalling multiple brands of polenta because date coding ink was printed directly on the food contact surface of the packaging.
bioMérieux is recalling VITEK2 GP-ID cards because atypical negative reactions caused quality control testing failures.
Epimed International is recalling COUDE Blunt Nerve Block Needles due to a potential seal defect that may compromise sterility.
Ace Surgical Supply Co. is recalling 25 vials of Succinylcholine 20 mg/mL due to an incorrect expiration date on the outer poly bag labeling.
San Gennaro Foods is recalling pre-cooked polenta because date coding ink was printed directly on the food contact surface of the packaging.
Aaren Scientific Inc. is recalling 786 boxes of AERO IOL Injection Systems because the recommended storage temperature on the label is incorrect.
Bioseal Corporation is recalling custom surgical kits containing Aplicare Providone Iodine Prep Pads due to incorrect expiration dates.
Invivo Corporation is recalling 529 Xper Flex Cardio PhysioMonitoring systems because of intermittent communication issues between the host system and the device.
Harmless Harvest is recalling four varieties of probiotic drinks because testing identified Candida lusitaniae as the cause of premature spoilage.
San Gennaro Foods is recalling Melissa's Original Polenta because date coding ink was printed directly on the food contact surface, allowing the unapproved ink to contact the product.
Encore Medical, Lp is recalling 1,815 units of Cobalt MV with Gentamicin bone cement because the sterile Tyvek packaging seal was lost.
Boston Scientific is recalling four VIGILANT X4 CRT-D devices due to incorrect firmware configuration. The devices were distributed to medical facilities in Minnesota and Ohio.
Boston Scientific is recalling five Resonate EL ICD VR devices due to incorrect firmware configuration. The devices were distributed to medical facilities in Minnesota and Ohio.
Harmless Harvest is recalling four varieties of Probiotic drinks because testing identified Candida lusitaniae as the cause of premature spoilage.
BioMerieux SA is recalling 911 units of NucliSENS Lysis Buffer because residual heme may inhibit PCR reactions, leading to uninterpretable test results.
Boston Scientific is recalling 11 Resonate X4 CRT-D devices due to incorrect firmware configuration. The devices were distributed to medical facilities in Minnesota and Ohio.
Encore Medical is recalling Biomet Cobalt HV Bone Cement because the sterile Tyvek packaging seal may be lost, potentially compromising sterility.
San Gennaro Foods is recalling multiple brands of organic polenta because date coding ink was printed directly on the food contact surface of the packaging.
Becton Dickinson is recalling 90,000 blood collection tubes due to incorrect labeling at the case and shelf pack level.
Northgate Technologies is recalling 186 electrohydraulic lithotripter probes due to incorrect reference numbers on labels, which could delay patient care.
San Gennaro Foods is recalling Ancient Harvest and Anna's Country Kitchen quinoa polenta because date coding ink was printed directly on the food contact surface of the packaging.
San Gennaro Foods is recalling Sundried Tomato Polenta because date coding ink was printed directly on the food contact surface of the packaging.
Boston Scientific is recalling four Momentum X4 CRT-D devices due to incorrect firmware configuration. The devices were distributed to medical facilities in Minnesota and Ohio.
San Gennaro Foods is recalling sundried tomato polenta products because non-food-grade ink was printed directly on the packaging, allowing it to contact the food.
Harmless Harvest is recalling four varieties of probiotic drinks because testing identified Candida lusitaniae as the cause of premature spoilage.
Veronica's Treats, Inc. is recalling Day of the Dead Truffle Cake Pops because they may be contaminated with mold. The product was distributed in several states.
San Gennaro Foods is recalling Frieda's Variety Pack pasta sauces because date coding ink was printed on the food contact surface of the packaging.
Blue Line Food Service Distribution is voluntarily recalling specific batches of Deep Dish pre-mix dough because pieces of plastic pen were found in the product.
San Gennaro Foods is recalling White Polenta because date coding ink was printed directly on the food contact surface, allowing the unapproved ink to touch the product.
San Gennaro Foods is recalling Melissa's Italian Herb Polenta because date coding ink was printed directly on the food contact surface, allowing the unapproved ink to touch the product.
San Gennaro Foods is recalling Basil Garlic Polenta because date coding ink was printed directly on the food contact surface, allowing the unapproved ink to contact the product.
San Gennaro Foods is recalling Frieda's Mushroom and Onion Organic Polenta because date coding ink was printed directly on the food contact surface. The ink is not approved for food use.
San Gennaro Foods is recalling Melissa's Sun-Dried Tomato Polenta because date coding ink was printed on the food contact surface, allowing unapproved ink to contact the product.
Dr. Reddy's is recalling Doan's Pain Relieving Cream because the lot number on the outer packaging does not match the bottle. This is a Class III labeling recall.
Sukhi's Gourmet Indian Foods is recalling frozen chicken tikka masala products due to possible Listeria monocytogenes contamination. No illnesses have been reported.
Four Star Imports is recalling Go Wheels self-balancing scooters sold at Village Mart because the lithium-ion batteries can overheat, posing fire and explosion risks.
Dollar Mania is recalling Sonic Smart Wheels hoverboards because their lithium-ion batteries can overheat, posing fire and explosion risks.
Mercedes-Benz is recalling 72 vehicles from 2017 models due to a power steering control unit defect that may disable assist, increasing crash risk.
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