Archive
913 recalls were announced in January 2017.
Of the 913 recalls this month scored against our rubric, 11% are Critical, 52% are Severe.
Which agencies issued them
Chesapeake Spice Company is recalling Enchilada Seasoning because a milk ingredient used in the product was recalled.
Chesapeake Spice Company is recalling 9,650 units of Green Bean Sauce Seasoning because a recalled milk ingredient was used in the product.
Baxter Healthcare is recalling 8,640 APD Set with Cassette 3-Prong Peritoneal Dialysis Sets due to customer complaints about leaks.
Meridian Bioscience is recalling Premier EHEC and Premier EHEC Bulk diagnostic kits because internal testing showed they can produce false positive results with some broth specimens.
Dieffenbach's Potato Chips, Inc. is voluntarily recalling Sour Cream and Onion Kettle Chips because the seasoning may contain traces of Salmonella.
Hungry Heart Bakery is recalling Cracker Jax because the product contains milk and soy that are not declared on the label.
UCI-FRAM is recalling FRAM Model G2 inline fuel filters because oversized connection hoses may cause fuel leaks, increasing fire risk.
Ultradent Products, Inc. is recalling NanoTips 30g dental tips because the stainless steel cannula may detach from the base, posing a risk during intra-oral procedures.
Great Northern Bakehouse is recalling Birdman Bread sold in Montana because it contains undeclared soy lecithin from a pan spray.
Fresenius Medical Care is recalling 2008K2 hemodialysis systems because a software error may cause the machine to execute a cancelled ultrafiltration rate instead of the displayed rate.
O'Pelle Enterprises is recalling frozen raw Egg Bagels because the label fails to declare Yellow 5. The product was distributed only within Florida.
Shire PLC is recalling 4,520 bottles of Pentasa (mesalamine) 250 mg capsules because 500 mg capsules were found in the bottles.
Exactech, Inc. is recalling 12 polyethylene acetabular liners because they were labeled with incorrect Global Trade Item Numbers (GTINs).
Zimmer Biomet is recalling 19 ArComXL Polyethylene Bearings because packaging labels did not match the physical product inside, posing a risk of surgical delay.
Town and Country Compounding is recalling 101 vials of HCG because potency testing showed 74%, below the required 80-125% range.
O'Pelle Enterprises is recalling frozen raw Egg Bagels because the label fails to declare Yellow 5, a common food dye.
Sandoz Inc. is recalling specific lots of Donepezil Hydrochloride 10 mg tablets because they failed potency tests. The medication may not contain the full prescribed dose.
Exactech is recalling 98 Alteon Neck Preserving Stems because they were labeled with incorrect Global Trade Item Numbers (GTINs) that identify them as different devices.
Medacta USA Inc. is recalling 82 M.U.S.T. Rods due to damaged packaging and lack of sterility assurance. The recall covers units distributed in the US and several international countries.
Endologix is updating the Instructions for Use and implementing modifications to the AFX Endovascular AAA System.
Endologix updated the Instructions for Use for the AFX Endovascular AAA System to address endoleak Type IIIB.
The Binding Site Group is recalling Digital RID Plate Readers and software because a defect may prevent the system from flagging out-of-range quality control results.
The Binding Site Group is recalling 1,002 units of the Freelite Human Lambda Free SPAPlus Kit because calibration curve activity increased over time.
Endologix is recalling the AFX2 Endovascular AAA System to provide updated information regarding Type III endoleak rates and patient surveillance.
Beckman Coulter is recalling four AutoMate 2500 Family units in Maryland to update the PC image for Windows 10 compatibility.
L. Perrigo Company is recalling 162,534 tubes of Clindamycin Phosphate and Benzoyl Peroxide Gel because a small number of tubes may contain mold on the cap.
Zimmer Biomet is recalling 36 units of ArComXL polyethylene liners because packaging labels did not match the physical product, posing a risk of surgical delay.
Safeway is recalling Signature Kitchens Tuna Chunk Light in 20 oz, 12 oz, and 5 oz sizes due to failed sensory analysis and decomposition.
Carestream Health Inc. is recalling Touch Prime and Touch Prime XE ultrasound systems due to a software error that may display incorrect measurement units.
Endologix updated the Instructions for Use and modified the AFX Endovascular AAA System. The correction applies to procedures conducted after July 2015.
Endologix is updating the Instructions for Use and making modifications to the AFX Endovascular AAA System. This applies to procedures conducted after October 2015.
The Binding Site Group is recalling 809 Optilite Freelite Lambda Free Kits because specific lots produce test results that are approximately 33% lower than expected.
Safeway is recalling 177 cases of Signature Kitchens Tuna Solid White 12 oz. cans because they failed sensory analysis and showed signs of decomposition.
Endologix is recalling 17,139 units of the AFX Endovascular AAA System to update the Instructions for Use and implement device modifications.
Endologix is recalling 34 units of the AFX Endovascular AAA System to provide updated information regarding Type III endoleak rates and patient surveillance.
Endologix is correcting cumulative clinical data reports for the AFX Endovascular AAA System and Powerlink System. This action applies to procedures conducted after June 2013.
O'Pelle Enterprises is recalling Rainbow Bagels because the labels fail to declare specific artificial food dyes.
DICOM GRID Inc. is recalling Ambra PACS software version V3.16.13.0 because a defect causes diagnostic images to appear washed out, potentially affecting image analysis.
Starkey Water is recalling 300 cases of 16.9 oz glass bottles of Starkey Spring Water because 12 ppb of arsenic was detected in a water sample.
Smith & Nephew is recalling RENASYS GO Negative Pressure Wound Therapy devices because they lack 510(k) clearance for a design modification.
Smith & Nephew is recalling RENASYS GO Negative Pressure Wound Therapy External Power Supply Units because they lack 510(k) clearance for a design modification.
Novum Pharma is recalling Novacort Gel sample packets because the pramoxine hydrochloride content was found to be out of specification.
Exactech is recalling 79 Novation Cemented Plus Femoral Stems because they were labeled with incorrect Global Trade Item Numbers (GTINs).
Teva Pharmaceuticals is recalling 6,800 cartons of Risedronate Sodium Delayed-release Tablets, 35 mg, because they failed dissolution specifications.
Atlas Meat Company is recalling pork sausage products because they may contain monosodium glutamate (MSG), which is not declared on the label.
Ford is recalling 2016 Focus and C-Max vehicles because improperly welded floor pan joints may reduce structural integrity, increasing injury risk in a crash.
HP is expanding a recall of about 101,000 lithium-ion batteries for HP and Compaq notebook computers because they can overheat, posing fire and burn risks.
Toyota is recalling 2016-2017 Tundra trucks with resin rear bumpers because the brackets may break if stepped on, posing an injury risk.
Ford is recalling 2017 F-150 trucks because the instrument cluster may lose power in cold weather, potentially hiding the transmission gear position and increasing crash risk.
Pulse Performance is recalling about 8,900 children's electric scooters sold at Target because a wheel component can break, posing a fall hazard to riders.
Autocar is recalling 38 Xpeditor trucks from 2013-2016 because over-braking can cause S-cam tube bolts to loosen, leading to unexpected brake engagement and increased crash risk.
IH Parts America Inc. is recalling specific steering tie rod adjusters for International Scout vehicles because they may fracture, affecting steering capability and increasing crash risk.
Autocar is recalling 2016-2017 Xspotter vehicles because they lack a dimmer switch for dash illumination, which may increase crash risk.
BMW is recalling specific 2000-2003 3, 5, and X5 series vehicles because replacement driver-side air bag inflators may rupture during deployment, posing a risk of serious injury or death.
Walker is recalling 2014-2017 Food Grade Tank Trailers because weld joints on the underride guard may crack, potentially causing the guard to detach and become a road hazard.
Maserati is recalling 39,381 vehicles due to a front seat wiring harness defect that may cause an electrical short and increase the risk of a fire.
Hans Kissle Company is recalling approximately 6,348 pounds of ready-to-eat chicken bowls due to a potential process defect that could allow bacterial pathogens to survive.
Continental is recalling specific General Tire Grabber light truck tires due to a defect that may cause tread separation, increasing the risk of a crash.
The New Haven Companies is recalling Safe Haven Wheelchair Securement Tiedowns because they may not adequately secure a wheelchair in a crash, increasing injury risk.
Airstream is recalling 2017 Sport, International, and Flying Cloud trailers because incorrect tire labels could lead to overinflation and tire blowouts.
Mountain View Packaging is recalling 1,080 pounds of sweet chili chicken products because they contain undeclared wheat, egg, and milk allergens.
Pratt Industries is recalling 126 units of 2014 DC432LS9 and DC432LS9HL ISO Tank Chassis because a defective axle spindle may cause the wheel end to separate, increasing crash risk.
Trek is recalling 720 Disc bicycles and wheel sets because broken spokes can contact the brake caliper, posing a fall hazard to riders.
Daimler Trucks North America is recalling 2016-2017 Freightliner trucks because modified instrument clusters may become unresponsive, increasing crash risk.
All American Seasonings, Inc. is recalling approximately 29 bags of 50 lb Nacho Snack Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.
St. Clair Foods is recalling Tropical Fruit Supreme products due to potential salmonella contamination from Valley Milk Dry Milk.
Sabra Dipping Company is recalling 8.5-ounce jars of Honey Mustard spread due to potential Listeria monocytogenes contamination.
Valley Milk Products is recalling Sweet Cream Buttermilk Powder in 50-pound bags due to potential Salmonella contamination. The product was distributed to brokers and direct accounts in nine states.
FONA International is recalling 1,450 pounds of N-C Butter Flavor product due to possible Salmonella contamination. The product was distributed in Illinois, Wisconsin, New Jersey, Texas, and Ontario, Canada.
Sabra Dipping Company is recalling specific lots of Rosemary/Sea Salt Hummus due to potential Listeria monocytogenes contamination.
St. Clair Foods is recalling Pineapple Nut Delight because it was made with milk powder potentially contaminated with Salmonella.
All American Seasonings is recalling specific lots of OC Ranch French Fry Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.
Sabra Dipping Company is recalling 10,498 cases of 10-ounce Jalapeno Hummus due to potential Listeria monocytogenes contamination. The product was distributed in the US and three foreign countries.
All American Seasonings is recalling 69 bags of Habanero Ranch Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.
FONA International is recalling 400 lbs of N-C Butter Flavor Nat WONF due to possible Salmonella contamination. The product was distributed in Illinois, Wisconsin, New Jersey, Texas, and Canada.
All American Seasonings is recalling Four Cheese Sauce Mix drums due to potential Salmonella contamination. The product was distributed nationwide and to Canada.
Sabra Dipping Company is recalling Sabra Hummus Lemon due to potential Listeria monocytogenes contamination. The product was distributed in the US and three foreign countries.
Sabra Dipping Company is recalling specific lots of 10-ounce Sabra Hummus 3 Pepper Chili due to the potential for Listeria monocytogenes contamination.
Blue Bell Creameries is recalling specific ice cream products due to potential Listeria monocytogenes contamination from cookie dough supplied by Aspen Hills, Inc.
Sabra Dipping Company is recalling various sizes of Pine Nut Hummus due to potential Listeria monocytogenes contamination. The products were distributed across the US and three foreign countries.
Sabra Dipping Company is recalling 10,094 cases of 10-ounce Sabra Hummus Olive due to potential Listeria monocytogenes contamination.
Sabra Dipping Company is recalling Sabra Hummus Bold & Spicy due to potential Listeria monocytogenes contamination. The product was distributed in the US and three foreign countries.
Sabra Dipping Company is recalling 10-ounce jars of Hummus Basil-Pesto due to potential Listeria monocytogenes contamination. The product was distributed across the US and three foreign countries.
Sabra Dipping Company is recalling 10-ounce Hummus Taco products due to potential Listeria monocytogenes contamination. The products were distributed throughout the US and three foreign countries.
Sabra Dipping Company is recalling various sizes of Garlic Hummus due to potential Listeria monocytogenes contamination. The product was distributed throughout the US and three foreign countries.
Blue Bell Creameries is recalling specific ice cream products containing cookie dough from Aspen Hills, Inc. due to the potential for Listeria monocytogenes contamination.
Lenny & Larry's is recalling Coconut Chocolate Chip cookies due to the possible presence of undeclared milk in the dark chocolate chips.
Sabra Dipping Company is recalling specific sizes of Spinach/Art Hummus because the products have the potential to be contaminated with Listeria monocytogenes.
All American Seasonings, Inc. is recalling 244 bags of FH White Cheddar 2410 powder due to potential Salmonella contamination.
Blue Bell Creameries is recalling four ice cream products containing cookie dough from Aspen Hills, Inc. due to the potential presence of Listeria monocytogenes.
All American Seasonings, Inc. is recalling 219 bags of Super Otirod seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.
Sabra Dipping Company is recalling various sizes of Sabra Hummus Classic due to potential Listeria monocytogenes contamination. The product was distributed throughout the US and three foreign countries.
FONA International is recalling 300 lbs of N-C Chai Tea Flavor due to possible Salmonella contamination. The product was distributed in Illinois, Wisconsin, New Jersey, Texas, and Canada.
Sabra Dipping Company is recalling multiple sizes of Red Pepper Hummus due to potential Listeria monocytogenes contamination. The product was distributed across the US and three foreign countries.
Blue Bell Creameries is recalling specific ice cream products due to the potential presence of Listeria monocytogenes from a supplier.
Sabra Dipping Company is recalling 10-ounce containers of Sun-Dried Tomato Hummus due to potential Listeria monocytogenes contamination.
GE Healthcare is recalling Infant Warmer Systems because loose screws in the Heater Head could fall and cause thermal injury to patients.
All American Seasonings is recalling 50 lb bags of Jalapeno Popper Snack Seasoning due to potential Salmonella contamination.
Sabra Dipping Company is recalling 10-ounce containers of Caramelized Onion Hummus due to potential Listeria monocytogenes contamination. The product was distributed in the US and three foreign countries.
United Food Ingredients, Inc. is recalling 400 lbs of Ranch Seasoning Complete due to potential Salmonella contamination. The product was distributed in Illinois and Wisconsin.
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