Archive
1,035 recalls were announced in October 2016.
Of the 1,035 recalls this month scored against our rubric, 13% are Critical, 29% are Severe.
Which agencies issued them
Mazda is recalling 2004-2008 RX-8 vehicles because fuel pump sealing rings may deteriorate and leak fuel, increasing the risk of a fire.
Mitsubishi is recalling 2011-2015 Outlander Sport vehicles because water leaks can corrode the wiper motor, potentially causing loss of visibility and increasing crash risk.
Mitsubishi is recalling 2007-2013 Outlander vehicles because water intrusion can corrode the wiper link, potentially causing the wipers to stop working and reducing visibility.
Mazda is recalling 2010-2011 Tribute vehicles because a cracked fuel delivery module may leak fuel, increasing the risk of fire.
Jaguar is recalling 2017 F-Type SVR vehicles because rear suspension bolts may fail prematurely, potentially causing loss of vehicle control.
Vega Helmet Corporation is recalling specific XTA and XTA Touring half helmets because they may not adequately protect the wearer's head in a crash.
Forest River is recalling 92 model year 2017 Salem and Wildwood recreational trailers because the Federal Placard Label and VIN incorrectly state the vehicles have two axles instead of one.
Starcraft RV is recalling 94 model year 2017 AR-ONE trailers because incorrect Federal Placard and Cargo Carrying Capacity labels may lead to overloading and increased crash risk.
Con-Tech is recalling 2015-2017 BridgeKing concrete mixer trucks because fender mounts may crack, causing fenders to detach and create road hazards.
REV Recreation Group is recalling 2015-2016 Holiday Rambler Vacationer motorhomes because a front truss may not be adequately supported, risking wire or hydraulic line damage.
Peg Perego is recalling about 3,000 850 Polaris Sportsman ride-on vehicles because a circuit board defect can cause overheating, fire, and burns.
Forest River is recalling 2017 Vibe trailers because the kitchen stove may be connected to a live electrical circuit, posing a shock hazard.
Jayco is recalling 2017 Jay Sport camping trailers because tire labels list the wrong tire size and pressure, which could lead to over-inflation and tire failure.
Fresh From Texas Inc. is recalling 2,121 units of Fruit & Veg Combo Trays in Texas due to potential Listeria monocytogenes contamination.
K & P Marketplace Ltd. is recalling sliced smoked Atlantic salmon after FDA environmental samples detected Listeria monocytogenes.
K & P Marketplace Ltd. is recalling Atlantic Smoked Salmon after FDA environmental samples detected Listeria monocytogenes. The product was distributed in Connecticut and New York.
SOS Telecom Inc. is recalling Super Samurai-X dietary supplements because FDA testing found undeclared sildenafil and/or its analogs.
Gaiser's European Style Provision Inc. is recalling approximately 3,895 pounds of chicken and pork bologna products due to misbranding, undeclared milk allergens, and uninspected meat.
QualiTech is recalling FE Bacon (Lot 31750) because a supplier reported the potential presence of E. coli O121 bacteria.
QualiTech, Inc. is recalling FE Spinach 352 due to a supplier notification regarding the potential presence of E. coli O121 bacteria.
Fresh From Texas Inc. is recalling specific HEB Ready Fresh Go sliced red apple products in Texas due to potential Listeria monocytogenes contamination.
New Seasons Market is recalling Creamy Almond Butter because some jars labeled as almond butter actually contain peanut butter. This labeling error poses a risk to consumers with peanut allergies.
Louis Hong Inc Dba Mei Shun Noodle Inc is recalling 6 Five Rice Noodles due to undeclared shrimp, soybean oil, and green onions.
Fresh From Texas Inc. is recalling HEB Ready Fresh Go Carrots, Apples & Celery with Ranch Dip due to potential Listeria monocytogenes contamination.
SOS Telecom Inc. is recalling Ninja-X dietary supplements because FDA analysis found undeclared sildenafil or its analogs. The product was marketed without an approved NDA or ANDA.
SOS Telecom Inc. is recalling Tiger-X dietary supplements because FDA testing found undeclared sildenafil or analogs. The product was marketed without an approved NDA or ANDA.
Good Earth Egg Company is recalling shell eggs that may be contaminated with Salmonella. The product was distributed to customers in Georgia, Illinois, Kansas, and Missouri.
SOS Telecom Inc. is recalling Ginseng Power-X capsules because FDA testing found undeclared sildenafil or analogs.
Fresh From Texas Inc. is recalling 45 oz. Fruit Party Trays due to potential Listeria monocytogenes contamination. The product was distributed in Texas.
Leonhard Lang is recalling Skintact DF29N defibrillation electrodes because they may not connect to Welch Allyn AED 10 devices promptly, delaying life-saving treatment.
SenTec AG is recalling 75 SDMS units because a loose screw may cause short circuits, leading to fire or electrical shock.
Kabobs Inc is recalling Mini Classic French Quiche because it was manufactured with flour contaminated with E. coli O121.
QualiTech is recalling FE Maple product code 27128 due to potential E. coli O121 bacteria. The product was distributed in ten US states and Canada.
Ford is recalling 2015-2017 Mustangs because an engine oil cooler hose may separate, causing an oil leak that could lead to engine failure or fire.
QualiTech is recalling FE Carrot 281 because a supplier notified them of potential E. coli O121 bacteria in the material.
Synergetics Inc is recalling 72 units of 25 gauge VersaVit 2.0 Core Essentials Procedure Packs because the vitrectomy cutters do not operate within correct pressure pulse specifications.
QualiTech is recalling 3,200 lbs of FE Jalapeno 709 due to potential E. coli O121 contamination. The product was distributed in 10 US states and Canada.
Dollar General is recalling Soft Baked Chocolate Brownie Cookies due to the presence of mold. Consumers should discard the product or return it for a refund.
Fresh From Texas Inc. is recalling HEB Ready Fresh Go Fresh Fruit Medley 7 oz. packages due to potential Listeria monocytogenes contamination.
QualiTech is recalling FE Jalapeno 321A because a supplier reported the potential presence of E. coli O121 bacteria.
Windstone Medical Packaging is recalling 852 Major General Packs because Medtronic gloves inside may have splits or holes that compromise sterility.
Union Bagel Shop is recalling sourdough bagels because they contain undeclared wheat. The products were sold at one retail store in Grande, Oregon.
Windstone Medical Packaging is recalling 115 Peri Kits (PSS1037) because the included Medtronic gloves may contain splits or holes that compromise sterility.
Vascular Solutions is recalling Twin-Pass RX Dual Access Catheters because excess manufacturing material may remain at the tip or within the distal lumen.
Fresh From Texas Inc. is recalling HEB Ready Fresh Go Sliced Red Apples With Caramel Dip due to potential Listeria monocytogenes contamination.
QualiTech is recalling 40,080 lbs of dry blueberry and strawberry blend due to potential E. coli O121 contamination.
Forest River is recalling 2016 Rockport cargo and work trucks because the rear ramp may damage fuel connections, causing engine stalls and crash risk.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because splits or holes may compromise sterility in custom surgical kits.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because they may contain splits or holes that compromise sterility.
Vascular Solutions is recalling Twin-Pass dual access catheters because excess manufacturing material may remain at the tip or in the distal lumen.
Food Gusto, Inc. is recalling Birdy 3 in 1 Robusta Coffee Mix because it may contain undeclared milk and has unclear nutritional labeling.
Arbor Pharmaceuticals is recalling Cetylev (acetylcysteine) effervescent tablets because incomplete seals on the blister packaging allow moisture to enter, causing the tablets to swell.
Ford is recalling specific 2010-2012 Escape and 2010-2011 Mariner vehicles because a cracked fuel delivery module may cause a fuel leak, increasing the risk of fire.
Del Monte is recalling cut green beans and field peas with snaps due to a customer complaint of finding crawfish parts in the product.
QualiTech is recalling 176,900 lbs of PE Blueberries due to potential E. coli O121 contamination. The product was distributed to multiple US states and Canada.
Heartware, Inc. is recalling Ventricular Assist System Controllers due to loose connector ports. The recall affects 4,235 units worldwide, including 7,272 in the U.S.
Del Monte is recalling approximately 15,000 cases of canned field peas and green beans after a customer complaint reported finding crawfish parts in the product.
Vascular Solutions is recalling Twin-Pass dual access catheters because excess manufacturing material may remain at the catheter tip or within the distal rapid exchange lumen.
Ford is recalling 2017 F-250 through F-550 Super Duty trucks because a fuel shield may detach, causing a leak that increases fire risk.
Fresh From Texas Inc. is recalling 18,392 units of Deluxe Fruit Tray 52 oz. due to potential Listeria monocytogenes contamination.
Dream Body Weight Loss is recalling Dream Body Extreme Gold capsules because they contain undeclared sibutramine and were marketed without FDA approval.
Teleflex Medical is recalling Willy Rusch Tracheostomy Tube Sets because the connector may disconnect from the tube during use.
QualiTech, Inc. is recalling 1,400 lbs of FE Rainbow Blend because a supplier notified the company of potential E. coli O121 bacteria in the material.
Windstone Medical Packaging is recalling 304 Endoscopy Packs because disposable gloves in the kits may have splits or holes that compromise sterility.
Dream Body Weight Loss is recalling Dream Body 450 mg capsules because they contain undeclared sibutramine and were marketed without FDA approval.
RTI Surgical is voluntarily recalling 66 units of Streamline OCT spinal rods due to potential cracks that could reduce strength and cause patient injury.
QualiTech is recalling 400 lbs of FE Bacon 286 because a supplier reported the potential presence of E. coli O121 bacteria.
Fresh From Texas Inc. is recalling HEB Ready Fresh Go Carrots and Apples due to potential Listeria monocytogenes contamination.
Awareness Corporation is recalling 2,697 bottles of Boost Tea dietary supplement due to potential Salmonella contamination. The product was distributed in 34 U.S. states and D.C.
Fresh From Texas Inc. is recalling 34,425 units of packaged apples in Texas due to potential Listeria monocytogenes contamination.
Fresh From Texas Inc. is recalling HEB Ready Fresh Go Carrots, Apples with Sesame Sticks & Hummus due to potential Listeria monocytogenes contamination.
Windstone Medical Packaging is recalling 816 Extremity Tray kits because the included Medtronic gloves may have splits or holes that compromise sterility.
X Spine Systems is recalling 1,186 Calix T PEEK Lumbar System trial devices because components may detach and lodge in the intervertebral space during surgery.
QualiTech is recalling 4,150 lbs of red bell peppers due to potential E. coli O121 contamination. The product was distributed in ten US states and Canada.
QualiTech, Inc. is recalling 300 lbs of green bell peppers due to potential E. coli O121 contamination. The product was distributed to multiple US states and Canada.
Windstone Medical Packaging is recalling 12 Major Laparotomy Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.
Dream Body Advanced 400 mg capsules are being recalled because they contain undeclared sibutramine and were marketed without an approved NDA/ANDA.
X Spine Systems is recalling 195 units of Calix T PEEK Lumbar System TLIF Rasps because the tools may detach and become lodged in the surgical site.
QualiTech is recalling frozen red bell peppers due to a potential presence of E. coli O121 bacteria reported by a supplier.
Fresh From Texas Inc. is recalling HEB Ready Fresh Go fruit cups due to potential Listeria monocytogenes contamination. The product was distributed in Texas.
QualiTech is recalling FE Cheddar Cheese because a supplier reported the potential presence of E. coli O121 bacteria.
Fresh Express is recalling American Salad bags that may contain incorrect condiment kits. Consumers in six states should check their products.
Windstone Medical Packaging is recalling 204 plastic packs used in general surgery because the included Medtronic gloves may contain splits or holes that compromise sterility.
Fresh From Texas Inc. is recalling 10-ounce packages of Apples & Grapes sold in Texas due to potential Listeria monocytogenes contamination.
Union Bagel Shop is recalling Cowboy Cookies In-a-Jar because the packaging fails to declare wheat, milk, and soy allergens.
QualiTech, Inc. is recalling specific lots of green bell peppers due to a potential presence of E. coli O121 bacteria identified by a supplier.
QualiTech, Inc. is recalling 500 lbs of FE Bacon because a supplier notified them of potential E. coli O121 bacteria in the material.
QualiTech is recalling FE Rainbow Blend 714 because a supplier notified them of potential E. coli O121 bacteria contamination.
QualiTech is recalling 6,000 lbs of red bell peppers due to potential E. coli O121 contamination. The product was distributed to 10 US states and Canada.
Kabobs Inc is recalling 377 cases of Mini Cheese Quiche because the flour used was contaminated with E. coli O121. The product was distributed across 28 states.
Windstone Medical Packaging is recalling 145 Ortho Kits because the disposable gloves included may contain splits or holes that compromise sterility.
Fred Meyer is recalling Boar's Head To Go Superfood Wraps sold in deli departments due to undeclared milk, soybeans, wheat, and cashews.
Kabobs Inc is recalling Four Cheese Puff products because they were manufactured with flour contaminated with E. coli O121.
Windstone Medical Packaging is recalling 224 Dr. Fritsch surgical kits because the included Medtronic gloves may have splits or holes that compromise sterility.
Windstone Medical Packaging is recalling 6,381 Basic Pack surgery kits because Medtronic gloves inside may have splits or holes that compromise sterility.
Ethicon Endo-Surgery Inc is recalling 213 Endoscopic Articulating Linear Cutters because a pinion gear failure could interrupt the firing stroke and expose healthcare professionals to sharps injuries.
Windstone Medical Packaging is recalling 85 Foot Pack kits because the included Medtronic gloves may contain splits or holes that compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because splits or holes may compromise sterility.
Windstone Medical Packaging is recalling Student Pack-NS surgical kits because the Medtronic gloves included may have splits or holes that compromise sterility.
Windstone Medical Packaging is recalling 1,596 General Pack I surgery kits because the included Medtronic gloves may contain splits or holes that compromise sterility.
Looking for a different month? Back to 2016.