Archive
745 recalls were announced in November 2015.
Of the 745 recalls this month scored against our rubric, 3% are Critical, 53% are Severe.
Which agencies issued them
Kar Nut Products is recalling Southern Grove On The Go Trail Mix because the product may contain very small pieces of glass.
Maplehurst Bakeries is recalling German Chocolate Layer Cakes sold at Publix in Florida and Georgia because the labels listed ingredients for a different product.
National Frozen Foods Corporation is recalling frozen Italian Vegetable Blend due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Kronos Foods is recalling Baklava Assortment due to potential metal fragments discovered after increased metal detector rejections.
S. Martinelli & Co is recalling Martinelli's Gold Medal Sparkling Cider due to the potential for glass fragments in the bottles.
National Frozen Foods Corporation is recalling Sysco Classic and Imperial Italian Vegetable Blend due to potential Listeria monocytogenes contamination.
Certified Smoked Fish LLC is recalling 13 units of Cold Smoked Salmon Trim in California due to potential Listeria monocytogenes contamination.
Kronos Foods is recalling Classic Baklava because metal fragments were detected during quality control. Consumers should stop eating the product and return it to the store.
National Frozen Foods Corporation is recalling frozen Italian Vegetable Blend due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
National Frozen Foods is recalling frozen Italian Vegetable Blend due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
NatureBox is recalling Sticks 'n Stones trail mix because the oil used to roast nuts was also used for peanuts, which are not listed on the label.
Prova Inc is recalling 750 lbs of vanilla seeds due to the potential for small pieces of metal. The product was distributed to one customer in Wisconsin.
Northstar Produce is recalling 98 cases of Granny Smith apples because testing indicated the presence of Listeria, Salmonella, and/or E. coli.
Kar Nut Products Company is recalling 16,744 boxes of Kar's 18 CT. Variety Pack nuts due to the possibility of very small pieces of glass in the product.
Kar Nut Products Company is recalling Kar's Sweet n' Salty Mix due to the possibility that the product may contain very small pieces of glass.
Kar Nut Products Company is recalling Kar's Sweet n' Salty Mix because the product may contain very small pieces of glass.
Roche Diagnostics is recalling Bulk Loader Modules for cobas p 512/612 instruments because sample tubes may open during transport, causing system and sample contamination.
Civco Medical Instruments is recalling 717 boxes of Infiniti Plus Needle Guides because the sterility of the product cannot be assured.
Ameditech is recalling EDI BZO Uncut Sheet-Card drug abuse tests because they have shown reduced reactivity. The affected units were distributed nationwide in the US and internationally to Australia.
Civco Medical Instruments is recalling PercuNav tracking bracket kits because the sterility of the product cannot be assured.
Certified Smoked Fish LLC is recalling Cold Smoked Salmon Deli trays in California due to potential Listeria monocytogenes contamination.
Newmar is recalling 2016 King Aire vehicles that may lack a required emergency exit window over the driver's side dinette table, potentially delaying escape during an emergency.
National Frozen Foods Corporation is recalling frozen Italian green beans due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Ameditech is recalling Micro Screen 6 Panel Cup drug abuse tests because they have shown reduced reactivity.
Cyberonics is recalling 27 Model 106 Vagus Nerve Stimulator generators due to delays in heartbeat detection and potential decreased battery longevity.
Kanan Enterprises is recalling Mountain Mix trail mix products because they contain undeclared milk. The products were distributed to 21 states and Canada.
Civco Medical Instruments is recalling 508 boxes of Needle Guide Starter Kits because the sterility of the product cannot be assured.
Ameditech is recalling DrugCheck Waived 12 Panel Cup tests because they have shown reduced reactivity.
Civco Medical Instruments is recalling 54 boxes of Large Gauge Infiniti Plus Needle Guides because the sterility of the product cannot be assured.
Synthes is recalling 267 previously repaired Sternal ZIPFIX Application Instruments because the screws may break or loosen.
Forest River is recalling specific 2007-2015 motorhomes because a bolt on the electric entry steps may fracture, causing the steps to become unstable and increasing the risk of injury.
Stryker Howmedica Osteonics Corp. is recalling six PCA 10 Degree Hooded Acetabular Inserts because the 22 mm size was inadvertently omitted from the FDA 510(k) clearance.
Civco Medical Instruments is recalling 1,139 boxes of Biopsy Starter Kits because the sterility of the product cannot be assured.
Downing Labs, LLC is recalling 106 vials of Hydroxocobalamin Injection due to a lack of assurance of sterility. The product was distributed nationwide and internationally.
Del Monte is recalling 270 units of Fresco Fresh Strawberry Yogurt Parfait in North Carolina, South Carolina, and Virginia due to potential undeclared almonds.
Leonhard Lang Medizintechnik GmbH is recalling specific lots of ECG electrodes because they may fail to transmit signals or transmit poor signals before expiration.
Columbia Northwest is recalling 2013-2014 Somerset E1 and Santa Fe trailers because the water heater may overheat, causing scalding.
Downing Labs, LLC is recalling Taurine Injectable, 50mg/mL, 30mL vials due to a lack of assurance of sterility. The recall affects 123 vials distributed nationwide and internationally.
Kronos Foods is recalling Orange Blossom Baklava due to the potential for metal fragments in the baked goods.
US Compounding Inc is recalling 1,421 vials of Lincomycin/Lidocaine due to deficient practices that may impact sterility assurance.
Brainlab AG is recalling 12 Image Guided Surgery systems in the US and Australia because data sets were not accurately registered to patient anatomy.
Philips is recalling ECG sync cables used with HeartStart monitors because electrical interference can cause misinterpretation of heart signals or interrupt pacing.
Precision Medical is recalling 315 Easy Dial Oxygen Regulators because the settings label may be off by one position, causing incorrect oxygen flow.
Ameditech is recalling 11 Panel Dip Cards (OPI 2000 and OPI 300) because they have shown reduced reactivity. The recall covers 150 units distributed in the US and Australia.
Par Pharmaceutical is recalling Meclizine Hydrochloride Tablets because they failed impurity specifications. The recall covers 100 and 1000-count bottles distributed nationwide.
Enjoy Life Natural Brands is recalling Semi-Sweet Chocolate mini chips because they may contain undeclared sunflower seeds, pumpkin seeds, and dried fruit.
Ameditech is recalling 11 Panel Drug Abuse Tests because they have shown reduced reactivity. The affected products are distributed in the US and Australia.
Mylan Institutional is recalling 4,609 packages of Meclizine Hydrochloride 25 mg tablets because they failed impurity specifications.
Ameditech is recalling DrugSmart 10 Test Cups because they have shown reduced reactivity. The affected units were distributed nationwide in the US and internationally to Australia.
Vintage Pharmaceuticals is recalling 912 bottles of 12.5 mg Hydrochlorothiazide capsules because of the presence of particulate matter.
Ameditech is recalling 7,482 units of CLIA RDTC 12-Panel Cup drug abuse tests because they have shown reduced reactivity. The products were distributed in the US and Australia.
Ameditech is recalling ArcPoint Labs 10 Panel Dip Screen (OXY) drug tests because they have shown reduced reactivity.
New Frontier Foods is recalling Ocean's Halo Korean BBQ Seaweed Chips because routine tests found gluten levels above the FDA limit for gluten-free products.
New Frontier Foods is recalling Ocean's Halo Chili Lime Seaweed Chips because routine tests found gluten levels above the FDA limit for gluten-free products.
Herr's Foods is recalling Sour Cream & Onion Potato Chips because packaging incorrectly states the product is gluten-free, despite containing wheat.
Astora is recalling 52 units of the MiniArc Pro Single incision Sling System because the lot number on the outer carton did not match the labels inside the box.
TZ Medical Inc. is recalling Neptune Plus hemostasis pads because the instructions for use do not match the original FDA submission.
Ameditech is recalling ProScreen drug panel tests because they have shown reduced reactivity. The recall covers 31,530 units distributed in the US and Australia.
Ameditech is recalling iCup drug screen cups because they have shown reduced reactivity. The affected units were distributed nationwide in the US and internationally to Australia.
Ameditech is recalling Premier Clia Waived 12 Panel Tilt Cup drug tests because they have shown reduced reactivity.
TZ Medical Inc. is recalling 10,180 units of SilverStat hemostasis pads because the instructions for use did not match the original FDA submission.
Ameditech is recalling 12-Panel Dip Drug Screens with adulterant because they have shown reduced reactivity. The affected units were distributed nationwide in the US and internationally to Australia.
Ameditech is recalling 70 units of DrugCheck Pipette 10 Drug Tests because they have shown reduced reactivity. The affected tests were distributed in the US and Australia.
Agfa Healthcare is recalling IMPAX CV software versions 7.8.x and 12.x because the Demographics Manager feature may generate incorrect PDF reports after physician signature.
Ameditech is recalling 787 kits of 1 Step 12 Panel Cup drug tests due to reduced reactivity. The products were distributed in the US and Australia.
Ameditech is recalling 2,240 units of 6 Panel Cup Body and Lid drug tests because they have shown reduced reactivity.
Ameditech is recalling specific Immutest drug screen cups because they have shown reduced reactivity. The affected units were distributed nationwide in the US and in Australia.
Ameditech is recalling Thermo Fisher 6 Drug Cassettes because they have shown reduced reactivity. The recall affects 220 units distributed in the US and Australia.
Ameditech is recalling specific DrugSmart drug abuse test cups because they have shown reduced reactivity. The affected units were distributed in the US and Australia.
Ameditech is recalling 160 units of DrugSmart Dip drug abuse tests because they have shown reduced reactivity. The affected products were distributed in the US and Australia.
Ameditech is recalling 10-Panel Pipette Drug Screen tests because they have shown reduced reactivity. The recall affects 200 units distributed in the US and Australia.
Ethicon Endo-Surgery is recalling Harmonic ACE+ 7 Laparoscopic Shears because holes in the Tyvek packaging can compromise the sterile barrier.
Medacta USA is recalling 4 units of GMK Hinge knee prostheses because they contain 5 mm screws instead of the required 10 mm screws.
Par Pharmaceutical is recalling specific lots of Meclizine Hydrochloride 12.5 mg tablets because they failed impurity specifications.
Akorn, Inc. is recalling 6,861 vials of RIFAMPIN FOR INJECTION USP, 600 mg because a known impurity failed to meet specifications.
Akorn, Inc. is recalling 13,896 bottles of Hydrocortisone and Acetic Acid Otic Solution because the bottles are missing the safety seal around the neck.
Baxter is recalling HomeChoice and HomeChoice Pro APD systems due to loud operating sounds. The devices function correctly, but the noise is unacceptable to users.
SalesOne is recalling light-up ear plug jewelry sold at Spencer Gifts because battery acid can leak and cause burns. Consumers should stop wearing the product and contact SalesOne for a refund or replacement.
Mercedes-Benz is recalling 809 model year 2014 E350 sedans because a fuel feed line defect may cause a leak or disconnection, increasing the risk of fire or a crash.
Ford is recalling 2016 F-650 trucks built between July 29 and September 3, 2015, because an incorrect steering column may cause the park pawl to fracture, allowing the vehicle to move unexpectedly.
VT Hackney is recalling certain 2015 Kidron Refrigerated Trailers because improperly tightened caliper bolts may allow the brake caliper to detach, reducing braking performance.
Wabash is recalling 2013-2015 Van Trailers because brake caliper bolts may not be tightened, risking caliper detachment and reduced braking.
Ford is recalling 2010-2011 Fusion and Mercury Milan vehicles because fuel vapor canister purge valves may fail, causing fuel tank cracks and leaks that increase fire risk.
Mercedes-Benz is recalling 2015 S550E Hybrid vehicles because a defective onboard charger may cause the car to unexpectedly shift to park, increasing crash risk.
Subaru is recalling 2016 Legacy and Outback vehicles because improperly tightened nuts may allow the drive shaft to separate, potentially causing a fuel leak and fire.
MVP Group is recalling about 720,000 glass jar candles with lids because the glass lids can break when opened, posing a laceration hazard.
Nissan is recalling 2015-2016 GT-R vehicles sold in Puerto Rico because the certification label is missing weight rating information, which could lead to vehicle overloading.
Exmark is recalling about 500 2015 Quest riding mowers because brittle fuel filters can leak fuel, posing a fire hazard. No injuries have been reported.
Mars Symbioscience is recalling about 5,000 CocoaVia brand frothers because the spring can detach, posing a choking hazard. No injuries have been reported.
Toro is recalling about 8,600 2015 TimeCutter riding mowers because fuel filters can fracture and leak, posing a fire hazard. No injuries have been reported.
BRP is recalling about 2,800 2016 Ski-Doo snowmobiles because internal fuel hose damage can cause leaks and fire. No injuries have been reported.
Lutron Electronics is recalling about 240 custom-made Roman shades sold in the U.S. because exposed tape creates a strangulation risk for children.
Strick Trailers is recalling 1998-2005 Dry Freight Van Trailers because rear impact guards may fail to prevent vehicles from sliding underneath during a crash.
BMW is recalling 2015-2016 M3 and M4 vehicles because a driveshaft slip-joint may lack grease, potentially causing loss of power and increasing crash risk.
Tesla is recalling 2012-2015 Model S vehicles because front seat belts may be improperly connected to the pretensioner, increasing injury risk in a crash.
Supreme is recalling 2015-2016 Classic American Trolley vehicles because their windshields do not meet federal safety standards, potentially reducing driver visibility.
Crossroads RV is recalling 2016 ReZerve travel trailers because the Federal Identification Label incorrectly states the axle capacity, potentially leading to overloading and loss of control.
Suzuki is recalling 600 model year 2016 GSX-S1000, GSX-S1000A, and GSX-S1000FA motorcycles because front brake calipers may leak fluid, reducing braking performance.
BMW is recalling 2015-2016 Rolls-Royce Phantom vehicles because side curtain air bags may not deploy correctly, increasing injury risk in crashes.
Navistar is recalling 2013-2014 International trucks because a faulty accelerator pedal sensor can cause high engine idle, increasing crash risk on downgrades.
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