Archive
399 recalls were announced in June 2014.
Of the 399 recalls this month scored against our rubric, 7% are Critical, 23% are Severe.
Which agencies issued them
S&S Truck Parts is recalling Newstar brand aftermarket drag link assemblies for Kenworth and Peterbilt trucks because they were not manufactured to proper specifications, posing a risk of steering system failure.
Nova Bus is recalling 2010-2014 LFS transit buses because a fractured alternator cable terminal may cause arcing and an engine compartment fire.
Graco is recalling specific rear-facing child seats because the harness buckle may get stuck, making it difficult to remove a child in an emergency.
Nova Bus is recalling 796 LFS transit buses from model years 2004 and 2006-2013 because the ABS malfunction light may not illuminate if the control unit loses power.
General Motors is recalling specific 2014-2015 Chevrolet and GMC vehicles because an electrical short may cause the transfer case to shift to neutral unexpectedly.
Special Fleet Service is recalling 2009-2013 modified Ford F-350, F-450, and F-550 trucks because oil leaks from the PTO pressure switch may ignite the exhaust thermal blanket.
Winco Fireworks is recalling Contraband 24 kits because narrow tubes can cause shells to explode, posing burn and impact risks.
General Motors is recalling 2013-2014 Chevrolet Caprice and 2014 Chevrolet SS vehicles because windshield wiper motor gears may strip, causing wipers to stop working and reducing visibility.
Jomac is recalling 2009-2013 Ford F-350, F-450, and F-550 vehicles modified with specific PTO assemblies because oil leaks may cause a fire.
E. G. Emils & Sons is recalling Wegman's Organic Ham due to possible plastic contamination. No injuries have been reported.
Wolf Steel is recalling Napoleon GD3200-P and GD3200B-P propane gas fireplaces because the glass front can shatter, posing a laceration hazard.
General Motors is recalling 2013-2014 Chevrolet Cruze vehicles because the driver's air bag inflator may rupture in a crash, potentially causing serious injury.
Terex is recalling 2009-2013 aerial devices mounted on Ford Super Duty chassis because oil may leak onto the exhaust, increasing fire risk.
General Motors is recalling 2014 Chevrolet Corvettes because improper rear shock absorber welds may cause the tubes to separate, leading to sudden handling changes and increased crash risk.
Chrysler is recalling specific 2008-2010 Dodge and Chrysler vehicles because the ignition switch may move out of the run position, turning off the engine and disabling safety systems.
Roland is recalling approximately 640 RD-800 digital pianos because the AC power cord can be connected to XLR output jacks, posing an electrical shock hazard.
Mr. Wok Foods is recalling raw pork nuggets because they contain undeclared wheat, a known allergen.
Monroe Truck Equipment is recalling 2009-2013 Ford F-350, F-450, and F-550 trucks modified with specific PTO assemblies. Oil leaks from the PTO pressure switch may soak the exhaust thermal blanket, increasing fire risk.
Sherman Produce Co is recalling bulk shelled walnuts potentially contaminated with Listeria monocytogenes. The products were distributed in Missouri and Illinois.
Middle East Bakery is recalling Market Basket Dairy-Free, Gluten-Free Pancakes because they contain undeclared milk. The product was distributed to stores in New Hampshire and Massachusetts.
John W Hollis Inc is recalling Polidocanol 0.5% Solution for Injection because the products lack assurance of sterility.
Mitsubishi is recalling 2007-2013 Outlander vehicles because a power steering tube may leak fluid, potentially causing loss of steering assistance.
Sherman Produce Co is recalling Schnucks walnuts in 10 oz. plastic trays due to potential Listeria monocytogenes contamination. The product was distributed in Missouri and Illinois.
John W Hollis Inc is recalling compounded injectable products containing papaverine, phentolamine, and alprostadil due to a lack of assurance of sterility.
Mitsubishi is recalling 2007 and 2009 Outlander vehicles because a transfer case oil seal may dislodge, causing transmission fluid loss and potential loss of vehicle control.
Actavis Inc is recalling 6,913 packages of Vancomycin Hydrochloride Capsules because the drug is subpotent. The recall covers distribution across the United States.
John W Hollis Inc is recalling Methylcobalamin 1000 mcg injectable products because they lack assurance of sterility. The recall covers Lot # 1862 distributed nationwide.
John W Hollis Inc is recalling specific lots of Testosterone Cypionate for Injection because the products lack assurance of sterility.
John W Hollis Inc is recalling a compounded injectable drug product due to a lack of assurance of sterility. The product is distributed nationwide.
Setra is recalling 306 motorcoaches because an electrical overload in the light control unit may cause a short circuit or vehicle fire.
John W Hollis Inc. is recalling Lot 2868 of Polidocanol 1% Solution for Injection because the company cannot ensure the product is sterile.
John W Hollis Inc is recalling specific lots of Cyanocobalamin injection because the products lack assurance of sterility. The recall covers 2,650 mL distributed nationwide.
John W Hollis Inc is recalling specific lots of compounded injectable products containing papaverine, phentolamine, and alprostadil due to a lack of assurance of sterility.
John W Hollis Inc is recalling compounded Papaverine HCl and Phentolamine Mesylate injectable products due to a lack of assurance of sterility.
John W Hollis Inc is recalling Polidocanol 5% Solution for Injection because the company cannot ensure the product is sterile.
John W Hollis Inc is recalling specific lots of Liver Derivative Complex for injection due to a lack of assurance of sterility in the compounded aseptically filled products.
Daimler Trucks North America is recalling 2015 Freightliner trucks because axle manufacturing errors may create weak spots, increasing crash risk.
John W Hollis Inc is recalling B-Complex/Adenosine Injectable Solution due to a lack of sterility assurance in the compounded aseptically filled products.
John W Hollis Inc is recalling 80 mL vials of Lipotropic Gold injectable products because they may lack sterility assurance.
John W Hollis Inc is recalling compounded injectable products containing papaverine, phentolamine, and alprostadil due to a lack of sterility assurance.
John W Hollis Inc is recalling specific lots of compounded injectable products containing papaverine, phentolamine, and alprostadil due to a lack of sterility assurance.
John W Hollis Inc is recalling Pyridoxine HCl 100mg injectable products because they lack assurance of sterility. Consumers should stop using the product and contact their pharmacist.
John W Hollis Inc. is recalling Levocarnitine Solution for injection because the company cannot ensure the product is sterile. The recall covers specific lots distributed nationwide.
John W Hollis Inc is recalling MIC Plus B12 injectable vials because the products lack assurance of sterility. Consumers should stop using the affected lots immediately.
John W Hollis Inc. is recalling specific lots of Mannitol 5% Solution for injection because the products lack assurance of sterility.
Scott and Trek are recalling 2011-2013 bicycles with specific SR Suntour front forks that can break, posing a crash hazard.
Whole Foods Market Group Inc. is recalling 140 units of Thai Soba Noodle Salad because the product contains undeclared soy.
ConMed Corporation is recalling Altrus Thermal Tissue Fusion Handpieces due to a risk of burns. The recall covers 12,653 units distributed worldwide.
American Waffle is voluntarily recalling one lot of liveGfree Gluten Free Blueberry Pancakes because the product contains undeclared milk.
Brunkow Cheese of Wisconsin is recalling Fayette Creamery Jalapeno Raw Milk Cheddar Cheese because it contains an undeclared soy ingredient.
Boston Scientific is recalling 968 IntellaTip MiFi XP Temperature Ablation Catheters because some units were not manufactured according to specification.
Philips is recalling Ingenia HA FLEX TRAK Trolleys because the central column can clamp a patient's foot. The recall covers 420 units distributed worldwide.
American Importing Co, Inc is voluntarily recalling Cinnamon Crunch Granola because it may contain undeclared almonds, posing a risk to people with allergies.
Anhing Corporation is recalling Caravelle Chili Powder because it may be contaminated with Salmonella. The recall covers 83 cartons distributed nationwide.
Nellcor Puritan Bennett Inc. is recalling Backlight Inverter Printed Circuit Boards for PB840 Ventilators due to a potential loss of the graphical user interface display.
RaySearch Laboratories is recalling RayStation software version 4.0.3.4 due to a bug that causes incorrect dose calculations for radiation therapy plans with variable CT slice spacing.
Ebi, LLC is recalling 32 units of the Biomet Spine Cypher MIS Screw Inserter due to an increased rate of instrument tip failure.
GE Healthcare is recalling Compact Airway Modules because a loose screw may cause pump failure, leading to loss of respiratory gas monitoring.
Boston Scientific is recalling 968 IntellaTip MiFi XP Temperature Ablation Catheters because some units were not manufactured according to specification.
Nutri-West is voluntarily recalling Total Probiotics dietary supplements because raw materials may contain Chloramphenicol. The recall covers 13,864 bottles distributed nationwide and in England.
Ability Dynamics is recalling 175 RUSH81 prosthetic feet because existing bolts may be bottomed out in threaded holes, which could lead to bolt failure.
Spacelabs Healthcare is voluntarily recalling Ventilator Flexport Interfaces because the bedside monitor may display minute volume values up to ten times the actual value.
Julie Vos is recalling about 324 women's scarves because they fail to meet federal flammability standards, posing a risk of burn injury.
K & W Sausage is recalling specific sausage products because they contain undeclared soy and wheat, which are known allergens.
Elekta, Inc. is recalling Synergy XVI radiation therapy systems because they may incorrectly calculate the treatment table's target position.
Biomet is recalling G7 Acetabular System Positioning Guide Rods because they may fracture during surgery, potentially causing retained fragments or surgical delays.
Boston Scientific is recalling 968 IntellaTip MiFi XP Temperature Ablation Catheters because some units were not manufactured according to specification.
Philips is recalling Height Adjustable FlexTrak trolleys and Trolley Variable Height IRFs for Ingenia MR systems due to a risk of foot clamping.
Walmart is recalling 15 pairs of safety glasses that failed to meet required industrial lens thickness and lacked OSHA markings.
Coravin is recalling about 65,000 Wine Access Systems in the U.S. because bottles can break during use, posing a laceration hazard.
Biomet, Inc. is recalling 102 EZPass Suture Passers because the nitinol wire may buckle and become kinked, making the instrument difficult to use.
Ferring Pharmaceuticals is recalling TEV-TROPIN injection bottles due to potential silicone oil contamination from a leaking line during manufacturing.
Biomet is recalling G7 Acetabular System Positioning Guide Posts because the guide rod may fracture during surgery, potentially causing a delay in the procedure.
Rudolph Foods is recalling 34 pounds of pork cracklins because the product contains monosodium glutamate (MSG), which is not declared on the label.
Kodiak Wild Alaska Seafood is recalling 25 lb vacuum-packed Pacific Cod fillets because the firm distributed frozen seafood without a required operating permit or HACCP controls.
Boston Scientific is recalling IntellaTip MiFi XP Temperature Ablation Catheters because some units were not manufactured according to specification.
Synthes, Inc. is recalling external fixation systems because labeling changes were made to reflect updated protocols for Magnetic Resonance (MR) imaging safety designations.
Nipro Medical Corporation is recalling NIPRO Safe Touch Safety Scalp Vein Sets because a crack in the connector could cause fluid leakage.
Boston Scientific is recalling 968 IntellaTip MiFi XP Temperature Ablation Catheters because some units were not manufactured according to specification.
Elekta, Inc. is recalling MOSAIQ oncology software versions 1.40 through 2.50 because scrolling actions can unintentionally change direction selections.
Kodiak Wild Alaska Seafood is recalling 42 pounds of frozen Pacific halibut fillets because the firm operated without a required permit or HACCP controls.
Nutri-West is voluntarily recalling Total Enzyme and Total Probiotics supplements because raw materials may contain Chloramphenicol.
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products FS Calibrator 1 because calibrator values were assigned using a reference method that was not fully validated.
Roche Diagnostics is recalling cobas 6000 analyzer filters that may cause discrepant results and system alarms.
Biomet is recalling 100 units of EZPass Suture Retriever instruments because the nitinol wire may buckle and become kinked, making the device difficult to use.
Kerr Corporation is recalling one lot of Tytin Regular Set dental restorative material because it may set faster than specified in the Directions for Use.
Biomet is recalling 100 units of EZPass Nylon Monofilament Suture Passers because the internal wire may buckle, making the instrument difficult to use.
Children's Medical Ventures is recalling 112 infant apnea monitors due to a battery wire harness defect that renders the devices inoperable.
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 17 because calibrator values were assigned using a reference method that was not fully validated.
Elekta, Inc. is recalling 224 iGUIDE Systems because a software bug prevents the system from logging off. The recall covers units distributed worldwide.
Thorne Research is recalling Captomer capsules because they are marketed as dietary supplements but contain DMSA, an active drug ingredient, making them unapproved new drugs.
Boston Scientific is recalling 968 IntellaTip MiFi XP Temperature Ablation Catheters because some units were not manufactured according to specification.
Thorne Research is recalling Captomer-250 capsules because they are marketed as dietary supplements but contain DMSA, an active drug ingredient, making them unapproved new drugs.
Roche Diagnostics is recalling 462 Serum Work Area filters for the MODULAR ANALYTICS EVO analyzer due to potential loose components that may cause discrepant results and system alarms.
Roche Diagnostics is recalling cobas 8000 analyzer filters that may cause discrepant results, alarms, or foam under certain conditions.
The Manischewitz Company is recalling Tam Tams Snack Crackers Unsalted due to rancidity. The recall covers 29,413 cases distributed nationwide.
The Manischewitz Company is recalling Tam Tams Snack Crackers Original due to rancidity. The recall covers 29,413 units distributed nationwide.
Siemens Medical Solutions Diagnostics is recalling 19 VersaCell X3 robotic laboratory systems because the keyboard and monitor may not be properly secured to the monitor arm.
Gen-Probe Inc is recalling APTIMA Urine Collection Kits because inner pouches are mislabeled as swab collection kits.
The Manischewitz Company is recalling Tam Tams Snack Crackers in Onion flavor due to rancidity. The recall covers 29,413 units distributed nationwide.
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