Archive
481 recalls were announced in June 2015.
Of the 481 recalls this month scored against our rubric, 6% are Critical, 26% are Severe.
Which agencies issued them
Baby Jogger is recalling specific infant car seats because labels and manuals contain incorrect or missing safety information, which may increase injury risk in a crash.
Zimmer CAS is recalling 78 Tibial Alignment Guides because spikes may bend or break during use.
Silver Eagle is recalling 2014-2015 VAST-20N, VAST-20W, and CTL-40W converter dollies because a brake valve issue may cause brake drag and overheating.
Amy's Kitchen is recalling Gluten Free Vegetable Lasagna because supplier-confirmed Listeria monocytogenes was found in spinach used in the product.
Giant Eagle is recalling Apricot Filled Cookies sold over the counter because the labels failed to declare the milk allergen.
Amy's Kitchen is recalling Vegetable Lasagna products because supplier-confirmed Listeria Monocytogenes was found in spinach used in manufacturing.
Amy's Kitchen is recalling Brown Rice & Vegetables Bowls because a supplier notified them that spinach used in manufacturing contained Listeria monocytogenes.
Amy's Kitchen is recalling Stuffed Pasta Shells Bowls because supplier-confirmed Listeria monocytogenes was found in spinach used in manufacturing.
Amy's Kitchen is recalling Enchilada Verde products because a spinach supplier notified them that the ingredient contained Listeria monocytogenes.
Siemens Medical Solutions USA is recalling 131 syngo Workflow SLR systems because a software defect may cause order loss during restarts, leading to diagnosis delays.
Zimmer, Inc. is recalling 1,689 PRI Femoral Impactor Blocks because uncured adhesive may leak from the device, potentially causing a biological response in patients.
Zimmer, Inc. is recalling 4.5mm Cortical Screws for the M/DN system because they are not compatible with the device, potentially causing surgical complications.
Amy's Kitchen is recalling Gluten Free Tofu Scramble Breakfast Wraps because a spinach supplier notified them that the ingredient contained Listeria monocytogenes.
Amy's Kitchen is recalling Tofu Scramble because supplier-identified Listeria monocytogenes was found in spinach used for manufacturing.
Amy's Kitchen is recalling Tofu Vegetable Lasagna because a supplier notified them that spinach used in the product contained Listeria monocytogenes.
Amy's Kitchen is recalling Brown Rice & Vegetables Bowls because a supplier notified them that spinach used in manufacturing contained Listeria monocytogenes.
Frontier Natural Products Co-op is recalling Simply Organic Enchilada Sauce Seasoning packets due to potential Salmonella contamination. The product was distributed nationwide, to Puerto Rico, the Virgin Islands, Canada, and military channels.
Amy's Kitchen is recalling Garden Vegetable Lasagna because supplier-confirmed Listeria monocytogenes was found in spinach used during manufacturing.
Northhampton Peanut Company is recalling Ava's Berry Nutty Mix trail mix because it contains undeclared sulfites.
Synovis is recalling specific Vascu-Guard Peripheral Vascular Patch codes because users reported difficulty distinguishing the smooth from the rough surface.
Siemens Healthcare Diagnostics is recalling Dade Actin Activated Cephaloplastin Reagent because assay controls are out of assigned ranges, potentially causing inaccurate APTT test results.
Philips is recalling two Brilliance iCT Computed Tomography X-ray systems because a supplier torque wrench malfunction may have resulted in incorrect fastener torque.
Siemens Medical Solutions is recalling 167 units of Syngo.via and Syngo.x software because measurements on subsequent images do not appear on printouts.
MRP, LLC dba AMUSA is recalling 200,000 units of 0.9% Sodium Chloride Injection Flush Syringes because the labels display an incorrect expiration date.
Siemens is recalling 2,256 units of the Dimension Vista LOCI TSH test due to a defect that may cause falsely low results.
4 Him Food Group LLC is recalling Salted Caramel Premium Puffed Corn because the nutrition label incorrectly listed zero grams of sugar per serving.
Creative Food Concepts is recalling Coconut Water with Pineapple and Thai Lime because the company lacks a documented 5-log reduction process on file.
Northhampton Peanut Company is recalling Roche Brothers Berry Nutty Mix trail mix because it contains undeclared sulfites, a non-allergen.
Nidek Inc is recalling 114 EC-5000 Excimer Laser Corneal Surgery Systems because the multi-stage treatment option in the operator's manual was not approved by the FDA.
Guayaki S.R.P., Inc. is recalling one lot of Guayaki Brand Yerba Mate Revel Berry due to consumer complaints of fermented, slimy, carbonated, or moldy product.
Medtech Products is recalling Sucrets Sore Throat & Cough Vapor Cherry lozenges because an incorrect book label was applied to the tins.
Creative Food Concepts is recalling Invo Coconut Water with Pineapple because the product lacks a required 5 log reduction process.
Coreva Health Science is recalling ActCel Hemostatic Dressing because customer literature and websites promoted unapproved uses for controlling bleeding in body cavities.
Fresenius Kabi is recalling 5,488 bags of KABIVEN IV solution because the label lists 3.1% amino acids, but the product actually contains 3.3%.
Mylan Pharmaceuticals is recalling 7,722 bottles of Mycophenolic Acid Delayed-release Tablets, 180 mg, because they failed to meet dissolution specifications.
Teva Pharmaceuticals is recalling 889 bottles of Zebeta (bisoprolol fumarate) 10mg tablets because they failed dissolution specifications during stability testing.
Smiths Medical is recalling 15 BCI Advisor Vital Signs Monitors because their auxiliary serial ports may transmit incorrect data to collection systems.
Siemens Healthcare Diagnostics is recalling Factor IX plasma reagents for the BCS/BCS XP system due to erroneously high results at the lower end of the measuring range.
Edwards Lifesciences is recalling 978 Swan-Ganz CCO/Sv02/CEDV/VIP Thermodilution Catheters because they failed internal statistical tests for heparin activity.
Sandoz, Inc. is recalling specific lots of Cetirizine HCl Chewable Tablets because an impurity exceeded specifications during stability testing.
Ortho-Clinical Diagnostics is recalling VITROS Immunodiagnostic Products Signal Reagent, Lot 3082, because the reagent packs may contain blank labels.
Kalmar is recalling 2010-2014 Ottawa T2 tractors because a vent tube defect may allow engine oil to contact hot surfaces, increasing fire risk.
Forest River is recalling 1,497 model year 2016 trailers because wheel studs may break, potentially causing the wheel to detach and increasing crash risk.
Pali Design is recalling approximately 18,000 children's furniture units in the U.S. because a plastic restraint strap can break, allowing the furniture to tip over and cause injury or death.
General Motors is recalling 2015 Cadillac ATS and CTS vehicles because a brake pedal bracket may fracture, preventing the driver from applying the brakes.
Gulf Stream is recalling 2015 Canyon Trail and Sedona trailers because entry step rivets may shear, causing steps to fail and increasing the risk of falls.
Big Easy Foods is recalling approximately 93,006 pounds of raw and cooked stuffed chicken products because they contain wheat, an undeclared allergen.
Kia is recalling 2011 Sportage vehicles because the brake light switch may fail, preventing brake lights from illuminating and increasing crash risk.
Vermeer is recalling specific 2015 TLR30HD and TLR30LD trailers because an incorrectly installed safety chain may fail to prevent the trailer from separating from the tow vehicle.
Fontaine is recalling 2016 Revolution semi-trailers because hardened washers may crack, potentially causing structural detachment and increasing crash risk.
Mercedes-Benz is recalling specific 2015 E250, GLK250, and ML250 vehicles because oil may leak from the chain tensioner gasket, creating a fire hazard.
Benedetti Farms is recalling approximately 11,670 pounds of chicken and turkey sausage products because hog and sheep casings were not listed on the labels.
Prevost is recalling 2015 X3-45 and H3-45 coaches because front suspension bolts may fail, potentially causing loss of vehicle control.
Prevost is recalling 314 X3-45 coaches from 2006-2010 because rusted booster studs may break, allowing power cables to short against the frame and cause a fire.
Nova Bus is recalling 250 model year 2001-2004 LFS buses because incorrectly connected air hoses may delay parking brake application, increasing crash risk.
Bariatric Fusion is recalling cherry-flavored iron soft chews because the packaging fails to meet child-resistant closure requirements, posing a risk to young children.
Prevost is recalling 452 model year 2010-2014 coaches because engine heat may damage fire suppression wires, potentially causing an engine shutdown and crash.
Quincy Street, Inc. is recalling approximately 49,308 pounds of pork sausage products that may be contaminated with foreign materials. The products were shipped to institutions nationwide.
Demes Gourmet Corp. is recalling approximately 29,052 pounds of chicken longanisa because the products were wrapped in hog casings not listed on the labels.
Cree Inc. is recalling approximately 700,000 LED T8 replacement lamps sold in the U.S. because electrical arcing can cause the lamps to overheat and melt, posing a burn hazard.
Big Lots is recalling about 16,000 hanging chairs because they can tip over and cause falls. Consumers should stop using them and return the base for a refund.
Hospira is recalling 24,744 bags of Lactated Ringer's Irrigation due to confirmed mold contamination. The product was distributed nationwide.
The Santa Barbara Smokehouse is recalling Channel Island Old Fashioned Smoked Atlantic Salmon due to potential Listeria monocytogenes contamination.
The Santa Barbara Smokehouse is recalling specific lots of smoked Atlantic salmon due to potential Listeria monocytogenes contamination.
Conway Import Co. is voluntarily recalling Organic Sesame Ginger Dressing because it may contain Salmonella.
Strohecker's Pharmacy is recalling 365 vials of Testosterone Cypionate 200 mg/mL because they contain Estradiol Valerate 20 mg/mL instead.
Sun Rich Fresh Foods is recalling Sub Way Apple Slices due to potential contamination with Listeria monocytogenes. The product was distributed to retail and food service locations in nine states.
Tyson Fresh Meats is recalling approximately 16,000 pounds of ground beef products due to possible E. coli O157:H7 contamination. The products were shipped to one distribution location in New York.
Sun Rich Fresh Foods Inc is recalling Sun Rich Apple Slices with Caramel Dip due to potential Listeria monocytogenes contamination.
Sun Rich Fresh Foods Inc is recalling fresh cut mixed apple slices due to potential Listeria monocytogenes contamination. The product was distributed to retail and food service locations in nine states.
Sun Rich Fresh Foods Inc is recalling fresh cut red apple slices due to potential Listeria monocytogenes contamination. The product was distributed to retail and food service locations in nine states.
Philips Medical Systems is recalling 153 Brilliance CT 40 systems because the patient couch may unexpectedly descend to its lowest point during an exam.
The Santa Barbara Smokehouse is recalling Channel Island Smoked Gravadlax Salmon due to potential Listeria monocytogenes contamination.
The Santa Barbara Smokehouse is recalling specific lots of smoked salmon due to potential Listeria monocytogenes contamination.
Advanced Physician Solutions is recalling Sodium Tetradecyl Injectable vials nationwide because the company cannot ensure the product is sterile.
Advanced Physician Solutions, Inc. is recalling Glycerin (Sterile Water) 100ml 71% Injectable vials nationwide due to a lack of assurance of sterility.
Advanced Physician Solutions is recalling 77 vials of Cyanocobalamin injectable nationwide due to a lack of assurance of sterility.
Toyota is recalling 3,013 2015 Lexus NX200t vehicles because a damaged ABS actuator component may cause loss of vehicle stability and increase crash risk.
Timken is recalling aftermarket front wheel bearings with incorrect dimensions for 2001-2012 Ford Escape, 2001-2011 Mazda Tribute, and 2005-2011 Mercury Mariner vehicles due to crash risk.
Strange Engineering is recalling specific Modified Street Axles because post-manufacturing heat treatment may have reduced their strength, increasing the risk of axle failure and vehicle crashes.
Daimler Trucks North America is recalling 746 Thomas Built Buses Saf-T-Liner HDX school buses due to a defect that may cause engine oil to contact hot surfaces, increasing fire risk.
Daimler Trucks is recalling 3,200 trucks and buses due to a defect that may allow engine oil to contact hot surfaces, increasing the risk of fire.
Conway Import Co. is voluntarily recalling Citrus Organic Vinaigrette Dressing because it may contain Salmonella.
Advanced Physician Solutions is recalling Nanpyridoxine (Sterile Water) 30ml 50mg/ml injectable vials because the product lacks assurance of sterility.
Advanced Physician Solutions, Inc. is recalling 32 vials of Nandrolone Decanoate Injectable due to a lack of assurance of sterility. The product was distributed nationwide.
Advanced Physician Solutions is recalling 416 prefilled syringes of Sodium Hyaluronate Injectable because the company cannot guarantee the product is sterile.
Advanced Physician Solutions is recalling 21 vials of Sodium Hyaluronate Injectable due to a lack of assurance of sterility. The product was distributed nationwide.
Advanced Physician Solutions, Inc. is recalling Estradiol Cypionate injectable vials because the FDA determined there is a lack of assurance of sterility.
Advanced Physician Solutions is recalling 41 vials of 50% DMSO Injectable Solution because the company cannot assure the product's sterility.
Advanced Physician Solutions is recalling Estradiol Valerate Injectable because the product lacks assurance of sterility.
Advanced Physician Solutions, Inc. is recalling injectable glutathione vials because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Advics is recalling specific antilock brake system actuators manufactured in December 2014 due to contamination that may affect valve function and vehicle stability.
Sun Rich Fresh Foods Inc is recalling 10 lb. Sunshine Salad Kits due to potential Listeria monocytogenes contamination. The product was distributed to retail and food service locations in nine states.
Advanced Physician Solutions is recalling Hydroxyzine Hydrochloride Injectable vials because the FDA identified a lack of assurance of sterility.
Advanced Physician Solutions, Inc. is recalling Sodium Tetradecyl Sulfate (Sterile Water) 3.5% Injectable due to a lack of assurance of sterility.
Advanced Physician Solutions is recalling Hydroxyprogesterone Caproate injectable vials because the company cannot ensure the product is sterile.
Advanced Physician Solutions, Inc. is recalling Hydroxyzine Hydrochloride Injectable because the product lacks assurance of sterility. The recall covers 3 vials distributed nationwide.
Advanced Physician Solutions is recalling Estradiol Cypionate injectable vials because the product lacks assurance of sterility.
Advanced Physician Solutions is recalling 17 vials of Estradiol Valerate Injectable because the FDA determined there is a lack of assurance of sterility.
Advanced Physician Solutions is recalling Vitamin D3 (Olive Oil) 50,000 Units/mL Injectable due to a lack of assurance of sterility.
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