Archive
653 recalls were announced in May 2015.
Of the 653 recalls this month scored against our rubric, 8% are Critical, 22% are Severe.
Which agencies issued them
Arc Medical Inc is recalling 1,810 units of ThermoFlo 1 HME because the outer shipping carton displayed an incorrect expiry date, although the inner product carton was labeled correctly.
Apotex Inc. is voluntarily recalling 5,352 bottles of Olanzapine 20 mg tablets because the drug was found to be subpotent.
Cipla Limited is recalling 140,625 vials of Levalbuterol Inhalation Solution because the product failed impurity specifications. The affected lot is distributed nationwide.
Medtech Products, Inc. is recalling Monistat 1 Simple Cure because the distributed units lack the required topical cream.
Zimmer Surgical Inc is recalling 36 units of the 100 mL Hemovac Mini Evacuator because the shipper carton contained only one Instructions for Use (IFU) instead of one per sales unit.
NABI is recalling 2007-2015 LFW, BRT, and 2007-2013 CLFW transit buses because a vent tube may detach, allowing engine oil to contact hot surfaces and cause a fire.
Blue Bird is recalling 840 school buses due to a defect that may allow engine oil to contact hot surfaces, increasing fire risk.
Blue Bird is recalling 2009-2016 All American non-school buses due to a defect that may allow engine oil to contact hot surfaces, increasing fire risk.
Tiffin is recalling specific 2015 Allegro and Phaeton motorhomes because moisture may cause slide-out sections to extend while driving, increasing crash risk.
Kaldi's Coffee Roasting is recalling about 700,000 disposable paper cup sleeves because they can ignite in microwaves. Two fire incidents were reported, with no injuries.
Precision Trading is recalling about 4,700 PREMIUM Espresso Makers because the filler cap can crack or pop off, releasing steam and posing a burn risk.
Rocky Brands is recalling approximately 1,800 rubber hunting boots because the snake guard can fail to protect the wearer's feet from a snake bite.
Gillig is recalling 2014-2015 Low Floor buses because taillight brackets may detach, reducing visibility and increasing crash risk.
Takata is recalling specific frontal passenger air bag inflators for certain Honda and Mazda vehicles due to a risk of rupture during deployment.
Takata is recalling specific frontal driver air bag inflator modules that may rupture during deployment, potentially causing serious injury or death.
Takata is recalling specific passenger frontal air bag inflators for 2001-2008 vehicles due to a risk of rupture during deployment.
Autocar is recalling 2011-2016 Xpeditor vehicles because the parking brake may engage unexpectedly at any speed, increasing crash risk.
Chrysler is recalling 2014-2015 RAM 4500 and 5500 trucks because their tires are rated for a lower speed than the vehicle's maximum capability, posing a crash risk.
ZYK Enterprises is recalling 2,522 pounds of boneless veal trim and whole muscle cuts due to possible E. coli O157:H7 contamination. The products were distributed to wholesale establishments in California, Massachusetts, and Washington.
Takata is recalling PSPI-L passenger air bag inflators in specific Honda, Toyota, Pontiac, and Subaru models. The inflators may rupture in a crash, sending metal fragments into the vehicle.
New Flyer is recalling certain 2008-2014 buses because a vent tube may detach, allowing engine oil to contact hot surfaces and increase fire risk.
Chrysler is recalling 2013-2015 Fiat 500 electric vehicles because a software issue may cause the transmission to unexpectedly shift to neutral, increasing crash risk.
TenPoint Crossbow Technologies is recalling about 127,000 crossbows because they may fire unexpectedly after the safety is re-engaged, posing an injury risk.
A.S.K. Foods is recalling 414 pounds of Wegmans Herb Stuffing with Pork and Veal because the product contains undeclared soy lecithin.
Nissan is recalling specific 2001-2006 models because the passenger air bag inflator may rupture during deployment, potentially sending metal fragments into the vehicle.
Industrial Axle Company is recalling specific ALKO AXIS trailer axles because wheel mounting studs may fail, potentially causing wheel separation and increasing crash risk.
Daimler Buses North America is recalling 2007-2012 Orion VII natural gas buses because engine oil may contact hot surfaces, increasing fire risk.
AA Poultry Processing is recalling chicken and turkey products contaminated with trichloro-s-triazinetrione, an unapproved substance.
La Terra Fina is recalling specific lots of Chunky Spinach Artichoke & Parmesan Dip because the chopped spinach ingredient tested positive for Listeria monocytogenes.
REFA Enterprises is recalling Forever Beautiful Bee Pollen capsules because FDA analysis found the product contains sibutramine and phenolphthalein.
La Terra Fina is recalling Organic Thick & Creamy Spinach Dip and Spread because the chopped spinach ingredient tested positive for Listeria monocytogenes.
REFA Enterprises is recalling Forever Beautiful INFINITY capsules because FDA analysis found the product contains sibutramine and phenolphthalein without an approved NDA/ANDA.
Spiceco is recalling Pride of Szeged Sweet Hungarian Paprika because it may contain undeclared peanut protein. The recall includes additional products containing the implicated paprika.
Detox Transforms is recalling iNDiGO capsules because they contain undeclared phenolphthalein, making the product an unapproved drug.
The FDA is recalling HALO-70 MEGA MASS BUILDER capsules because they contain an unapproved synthetic hormone ingredient, making them unapproved new drugs.
Detox Transforms is recalling EDGE Amplified Weight Release capsules because the product contains undeclared phenolphthalein and fluoxetine, making it an unapproved drug.
The FDA is recalling iNSANE Bee Pollen capsules because they contain undeclared phenolphthalein and fluoxetine, making them unapproved drugs.
Physician Preferred Medical, LLC is recalling Epel 18 mg Estradiol Pellets because the specific lot failed sterility testing. The product was distributed in Arizona and Kansas.
Detox Transforms is recalling AMPD GOLD Bee Pollen capsules because they contain undeclared sildenafil, making them unapproved drugs.
Anabolic Science Labs is recalling SWOLL-250 Super Mass Builder Quad Stack capsules because they contain unapproved synthetic hormone ingredients.
Anabolic Science Labs LLC is recalling Estrastain Pro-Anabolic Mass and Hardening Complex capsules because they contain unapproved synthetic hormone ingredients.
Ultra ZX Labs is recalling Ultra ZX dietary supplements because FDA testing found undeclared sibutramine and phenolphthalein. The product was marketed without an approved NDA or ANDA.
Toyota is recalling approximately 1.97 million vehicles, including Pontiac, Lexus, and Toyota models, to replace passenger air bag inflators that may rupture.
The FDA is recalling 7-Ment Alpha Advanced Mass Builder capsules because they contain an unapproved synthetic hormone ingredient.
Hospira Inc. is recalling 9,912 units of 0.9% Sodium Chloride Injection, USP, 250 mL, because human hair was found floating in the IV solution.
Anabolic Science Labs is recalling Professional Formexx Black capsules because they contain an unapproved synthetic hormone ingredient.
Best Foods NJ, Inc. is recalling Deer Brand Golden Raisins because they contain undeclared sulfites, a potential allergen.
La Terra Fina is recalling Spinach Artichoke & Parmesan Dip made with Greek Yogurt because a supplier notified the firm that the product contained IQF chopped spinach that tested positive for Listeria Monocytogenes.
The FDA is recalling M1-Alpha Labs Mega Mass Builder capsules because they contain an unapproved synthetic hormone ingredient, making them unapproved new drugs.
Toyota is recalling 2004-2005 RAV4 vehicles because the driver's air bag inflator may rupture during deployment, posing a risk of serious injury or death.
Forest River is recalling 226 model year 2014-2015 Glaval transit buses because a loose tie rod jam nut may cause loss of control.
International Foodsource, LLC is recalling ground cumin that may contain peanut protein. The product was distributed in Illinois, Massachusetts, Maryland, and Virginia.
Autocar is recalling 2014-2016 Xpert and XSpotter vehicles because a vent tube defect may allow engine oil to contact hot surfaces, increasing fire risk.
Toyota is recalling specific 2002-2007 Lexus, Toyota, and Pontiac vehicles because the front passenger air bag inflator may rupture during a crash, potentially causing serious injury or death.
Autocar is recalling 2008-2016 Xpeditor vehicles because a vent tube may detach, allowing engine oil to contact hot surfaces and increase the risk of a vehicle fire.
Detox Transforms is recalling BtRiM Max capsules because they contain undeclared phenolphthalein, making the product an unapproved drug.
The FDA is recalling M14-Ment Advanced Mass Builder capsules because they contain an unapproved synthetic hormone ingredient, making them unapproved new drugs.
Viewray Incorporated is recalling one ViewRay System due to a software error affecting coordinate correction for non-standard patient positions.
Royal Frozen Food is recalling Blintzes with Cherry because the product contains undeclared milk. The recall affects 3,600 units distributed in California and Nevada.
Royal Frozen Food is recalling Blintzes with Potato because they contain undeclared milk. The recall affects 3,600 units distributed in California and Nevada.
SM Fish Corp is recalling Ossie's Pickled Lox & Cream because it contains undeclared eggs, a sub-ingredient of the mayonnaise.
Chrysler is recalling 2015 Dodge Challengers because a loose or missing rear mounting bolt on the driver's side air bag curtain may increase injury risk in a crash.
Spiceco is recalling Better Valu Chicken Seasoning and Pride of Szeged Sweet Hungarian Paprika because they may contain undeclared peanut protein.
Cott Beverages is recalling Uforce Q40 Tropical Mango Energy Drink because it may contain a trace amount of walnut, a tree nut not listed on the ingredient label.
Cott Beverages Inc. is recalling Rey Panama Tropical Mango because it may contain a trace amount of walnut, a tree nut not listed on the ingredient label.
Cott Beverages Inc. is recalling Sunny Select Mango Guava because it may contain trace amounts of walnuts, a tree nut not listed on the ingredient label.
SM Fish Corp is recalling Ossie's Pickled Lox Dairy due to undeclared milk. The product was distributed in New York and New Jersey.
Spiceco is recalling Hytop Seasoned Salt because it may contain undeclared peanut protein. The recall includes specific lot numbers distributed nationwide and abroad.
Whole Foods Market is recalling Health Starts Here Rye Bread in Texas, Oklahoma, Arkansas, and Louisiana due to undeclared wheat.
Taylor Farms Florida is recalling Wawa brand Kale and Quinoa Salad because the packaging fails to declare soy as an ingredient.
Spiceco is recalling specific lots of chicken seasoning and sweet Hungarian paprika because they may contain undeclared peanut protein.
Sazon, Inc. is recalling Sazon with Saffron because the cumin used was contaminated with peanut protein. The product was distributed in eight states and Puerto Rico.
Spiceco is recalling Redner's Chicken Rub and Sweet Hungarian Paprika because they may contain undeclared peanut protein.
SM Fish Corp is recalling 266 units of Ossie's Herring in Sour Cream due to undeclared milk. The product was distributed in New York and New Jersey.
Spiceco is recalling Sylvia's Sizzlin' Hot Spice because it may contain undeclared peanut protein. The recall includes additional products using the implicated paprika.
Cott Beverages Inc. is recalling Clear Choice Diet Orange Mango because it may contain a trace amount of walnut, a tree nut not listed on the ingredient label.
Philips is recalling EPIQ 7 Ultrasound Systems with the Pediatric Cardiology option because a unit conversion error may cause incorrect Body Surface Area calculations.
ICU Medical is recalling specific MicroClave T-Connectors because they may separate, causing fluid leakage. The recall affects 250 units distributed in nine US states.
Spiceco is recalling Pride of Szeged Fish Rub Seasoning because it may contain undeclared peanut protein. The recall includes additional products using the implicated paprika.
Spiceco is recalling Emeril's Blackened Seasoning Blend because it may contain undeclared peanut protein. The recall includes 2,483 cases distributed nationwide and abroad.
Sazon, Inc. is recalling Sazon Coriander & Annatto because the cumin used was contaminated with peanut protein. Consumers should check their pantry for the affected lots.
Cott Beverages is recalling Uforce R140 Tropical Mango Energy Drink because it may contain trace amounts of walnuts, a tree nut not listed on the ingredient label.
Cott Beverages is recalling Clear Splash Orange Mango beverages because they may contain a trace amount of walnut, a tree nut not listed on the ingredient label.
Sazon, Inc. is recalling Sazon Coriander & Annatto Low Sodium because the product contains undeclared peanut protein. Consumers with peanut allergies should not consume the product.
Eos Imaging Inc is recalling 13 EOS digital radiography systems because a software alert regarding X-ray beam filtration may be suppressed, potentially leading to improper filtration during exams.
Royal Frozen Food is recalling Blintzes with Potato & Mushroom because they contain undeclared milk. The recall affects 3,600 units distributed in California and Nevada.
ICU Medical is recalling MicroClave T-Connectors because potential connection separation issues could lead to leakage.
ICU Medical is recalling 50 units of 98-inch Transfer Sets because potential connection separation could lead to leakage.
Spiceco is recalling unlabeled seasoned salt and Sweet Hungarian Paprika because they may contain undeclared peanut protein.
Cott Beverages is recalling Quick Strike Tropical Mango because it may contain a trace amount of walnut, a tree nut, which is not listed on the ingredient label.
Mitsubishi Heavy Industries is recalling 11 MHI-TM2000 Linear Accelerator Systems due to a software defect that allows radiation delivery despite communication errors and prevents saving treatment records.
ICU Medical is recalling specific MicroClave T-Connectors because they may separate, causing fluid leakage.
Bard Peripheral Vascular Inc is recalling 7,995 Bard MAX-CORE Disposable Core Biopsy Instruments due to a risk of self-activation-related issues.
B. Braun Medical is recalling specific pain control trays because a potential hole in the outer tray may compromise the sterile barrier, posing a risk of contamination.
ICU Medical is recalling 1,500 MicroClave T-Connectors because potential connection separation issues could lead to leakage.
ICU Medical is recalling 5,100 units of MicroClave T-Connectors because potential connection separation issues could lead to leakage.
Siemens is recalling 43 Axiom Aristos FX radiography systems because a cable cart defect could cause the cable holder to drop and hit patients or operators.
Stryker Instruments is voluntarily recalling specific wound drain and ambulating bulb products due to a potential sterility breach in the packaging.
ICU Medical is recalling MicroClave T-Connectors because potential connection separation issues could lead to leakage.
Giant Eagle is recalling store-cut Fontal cheese because it contains lysozyme, an egg allergen, that was not declared on the label.
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