Archive
772 recalls were announced in March 2016.
Of the 772 recalls this month scored against our rubric, 4% are Critical, 22% are Severe.
Which agencies issued them
Picnic Gourmet Spreads LLC is recalling Moroccan Cilantro Cheese Spread after testing revealed the presence of Listeria monocytogenes.
Winnebago is recalling certain 2015-2016 Adventurer and Itasca Suncruiser vehicles because hitch bolts were not properly torqued, which could cause the hitch to detach and increase crash risk.
Mack is recalling 2016-2017 Titan trucks because a steering shaft bolt may fail, causing loss of steering and potential crashes.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate and Bupivacaine HCL syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Hydromorphone HCL and Bupivacaine HCL syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Baclofen 5000 mcg/ml syringes because the agency could not ensure the product was sterile.
Hartley Medical Center Pharmacy is recalling Sufentanil Citrate/Clonidine/Bupivacaine syringes because the agency could not ensure the product was sterile.
Hartley Medical Center Pharmacy is recalling specific hydromorphone and baclofen syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Sufentanil Cit 1000 mcg/ml/Baclofen 300 mcg/ml syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate 10 mg/ml syringes due to a lack of assurance of sterility. The product was distributed nationwide.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate 20 mg/ml syringes due to a lack of assurance of sterility. The product was distributed nationwide.
Hartley Medical Center Pharmacy is recalling specific hydromorphone and bupivacaine syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Hydromorphone HCL 25 mg/ml syringes due to a lack of assurance of sterility. The product was distributed nationwide.
Picnic Gourmet Spreads LLC is recalling Tandoori Garlic Cheese Spread after Maryland health officials detected Listeria monocytogenes in a related product.
Terex is recalling 2015-2016 aerial devices and digger derrick lifts because the suspension circuit can inflate air bags, lifting outriggers and increasing injury risk.
Whole Foods Market is recalling Key Lime Squares sold in California after customers found metal shavings around the perimeter of the product.
Whole Foods Market is recalling Crazy for Cream cheese Brownies because metal shavings were found around the perimeter of the product.
GE Lighting is recalling high-intensity LED lamps because they can separate from their base and fall, posing an impact hazard. No injuries have been reported.
Sedecal S.A. is recalling 349 mobile X-ray systems because static electricity and other issues can cause uncommanded movements.
Bard Peripheral Vascular is recalling Denali Filter Delivery Systems because stop cocks may crack.
Gi Supply is recalling Large Volume Paracentesis Kits because the pinch clamp on the RP Bag may be missing, posing a splash hazard to users.
SRAM is recalling Zipp 88 aluminum front hubs because the flanges can fail, posing a crash and injury hazard. Consumers should stop using the hubs and contact SRAM for a free replacement.
Spacelabs Healthcare is recalling Xhibit Central Station units because patient height and weight values may be switched, causing incorrect Body Surface Area calculations.
Abbott Vascular is recalling the MitraClip Clip Delivery System because a mandrel fracture may prevent the clip from detaching during implantation.
Philips Respironics is recalling approximately 104,508 Trilogy and Garbin ventilators due to a software issue. The recall covers units distributed nationwide and internationally.
Value Plastics is recalling 33,000 custom tubing extensions because the parts may crack. The devices were distributed to three consignees in New York, Pennsylvania, and Minnesota.
Biomet is recalling 21,268 Crosslock DVR ePAK surgical sets because components may oxidize during storage. This could cause an inflammatory reaction if material enters the surgical wound.
Whole Foods Market is recalling Brownie Double Trouble brownies after a customer found metal shavings around the perimeter of the product.
Arrow International Inc. is recalling Super Arrow-Flex Percutaneous Sheath Introducer Sets because packaging damage may compromise sterility, posing a potential infection risk.
Whole Foods Market is recalling Peanut Butter & Yah Brownies because metal shavings were found around the perimeter of the product.
Arrow International is recalling FiberOptix Ultra 8 IAB devices because the sheath body may separate from the hub, posing a risk of bleeding.
East-West Specialty Sauces is recalling Classic Sweet & Sour Sauce because Zesty Orange sauce was mislabeled, posing a wheat and soy allergen risk.
Arrow International is recalling UltraFlex IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.
Arrow International is recalling Ultra 8 IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.
Giant Eagle is voluntarily recalling Japanese Breaded Cod Fillets sold in Pennsylvania and Ohio because they contain an undeclared soy allergen.
Urban Oven, LLC is recalling specific cookie varieties because the label fails to declare milk, a major food allergen, derived from butter.
Eastland Food Corporation is recalling Maesri Brand Shrimp Powder because it contains FD&C Yellow #6, which is not listed on the label.
Cary's of Oregon LLC is recalling Dark Chocolate Almond Toffee with Hawaiian Salt because the packaging fails to declare soy in the 'Contains' statement.
Whole Foods Market is recalling Salted Caramel Swirl Brownies after a customer found metal shavings around the perimeter of the product.
Urban Oven, LLC is recalling four varieties of cookies because the label fails to declare milk, an ingredient present in the butter used.
Urban Oven, LLC is recalling specific cookie varieties because the label fails to declare milk, an ingredient present in the butter used.
Picnic Gourmet Spreads LLC is recalling Parmesan Cheese Spread after testing revealed the presence of Listeria monocytogenes.
T.F. Foods is recalling specific lots of Bean Snacks because they contain undeclared peanut allergen. The affected products were distributed in New York and California.
Whole Foods Market is recalling Raspberry Brownies sold in California after a customer found metal shavings around the product.
Brett Anthony Foods is recalling Tofu Curry Cous Cous Salad because the label fails to declare peanuts, soy, and eggs.
Ingredion Incorporated is recalling food-grade cornstarch because it may contain metal fragments up to 50 mm in length.
SRAM is recalling Zipp bicycle quick releases because they may fail to engage, posing crash and injury hazards to riders.
Arrow International is recalling FiberOptix Ultra 8 IAB devices because the sheath body may separate from the hub, creating a risk of bleeding.
Bard Peripheral Vascular is recalling Denali Filter Delivery Systems because stop cocks may crack.
Ventura Foods LLC is recalling Land O Lakes margarine cups because they were distributed without labels, failing to disclose milk and soy allergens.
Urban Oven, LLC is recalling specific cookie varieties because the label fails to declare milk, an ingredient present in the butter used.
The Kroger Co is recalling King Soopers City Market Gourmet Bread Pudding due to undeclared walnuts. The product was distributed in Colorado and Utah.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate, Sufentanil Citrate, and Bupivacaine HCL vials due to a lack of assurance of sterility.
Becton Dickinson is recalling 250 units of the BD Intelliport Medication Management System Sensor because the sterility of the product cannot be assured, posing an increased risk of infection.
Ortho-Clinical Diagnostics is recalling VITROS 350 Chemistry Systems due to increased error codes when using specific calibrators.
GE Medical Systems is recalling 817 CT and PET CT scanner systems worldwide because service manuals contained incorrect torque values.
CooperSurgical, Inc. is recalling two units of Milex Arcing Diaphragms (Model MXWS95) because they contain an incorrect size diaphragm.
CMP Industries is recalling Impak Acrylic Resin Liquid, Lot 103113, due to potential rust discovered during an FDA inspection.
Zimmer Biomet is recalling a specific lot of M/L Taper Hip Prostheses because the device was incorrectly etched as 'STD' instead of 'EXT', although the packaging is correct.
Verathon is updating manuals for BladderScan and AortaScan devices to clarify they are not for diagnosing abdominal aortic aneurysms.
Golden State Medical Supply Inc. is recalling specific lots of Atorvastatin Calcium 10 mg tablets due to failed impurities and degradation specifications.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Calibrator E packs due to bias in the testosterone assay. The recall covers 519 packs distributed worldwide.
GE Medical Systems is recalling 522 CT and PET CT scanners worldwide because service manuals contained incorrect torque values.
Dollar Only Wholesale is recalling Strawberry Wafers because they may contain undeclared FD&C Red #3 and Yellow #6.
Ortho-Clinical Diagnostics is recalling VITROS 4600 Chemistry Systems because they may generate specific error codes when used with a recalled Calibrator Kit 9 lot.
Verathon is recalling GlideScope Titanium single-use video laryngoscope blades because the video image may flicker or distort during use.
Whole Foods Market is recalling specific brownies because metal shavings were found around the perimeter of the product.
DEOLEO USA is recalling specific bottles of Bertolli and Carapelli Extra Virgin Olive Oil due to trace amounts of pesticides not permitted in the US.
Reily Foods is recalling Carroll Shelby White Chicken Chili kits because the label incorrectly stated 0 mg sodium per serving instead of 590 mg.
Ortho-Clinical Diagnostics is recalling VITROS 5600 Chemistry Systems due to increased error codes when using a specific calibrator kit.
Philips is recalling 196 Allura Xper X-ray systems because they may display a 'Fluoro failed' error message when initiating fluoroscopy.
Biomet is recalling Verso Shoulder Forked Retractors because they were manufactured with 420 stainless steel instead of the specified 420 S29 material.
TEM Systems Inc is recalling ROTROL P Control quality control material due to customer complaints about failed target ranges for alpha angle.
Ecolab is voluntarily recalling 706 bottles of Scrub-Stat 4% Chlorhexidine Gluconate Foam Solution because the product is subpotent.
GE Medical Systems is recalling 324 CT and PET CT scanners worldwide because service manuals contained incorrect torque values.
Ortho-Clinical Diagnostics is recalling VITROS 5,1 FS Chemistry Systems due to increased error codes generated when using a specific calibrator lot.
ConforMIS, Inc. is recalling a specific unit of the iTotal Cruciate Retaining Knee Replacement System because an incorrect femoral component was distributed.
Ormco is recalling TF Adaptive Gutta Percha Points because the inner label is misidentified as ML3, though the outer package correctly identifies the product as SM3.
Ortho-Clinical Diagnostics is recalling VITROS 250 Chemistry Systems due to increased U90-382 or 6LU condition codes generated when using Calibrator Kit 9, Lot 954.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Calibrator E lots 42 and 43 due to bias in the testosterone assay.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Calibrator E lots 42 and 43 because they show bias in the testosterone assay.
Beckman Coulter is recalling iChem VELOCITY urine chemistry systems and strips because loose or missing analyte pads may go undetected by the system.
Medtronic is recalling one O-arm O2 Imaging System unit in Austria because loose screws may cause the detector panel to contact other parts, leading to noise, vibration, and poor image quality.
GE Medical Systems is recalling 25 CT and PET CT scanner systems because their service manuals contain an incorrect torque value.
GE Medical Systems is recalling specific CT and PET CT scanners because service manuals contained an incorrect torque value.
Golden State Medical Supply Inc. is recalling Atorvastatin Calcium 40 mg tablets due to failed impurities and degradation specifications.
GE Medical Systems is recalling 104 CT and PET/CT scanners worldwide because service manuals contained incorrect torque values.
Golden State Medical Supply is recalling specific lots of Atorvastatin Calcium 20 mg tablets due to failed impurities and degradation specifications.
Golden State Medical Supply Inc. is recalling specific lots of Atorvastatin Calcium 80 mg tablets because they failed impurity and degradation specifications.
Lakota is recalling 2016 Bighorn and Charger recreational vehicles because screws attaching the expanding room may fail, allowing it to extend unintentionally while driving.
Franklin Fueling Systems is recalling gas station hose and swivel fitting sets because the fitting can separate, causing fuel leaks and fire hazards.
Cooper Tire & Rubber Co. is recalling specific Roadmaster RM234 tires due to a potential sidewall hole that could cause sudden tire failure.
Nissan is recalling 46,671 model year 2014 Rogue vehicles because a fuel pump defect may cause the vehicle to stall without warning, increasing the risk of a crash.
General Motors is recalling 2016 Chevrolet Malibus because side air bag weld studs may fracture, increasing injury risk during deployment.
Stallion Bus is recalling 12 model year 2013 900 series transit buses because the wiper system may lose power, reducing visibility and increasing crash risk.
Ricon is recalling specific wheelchair lift models because platform side plates may crack or bearings may shift, creating a risk of the platform falling on the operator.
Room & Board is recalling Doyle arm and side chairs because the backrest can break during normal use, posing a laceration hazard.
Forest River is recalling specific Amera-Lite, Cargo Mate, Continental Cargo, and US Cargo trailers because incorrect tire pressure labels may lead to underinflation and tire failure.
Nestle USA is recalling specific chicken pizza and lasagna products due to possible glass contamination. No illnesses have been reported.
Pierce is recalling 267 emergency vehicles due to improperly installed heater hose clamps that may leak coolant, causing electrical shorts, vehicle stalls, or burn injuries.
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