Archive
1,183 recalls were announced in July 2015.
Of the 1,183 recalls this month scored against our rubric, 29% are Critical, 19% are Severe.
Which agencies issued them
Stradis Healthcare is recalling surgical Set Up Packs because they contain Devon Light Gloves that Medtronic is recalling.
Stradis Healthcare is recalling Blepharoplasty Packs because they contain Devon Light Gloves, which are subject to a separate recall by Medtronic.
Stradis Healthcare is recalling ENT Packs containing Devon Light Gloves due to a manufacturer recall of the glove component.
Stradis Healthcare is recalling Hand Packs containing Devon Light Gloves due to a manufacturer recall of the glove component by Medtronic.
Stradis Healthcare is recalling Plastic Packs containing Devon Light Gloves because the manufacturer, Medtronic, recalled the glove component.
Allergan is recalling 9 units of expired Natrelle 410cc Re-Sterilizable Breast Implant Sizers because they were shipped to the user level.
Stradis Healthcare is recalling surgical convenience kits because they contain Devon Light Gloves that are subject to a separate recall by Medtronic.
Stradis Healthcare is recalling Vaginal Rejuvenation Packs because they contain a Devon Light Glove component that Medtronic is recalling.
Stradis Healthcare is recalling Knee Arthro Packs because they contain a Devon Light Glove component that Medtronic is recalling.
Stradis Healthcare is recalling Custom Packs containing Devon Light Gloves due to a manufacturer recall of the glove component by Medtronic.
Stradis Healthcare is recalling Glaucoma Packs because they contain Devon Light Gloves that are subject to a separate recall by Medtronic.
Stradis Healthcare is recalling Head & Neck Packs containing Devon Light Gloves due to a manufacturer recall of the glove component.
Stradis Healthcare is recalling DND Packs containing Devon Light Gloves because the glove manufacturer, Medtronic, is recalling the component.
Stradis Healthcare is recalling Suction Packs containing Devon Light Gloves because the manufacturer, Medtronic, recalled the glove component.
Stradis Healthcare is recalling Vasc Custom Kits because they contain Devon Light Gloves, which are being recalled by the manufacturer Medtronic.
Stradis Healthcare is recalling Vein & Vascular Packs because they contain a Devon Light Glove component that is being recalled by its manufacturer, Medtronic.
Stradis Healthcare is recalling Standard Packs containing Devon Light Gloves because the glove component was recalled by Medtronic.
American Health Packaging is recalling 838 cartons of Azithromycin 600mg tablets because the firm did not adequately investigate customer complaints.
Stradis Healthcare is recalling Skin and Vein Packs because they contain Devon Light Gloves that Medtronic is recalling.
Stradis Healthcare is recalling Phleb Packs and Laser Phleb Packs because they contain Devon Light Gloves that are subject to a separate manufacturer recall.
Apotex Inc. is recalling 23,076 bottles of Losartan potassium tablets 50 mg because the product may not meet blend uniformity specifications.
BioComp Pharma is recalling 40,000 sachets of Thera-Gesic Pain Relieving Creme because the active ingredients menthol and methyl salicylate are below specification.
Stradis Healthcare is recalling 15 endovenous kits because they contain Devon Light Gloves, a component recalled by Medtronic.
Volcano Corp is recalling 227 intravascular ultrasound systems due to a limitation that may affect Fraction Flow Reserve calculations when connected to specific Philips monitors.
Stradis Healthcare is recalling Mississippi Packs containing Devon Light Gloves due to a manufacturer recall of the glove component.
Stradis Healthcare is recalling Face Neck Packs containing Devon Light Gloves due to a manufacturer recall of the glove component.
Apotex Inc. is recalling Losartan potassium tablets 100 mg because they may not meet blend uniformity specifications. The recall covers 23,178 bottles distributed nationwide, in Hawaii, and Puerto Rico.
Stradis Healthcare is recalling Minor Pack and Minor Pack II surgical kits because they contain a recalled Devon Light Glove component.
Stradis Healthcare is recalling Podiatry Packs because they contain Devon Light Gloves that are subject to a separate recall by Medtronic.
American Health Packaging is recalling 97,837 cartons of Famotidine tablets 20mg due to CGMP deviations involving inadequate investigation of customer complaints.
American Health Packaging is recalling Amlodipine besylate tablets 10 mg due to current Good Manufacturing Practice (CGMP) deviations involving inadequate investigation of customer complaints.
American Health Packaging is recalling 13,532 cartons of Lisinopril 10mg tablets because the firm did not adequately investigate customer complaints.
Volcano Corp is recalling 227 Intravascular Ultrasound Imaging and Pressure Systems due to a limitation in interoperability with the Philips Xper Flex Cardia system that may impact Fraction Flow Reserve calculations.
American Health Packaging is recalling Amlodipine besylate tablets 5mg due to CGMP deviations involving inadequate investigation of customer complaints.
Stradis Healthcare is recalling Lima Pack surgical kits because they contain a Devon Light Glove component that Medtronic is recalling.
American Health Packaging is recalling 5,591 cartons of Lisinopril 20mg tablets nationwide because the firm did not adequately investigate customer complaints.
American Health Packaging is recalling specific lots of Azithromycin tablets because the firm did not adequately investigate customer complaints.
Apotex Inc. is recalling Losartan potassium tablets 25 mg because they may not meet blend uniformity specifications. The recall covers 45,708 bottles distributed nationwide, in Hawaii, and Puerto Rico.
American Health Packaging is recalling Zonisamide capsules due to current good manufacturing practice deviations involving inadequate investigation of customer complaints.
American Health Packaging is recalling 1,896 cartons of Amlodipine besylate tablets 2.5mg due to inadequate investigation of customer complaints.
Mylan Pharmaceuticals is recalling 1,068 bottles of Capecitabine Tablets, 500 mg, because the product failed to meet dissolution specifications.
Hospira Inc. is recalling 106,900 vials of Magnesium Sulfate Injection, USP, 50% because 12-month stability testing failed pH specifications.
Stradis Healthcare is recalling Orthopedic Split Drape Packs because they contain a Devon Light Glove component recalled by Medtronic.
World of Coca-Cola is recalling DASANI Purified Water because some bottles may contain linear pieces of plastic from the production process.
Integra LifeSciences is voluntarily recalling 123 Tuohy needles because they were incorrectly labeled as 18 gauge, 3.5 inch instead of 20 gauge, 5 inch.
Volk Optical Inc is recalling 78 units of the Lombart 90D Clear lens due to an incorrect lot number engraved on the aluminum ring.
Bard Access Systems is recalling PowerPICC Solo Catheter Kits because they have incorrect expiration dates on the primary labeling.
Abrams Royal Pharmacy II is recalling CORTISOL-MC 10mg capsules because they failed uniformity of dosage unit specifications.
Bard Access Systems is recalling PowerPICC Solo Catheter Kits because the primary labels contain incorrect expiration dates.
Bard Access Systems is recalling PowerPICC Solo Catheter Kits because the primary labels contain incorrect expiration dates.
Bard Access Systems is recalling PowerPICC Solo Catheter Kits because the primary labels display incorrect expiration dates.
Emcara is recalling specific Pressure Relief Devices (PRDs) that may fail to vent pressure, potentially causing CNG tank explosions, fire, and injury.
Agility Fuel Systems is recalling certain compressed natural gas (CNG) fuel systems because pressure relief devices may fail to vent pressure, increasing the risk of tank explosion, fire, and injury.
Kia is recalling 2016 Sorento vehicles because the front passenger seat belt buckle may prevent fastening, increasing injury risk in a crash.
Hercules Tire & Rubber Company is recalling approximately 90,000 All Trac A/T tires because the tread may separate, increasing the risk of a vehicle crash.
Starcraft is recalling 800 commercial buses from 2002-2007 because they may exceed their weight rating when loaded, risking poor handling or tire failure.
Continental is recalling specific ContiProContact tires due to a risk of tread separation, which could lead to sudden air loss and a vehicle crash.
Barber Foods is recalling approximately 1.7 million pounds of frozen, raw stuffed chicken products that may be contaminated with Salmonella Enteritidis.
Chrysler is recalling 2008-2010 Dodge Challengers because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.
Wilson Trailer Company is recalling 2006-2015 Grain trailers because welds on the kingpin assembly may fail, potentially causing the trailer to detach from the tractor.
KTM is recalling 640 model year 2014 1290 Super Duke R motorcycles because fuel may leak from the gas tank, increasing fire risk.
Autocar is recalling 1,042 model year 2015-2016 Xpeditor vehicles because the defrost mode door actuators in the HVAC units may overheat, increasing the risk of a fire.
General Motors is recalling specific 2014-2015 Chevrolet Cruze and 2015 Chevrolet Volt vehicles because the inner tie rod may not be tightened correctly, which could cause the tie rod to separate from the steering gear.
Gourmet Culinary Solutions is recalling approximately 495 pounds of turkey sausage products that may contain pieces of a conveyor belt.
Hearth & Home Technologies is recalling about 2,500 indoor gas fireplaces because the back of the firebox can bow out, posing a fire hazard.
Jake's Fireworks is recalling YoYo Sparklers because they burn rapidly down the stick, posing a burn hazard to users' hands.
Epoca International is recalling about 113,000 glass whistling kettles because the bottom can break when heated, posing laceration and burn risks.
Black Diamond is recalling JetForce avalanche airbag packs because the motor may fail to deploy, increasing injury risk.
Öhlins USA is recalling about 50 RXF 48 front forks for motocross bikes because they can break or detach, posing a crash hazard.
Hearth & Home Technologies is recalling about 2,000 Quadra-Fire Mt. Vernon E2 pellet stoves and inserts because fuel backup can cause glass to break, posing a laceration hazard.
Snoqualmie Gourmet Ice Cream is recalling 10% Soft-Serve Vanilla Ice Cream Mix because finished product tested positive for Listeria monocytogenes.
Snoqualmie Gourmet Ice Cream is recalling Orange Sorbet due to potential Listeria monocytogenes contamination. The product was distributed nationwide in 1.5 and 3 gallon tubs.
Snoqualmie Gourmet Ice Cream is recalling Lemon Meyer Sorbet due to potential Listeria monocytogenes contamination. The product was sold nationwide in 1.5 and 3-gallon tubs.
Snoqualmie Gourmet Ice Cream is recalling Chocolate High Protein Shake Ice Cream Mix due to the presence of Listeria monocytogenes.
Snoqualmie Gourmet Ice Cream is recalling Lemoncello-Mint Gelato due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Snoqualmie Gourmet Ice Cream is recalling Lemon Sorbet with Lemon Swirl due to potential Listeria monocytogenes contamination.
Snoqualmie Gourmet Ice Cream is recalling Chocolate Chip Cookie Dough Custard due to potential Listeria monocytogenes contamination.
Snoqualmie Gourmet Ice Cream is recalling Raspberry Pomegranate Sorbet due to potential Listeria monocytogenes contamination.
Snoqualmie Gourmet Ice Cream is recalling four sorbet products due to potential Listeria monocytogenes contamination. The products were distributed nationwide.
Snoqualmie Gourmet Ice Cream is recalling Blueberry Ginger Sorbet due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Snoqualmie Gourmet Ice Cream is recalling Coffee Gelato due to potential contamination with Listeria monocytogenes. The product was distributed nationwide.
Snoqualmie Gourmet Ice Cream is recalling 10% Soft-Serve Chocolate Ice Cream Mix due to potential Listeria monocytogenes contamination.
Snoqualmie Gourmet Ice Cream is recalling Cherry Sorbet due to potential Listeria monocytogenes contamination. The product was distributed nationwide in 3-gallon tubs.
Snoqualmie Gourmet Ice Cream is recalling Gelato Mix due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Snoqualmie Gourmet Ice Cream is recalling Cherry Vanilla Custard due to potential Listeria monocytogenes contamination.
Snoqualmie Gourmet Ice Cream is recalling Reisling Sorbet due to potential Listeria monocytogenes contamination. The product was distributed nationwide in 1.5 and 3 gallon tubs.
Snoqualmie Gourmet Ice Cream is recalling Lemon Thyme Sorbet due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Snoqualmie Gourmet Ice Cream is recalling Egg Nog products due to the potential for Listeria monocytogenes contamination.
Snoqualmie Gourmet Ice Cream is recalling Strawberry Cosmo Lemon Twist Sorbet due to potential Listeria monocytogenes contamination.
Snoqualmie Gourmet Ice Cream is recalling Pear Sorbet due to potential Listeria monocytogenes contamination. The product was distributed nationwide in 3-gallon tubs.
Snoqualmie Gourmet Ice Cream is recalling Honey Cinnamon Custard due to the presence of Listeria monocytogenes. The product is sold in 1.5 and 3 gallon plastic tubs.
Snoqualmie Gourmet Ice Cream is recalling Pumpkin Custard due to the presence of Listeria monocytogenes. The product was distributed nationwide in 1.5 and 3 gallon tubs.
Snoqualmie Gourmet Ice Cream is recalling Double Chocolate Custard due to potential Listeria monocytogenes contamination.
Snoqualmie Gourmet Ice Cream is recalling Honey Cinnamon Custard due to potential Listeria monocytogenes contamination.
Snoqualmie Gourmet Ice Cream is recalling Mango Pistachio Gelato due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Snoqualmie Gourmet Ice Cream is recalling Chocolate Custard with Espresso Chips due to potential Listeria monocytogenes contamination.
Snoqualmie Gourmet Ice Cream is recalling Apricot Sorbet due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Snoqualmie Gourmet Ice Cream is recalling Creme Fraiche Gelato due to potential Listeria monocytogenes contamination. The product was distributed nationwide in 16 oz pints.
Snoqualmie Gourmet Ice Cream is recalling Vanilla High Protein Shake Ice Cream Mix due to the presence of Listeria monocytogenes.
Snoqualmie Gourmet Ice Cream is recalling Lemon Lime Sorbet due to potential Listeria monocytogenes contamination. The product was distributed nationwide in pints and gallon tubs.
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