Archive
1,402 recalls were announced in December 2013.
Of the 1,402 recalls this month scored against our rubric, 25% are Critical, 42% are Severe.
Which agencies issued them
National Enzyme Co is recalling ZoiVi Digestive Formula powder because it may contain chloramphenicol above 0.3 ppb.
National Enzyme Co is recalling ProSol Professional Solutions Fiber Digestion Enzyme Supplement because it may contain chloramphenicol above the permitted limit.
National Enzyme Co is recalling BioSan Enzyme Blend 3 O capsules because the raw material may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling Applied Health blue-green algae supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling specific lots of Gluten & Dairy Digest enzyme supplements because they may contain chloramphenicol above 0.3 ppb.
Nature's Way is voluntarily recalling Alive No Iron tablets because the raw material supplier reported that enzymes in the blend may contain the antibiotic chloramphenicol.
LSG Food World Inc. is recalling Noodles House Home Style Noodles because the product contains an unapproved color and an undeclared food additive.
Karl Storz Endoscopy America is recalling 141 flexible broncho fiberscopes because the suction channel material is not listed for STERRAD sterilization systems.
National Enzyme Co is recalling bulk dietary supplement capsules because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling Bulk B983 Vitamin Shoppe Advanced powder because it may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling PerformanceZyme dietary supplements because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.
Balajee Trade Link LLC is recalling DRUK Orange Squash because FDA analysis found it contains undeclared sunset yellow FCF.
Schwabe North America is voluntarily recalling Nature's Way Alive Once Daily Women's Ultra Potency tablets because the raw material supplier reported that enzymes in the blend may contain the antibiotic chloramphenicol.
National Enzyme Co is recalling Heryben and Bulk C269 dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling Cellulase Cellulolytic Enzymes because the raw material may contain chloramphenicol levels exceeding 0.3 ppb.
Airgas Medical Services is recalling 264 carbon dioxide cylinders because one was incorrectly labeled as a gas withdrawal cylinder instead of a liquid withdrawal cylinder.
Schwabe North America is voluntarily recalling Nature's Way Alive Whole Food Energizer Multivitamin because raw material enzymes may contain the antibiotic chloramphenicol.
National Enzyme Co is recalling 1,751 bottles of Healthy Digest dietary supplements because they may contain chloramphenicol above 0.3 ppb.
Schwabe North America is voluntarily recalling Nature's Way Alive Whole Food Energizer tablets because raw material enzymes may contain the antibiotic chloramphenicol.
National Enzyme Co is recalling bulk enzyme powder that may contain chloramphenicol above permitted limits. The product is distributed domestically and internationally.
Instrumentation Laboratory is recalling 8,0319 kits of HemosIL Normal Control 1 UNASSAYED because the product lacks FDA 510(k) approval.
National Enzyme Co is recalling Bulk C542 Vitakost Low Carb Diet because the raw material may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling bulk Digest Platinum capsules because they may contain chloramphenicol above 0.3 ppb.
Qualigen Inc is recalling 17 units of the FastPack Free T4 Immunoassay because a manufacturing defect may cause lower than expected test results.
Stryker Neurovascular is recalling Excelsior SL-10 microcatheters because they were shipped with use-by dates exceeding available shelf-life data.
National Enzyme Co is recalling Multi Plant Enzyme Tablets because a raw material may contain chloramphenicol above 0.3 ppb.
Stryker Neurovascular is recalling Excelsior microcatheters because they were shipped with use-by dates exceeding available shelf-life data.
Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates exceeding available shelf-life data.
Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with use-by dates exceeding available shelf-life data.
Biomet, Inc. is recalling 21 CurvTek Eye Needles because the inner label incorrectly identifies the product size and reference number.
National Enzyme Co is recalling bulk dietary supplement powders that may contain chloramphenicol levels exceeding 0.3 ppb.
A&C US Trading LLC is recalling Lam Sheng Kee Haw Flakes because the product contains unapproved food coloring. The recall affects 600 cartons distributed in New York.
National Enzyme Co is recalling 9326 Kirkman Bacterial Bio 6 dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling B911 Kirkman Max Spectrum E dietary supplements because they may contain chloramphenicol above 0.3 ppb.
National Enzyme Co is recalling specific lots of DigestBasicK capsules because they may contain chloramphenicol above 0.3 ppb.
CooperVision is recalling specific lots of ClearSight Toric 1 day contact lenses because the outer cartons display incorrect expiration dates, though the inner blisters are correct.
SpineFrontier, Inc. is recalling 35 PedFuse Reset pedicle screws because one unit was found assembled with the wrong size screw. The recall covers devices distributed to Virginia and Texas.
Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates that exceed available shelf-life data.
National Enzyme Co is recalling specific dietary supplements because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.
Microgenics Corp. is recalling CEDIA Tobramycin II Assay (Lot 60169764) due to a calibration stability problem identified through two customer complaints.
National Enzyme Co is recalling bulk dietary supplement capsules because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.
Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with use-by dates exceeding available shelf-life data.
National Enzyme Co is recalling bulk TriEnz powder because it may contain chloramphenicol levels exceeding 0.3 ppb.
Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates exceeding available shelf-life data.
Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with use-by dates exceeding available shelf-life data.
Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates exceeding available shelf-life data.
Stryker Neurovascular is recalling certain microcatheters and coils because they were shipped with use-by dates exceeding available shelf-life data.
Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates that exceed available shelf-life data.
Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with use-by dates exceeding available shelf-life data.
Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates that exceed available shelf-life data.
National Enzyme Co is recalling specific dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling bulk enzyme powder that may contain chloramphenicol above the permitted limit.
Nature's Way is voluntarily recalling NL C 24/7 Bulk Caps because raw material enzymes may contain the antibiotic chloramphenicol.
LSG Food World Inc. is recalling Noodles House Home Style Noodles due to the use of an unapproved color and an undeclared food additive.
National Enzyme Co is recalling MaxEnzComp dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.
Tween Brands is recalling 42,570 units of Green Apple hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of 20%.
National Enzyme Co is recalling specific dietary supplement bottles because they may contain chloramphenicol levels exceeding 0.3 ppb.
Tween Brands Inc is recalling Share a Smile Mixed Berry hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.
National Enzyme Co is recalling Wellzymes enzyme supplements because a raw material may contain chloramphenicol above the 0.3 ppb limit.
National Enzyme Co is recalling bulk digestive supplements that may contain chloramphenicol above 0.3 ppb. The product was distributed domestically and internationally.
National Enzyme Co is recalling bulk B807 True Botanica Digestive dietary supplements because the raw material may contain chloramphenicol levels exceeding 0.3 ppb.
Beckman Coulter is recalling Access Immunoassay Reaction Vessels due to intermittent wash carousel motion errors affecting specific lots.
Schwabe North America is voluntarily recalling Nature's Way Alive Once Daily MultiVitamin Ultra Potency tablets because raw material enzymes may contain the antibiotic chloramphenicol.
National Enzyme Co is recalling bulk enzyme powder that may contain chloramphenicol above 0.3 ppb.
National Enzyme Co is recalling specific dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling Healthy Reflections Colon Health Support supplements because a raw material may contain chloramphenicol above 0.3 ppb.
Remel Inc is recalling Oxoid Ciprofloxacin test discs because boxes labeled CIP5 may contain AMP5 cartridges.
Tween Brands Inc is recalling 4,692 bottles of BFF's are COOL! Justice Cherry Scent Anti Bac because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.
Tween Brands Inc is recalling 27,590 bottles of Lemon Anti Bac Justice because the label incorrectly states the ethyl alcohol content is 62% instead of 20%.
Tween Brands Inc is recalling 20,167 bottles of 'I MUSTACHE YOU TO BE MY BFF' hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.
Tween Brands Inc is recalling 47,051 bottles of 'I love my BFF Justice' Watermelon anti-bac hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% when it is actually 20%.
Tween Brands Inc is recalling 15,931 bottles of Grape Scented Anti-Bac because the label incorrectly states the ethyl alcohol content is 62% instead of 20%.
Fresenius Kabi USA is recalling folic acid injection vials due to failed impurity and degradation specifications at 14 and 15 months.
Tween Brands Inc is recalling 47,343 bottles of hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.
Tween Brands Inc is recalling 23,231 bottles of Peach anti-bac hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.
Tween Brands Inc is recalling 21,201 bottles of I love sleep overs Justice, Grape anti bac hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of 20%.
Tween Brands Inc is recalling 65,332 bottles of Justice Chocolate anti-bacterial hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of 20%.
Nephros Inc. is recalling SafeShower and SafeSpout water filters because promotional materials marketed them as medical devices.
Nephros Inc is recalling brochures for its Dual Stage Ultra Filter because the materials promoted the product as a medical device.
Tween Brands Inc is recalling 16,471 bottles of I Love Bacon Justice hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.
Tween Brands Inc is recalling 9,558 bottles of Girls Rock Justice hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of 20%.
Tween Brands Inc is recalling 86,701 bottles of Believe in Yourself Strawberry Anti bac Justice hand sanitizer because the label incorrectly states the ethyl alcohol content.
Tween Brands Inc is recalling 25,078 bottles of Shine from Within Blueberry Anti-Bac Justice because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.
Tween Brands Inc is recalling 58,054 bottles of LIFE IS SWEET! Justice hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.
Tween Brands Inc is recalling 18,492 bottles of Grapefruit anti bac Justice because the label incorrectly states the ethyl alcohol content is 62% instead of 20%.
Blue Bird is recalling 2014-2015 All American and Vision school buses because a parking brake component may fracture, causing the brake to release unexpectedly.
Meritor is recalling specific remanufactured trailer axles where misaligned parts could cause wheel separation and increase crash risk.
Nissan is recalling 2014 Titan King Cab and Crew Cab trucks because the tire and loading information label overstates the vehicle's maximum load and passenger capacity.
Airstream is recalling Fiamma-brand bicycle racks that may partially block the rear emergency exit of trailers when loaded.
Cargo South is recalling 2006-2013 enclosed utility trailers because a door lock defect may jam the deadbolt, potentially trapping occupants inside.
Landscape Structures is recalling Oodle Swings because the seat is suspended too close to the ground, posing a leg injury risk to children.
Mack is recalling 2014 Pinnacle CXU tractors because an incorrectly wired over-speed protection system may fail to shut down the engine, risking fire.
General Motors is recalling 2014 Chevrolet Silverados and GMC Sierras because incorrect transmission software may fail to display first gear, increasing crash risk.
Daimler Trucks North America is recalling 45 school buses because an incorrect speedometer calibration may display a lower speed than the vehicle is actually traveling.
Daimler Trucks North America is recalling 2014 Freightliner chassis because an incorrect speedometer calibration may display a lower speed than actual, increasing crash risk.
Starcraft is recalling 50 model year 2014 Comet recreational vehicles because certification labels incorrectly identify tire load ranges, potentially leading to unsafe tire replacements.
Riverside is recalling 2006-2014 travel trailers with Fastec door locks that may jam, potentially trapping occupants inside the vehicle.
Yankee Candle is recalling Pine Berry candle rings because their synthetic foliage and berries are flammable, posing a fire hazard. No injuries have been reported.
Playtex is recalling Hip Hammock infant carriers because buckles can crack or break, posing a fall hazard to children.
Nova Bus is recalling 2009-2012 LFS transit buses because a specific potting compound in DC-DC converters can conduct electricity and cause fires.
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