Archive
854 recalls were announced in March 2017.
Of the 854 recalls this month scored against our rubric, 11% are Critical, 25% are Severe.
Which agencies issued them
Tiffin is recalling 2011-2016 Allegro Open Road motorhomes because the tow hitch may detach under heavy loading or hard braking, increasing crash risk.
Hino is recalling 2013-2017 XFC hybrid trucks because the clutch drum spline may wear out, causing the vehicle to lose power and increasing crash risk.
Chrysler is recalling 2016-2017 Ram 1500 trucks because a differential pin screw may loosen, potentially causing the differential to break or lock up and increasing crash risk.
Blue Bird is recalling 2017-2018 Vision transit buses because a propane fuel control valve solenoid may short circuit, causing the engine to shut off while driving.
Haibike is recalling specific XDURO electric bicycles because the front fork can rupture or break, posing a fall hazard to riders.
McNeilus is recalling 2013-2015 refuse trucks with CNG systems because flexible fuel hoses may corrode, potentially causing a leak and fire.
Wing Enterprises is recalling Little Giant ladders because locking pins can fail, posing a fall hazard. No injuries have been reported.
Blue Bird is recalling 2016 Vision and All American school buses because loose or missing nuts may allow shoulder belt D-rings to detach in a crash.
Vecaro LifeStyle is recalling about 500 self-balancing scooters because their lithium-ion batteries can overheat, smoke, catch fire, or explode.
ASTI is recalling power adapters sold with LectroFan sound machines because the casing can break, exposing metal prongs and posing an electrical shock hazard.
Iowa Mold Tooling is recalling one 2013 Refuse-Container Delivery truck because CNG fuel hoses may corrode, potentially causing a leak and fire.
Blue Bird is recalling 2017-2018 Vision school buses designed for propane because a fuel control valve solenoid may short circuit, causing the engine to shut off while driving.
Gel Spice Co. is recalling various ground turmeric products nationwide because they may contain excess levels of lead.
Oriental Packing Co., Inc. is recalling various brands of mild curry powder because product samples tested positive for lead.
Oriental Packing Co. is recalling hot and spicy curry powder products sold in Florida and New York because samples tested positive for lead.
Cedar Crest Specialties, Inc. is recalling specific sizes of Chocolate Chip Cookie Dough Ice Cream because the cookie dough may be contaminated with Listeria monocytogenes.
Cedar Crest Specialties is recalling Pirate's Bounty Ice Cream because the cookie dough used may be contaminated with Listeria monocytogenes.
Oriental Packing Co. is recalling Ocho Rios Mild Jerk Curry Seasoning because product samples and the ground turmeric ingredient tested positive for lead.
Sea Port Products Corp is recalling frozen raw bay scallops due to potential contamination with hepatitis A virus. The product was distributed in California, Hawaii, and Nevada.
Synergy Rx is recalling Erythromycin 2% in CeraVe Cream and Erythromycin 3% / Retinoic Acid 0.05% due to lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Kojic Acid 8%/Azelaic Acid 15% Cream because it lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling specific prescription topical gels and creams because they may lack assurance of sterility and have CGMP deviations.
Krispy Kreme Doughnut Corporation is recalling Choc Iced Kreme Filled doughnuts because they may contain metal pieces. The products were distributed in Delaware, Maryland, North Carolina, and Virginia.
Synergy Rx is recalling Clarifying Cream due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling HI-LITE Cream because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Malek's Magic Plus prescription cream because it lacks assurance of sterility and has CGMP deviations.
Box Mill Farm is recalling pasteurized apple cider in gallon and half-gallon containers due to inadequate pasteurization. The product was distributed in Massachusetts.
Synergy Rx is recalling all lots of Purified Water due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Fluorouracil creams due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Supreme Cream due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Brightening Cream due to a lack of assurance of sterility and CGMP deviations. The product is distributed nationwide.
Synergy Rx is recalling TCA Peel Solutions in all strengths due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling 1,809 vials of Human Chorionic Gonadotropin (HCG) because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Gentle Bleaching Cream because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Bleaching Cream products due to a lack of assurance of sterility and CGMP deviations.
Del Mar Reynolds Medical is recalling Arkon Anesthesia Delivery Systems because the power supply can fail without triggering normal battery alarms.
Synergy Rx is recalling all lots of HCG products nationwide due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling all strengths of Glycolic Acid Solution because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Cantharidin 0.7% Solution and Cantharidan/Podophyllum Solution due to lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Fluorouracil creams because of a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Gentle Supreme Bleaching Cream because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling ACNE SOLUTION, a prescription topical medication, due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Tri-Bleaching Cream because it lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling all lots of CLEAR 2 (Benzoyl Peroxide 2.5%, Clindamycin 1.2%) because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Hydroquinone Solution in all strengths due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Lactic Acid Solution in all strengths due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling various lidocaine cream and ointment products nationwide due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling TRI-BLEACHING CREAM HQ because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling VI PEEL chemical peel products nationwide due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling specific clindamycin and tretinoin products due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Rosacea Cream because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling QUAD PEEL chemical peels nationwide due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling all lots of Ketoconazole 2%/Hydrocortisone 1.5% Cream because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Vitamin K Oxide 5% because it lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Diclofenac Lip Balm products because they may not be sterile. The recall covers all lots distributed nationwide.
Synergy Rx is recalling Human Chorionic Gonadotropin tablets because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Azelaic Acid 15% Cream because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Sulfur 5% Cream due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Hydrocortisone 2.5% with Aloe Vera Cream because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Custom Lightening/Brightening Cream due to lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Calming Cream (Hydrocortisone 2.5%) because the product lacks assurance of sterility and has CGMP deviations.
Kingsway Trading Inc is recalling Xanthium & Siler Combo (Bi Yan Pian) dietary supplements because they contain Ephedrae Herba (ma huang), a banned ephedra alkaloid.
Synergy Rx is recalling HCG and HCG with resveratrol tablets nationwide due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Urea 40% Cream because it may not be sterile and has CGMP deviations.
Synergy Rx is recalling Sulfacetamide 10%/Hydrocortisone 1% Cream due to lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Quad Bleaching Cream because it lacks assurance of sterility and has CGMP deviations.
J M Exotic Foods Inc is recalling specific lots of ground turmeric because a supplier sample tested with elevated lead levels. The product was distributed in Georgia and Alabama.
Newmar is recalling 595 motorhomes because front suspension ball joints can loosen and separate, potentially causing a loss of steering control.
Synergy Rx is recalling various retinoic acid products due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Betamethasone 0.25% cream because it may not be sterile. The recall covers all lots distributed nationwide.
Bee International is recalling Plastic Heart Tubes with Chocolate Lentils because they may contain undeclared milk protein.
Synergy Rx is recalling Enhanced Retin Anti-Wrinkle Cream products due to a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Minoxidil and Minoxidil/Retinoic Acid products nationwide due to a lack of assurance of sterility and CGMP deviations.
Oriental Packing Co. is recalling specific lots of jerk curry powder because product samples and ingredients tested positive for lead.
Cedar Crest Specialties is recalling specific 3-gallon containers of Monster Cookie Dough Ice Cream because the cookie dough may be contaminated with Listeria monocytogenes.
Synergy Rx is recalling Supreme Bleaching Cream due to a lack of assurance of sterility and CGMP deviations.
Teva Pharmaceuticals is recalling specific lots of Buprenorphine and Naloxone Sublingual Tablets because they failed impurity and degradation specifications.
Synergy Rx is recalling Benzoyl Peroxide 5% Clindamycin 1.2% due to lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling Clobetasol 0.05% products because the FDA identified a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling all lots of Tacrolimus 0.1% Ointment and Tacrolimus 0.1%/Ketoconazole 2% due to lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling DUO Cream because the product lacks assurance of sterility and has CGMP deviations. The recall covers all lots distributed nationwide.
Synergy Rx is recalling LP Cream (Lidocaine 15%/Prilocaine 5%) because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling LTP (Lidocaine 10%, Tetracaine 2%, Phenylephrine 0.5%) ophthalmic solution nationwide due to lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling all lots of CLEAR (Benzoyl Peroxide 3.75%, Clindamycin 1.2% Gel) due to a lack of assurance of sterility and CGMP deviations.
Isomeric Pharmacy Solution is recalling 6,999 vials of Triamcinolone 40 mg/mL injection due to Current Good Manufacturing Practice (CGMP) deviations.
Synergy Rx is recalling MALEK'S MAGIC prescription cream because it lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Tri-Bleaching Cream because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Intimate Bleaching Cream because the product lacks assurance of sterility and has CGMP deviations.
Synergy Rx is recalling Hydroquinone Cream in all strengths due to a lack of assurance of sterility and CGMP deviations.
Kiscomedica S.A. is recalling 13 units of the L-Varlock Cage/Trial Implant Holder because the tip holder broke during use.
Nachman's Native Seafood is recalling Smoked Fish spread in various sizes due to undeclared wheat in the soy sauce ingredient.
CareFusion is recalling 12,850 MaxGuard Extension Sets because the 0.2 micron filter may leak. These medical devices are used to administer fluids to patients.
Maquet Cardiovascular is recalling 4,283 VASOVIEW HEMOPRO VH-3500 units due to reports of intermittent or no power.
Krispy Kreme Doughnut Corporation is recalling 717 units of Chocolate Iced Sprinkle Theme donuts because they may contain metal pieces.
Del Monte Fresh Produce is recalling Choice Farms Portabella Mushroom trays due to possible Listeria monocytogenes contamination.
Medtronic is recalling SharkCore LG Fine Needle Biopsy Systems because the handle may break during use.
Sweets & Desserts, Inc. is recalling 384 units of Cheesecake Cherry in Puerto Rico due to undeclared milk and Red #40 food color.
Merge Healthcare is recalling iConnect Enterprise Archive software versions 5.30.0 through 9.4.3 and V11.0 because routing exceptions may delay diagnosis or treatment.
Synergy Rx is recalling salicylic acid and 5-FU prescription products due to lack of assurance of sterility and CGMP deviations.
Sweets & Desserts, Inc. is recalling Cheesecake Fresa (Strawberry) in Puerto Rico due to undeclared milk and Red #40 food color.
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