Archive
494 recalls were announced in January 2018.
Of the 494 recalls this month scored against our rubric, 8% are Critical, 24% are Severe.
Which agencies issued them
KRS Global Biotechnology is recalling 1,203 vials of Human Chorionic Gonadotropin due to incorrect or missing lot and expiration dates.
KRS Global Biotechnology is recalling Chloramphenicol 50 mg/Sulfamethoxazole 50 mg/Amphotericin-B 5 mg capsules because the Beyond Use Date exceeds the expiration date of at least one ingredient.
Amendia, Inc. is recalling 41 Mac Pin Non-Cannulated Screws because the packaging incorrectly lists the length as 460 mm, while the actual length is 60 mm.
McCain Foods USA is recalling Publix brand Southern Style Diced Hash Brown Potatoes after consumer complaints of foreign material in the product.
Saputo Cheese USA Inc. is recalling Light String Cheese sold under multiple brands due to an off odor and off taste.
Nutricia North America is recalling SHS Wel-Plan Wheat and Corn Starch Baking Mix due to low-level Klebsiella pneumoniae contamination. The recall is precautionary as the product is intended to be cooked.
KRS Global Biotechnology is recalling 4,530 jars of Benzocaine 20%, Lidocaine 6%, Tetracaine 4% Cream because the Beyond Use Date exceeds the expiration date of at least one ingredient.
KRS Global Biotechnology is recalling 122 vials of QUADMIX #17 because the product's beyond-use date exceeds the expiration date of at least one ingredient.
KRS Global Biotechnology is recalling 1,009 vials of Hydroxocobalamin 0.5 mg/mL because the Beyond Use Date exceeds the expiration date of at least one ingredient.
KRS Global Biotechnology is recalling 81 droptainers of a multi-dose ophthalmic solution because the Beyond Use Date exceeds the expiration date of at least one ingredient.
KRS Global Biotechnology is recalling 963 bags of Oxytocin 30 Units IV solution because the Beyond Use Date exceeds the expiration date of at least one ingredient.
KRS Global Biotechnology is recalling 5,786 vials of Vitamin 10 B Lyophilized Vial due to incorrect or missing lot and expiration dates.
KRS Global Biotechnology is recalling 7-Keto DHEA 25mg capsules because the Beyond Use Date exceeds the expiration date of at least one ingredient.
KRS Global Biotechnology is recalling 6,414 vials of Human Chorionic Gonadotropin because the Beyond Use Date exceeds the expiration date of at least one ingredient.
KRS Global Biotechnology is recalling 126 vials of QUADMIX #16 because the Beyond Use Date exceeds the expiration date of at least one ingredient.
Dr. Reddy's is recalling 1,051 vials of Docetaxel Injection USP due to defects in the vial seals that may allow the stopper to detach.
Brainlab AG is recalling DrapeLink Adapters because a supplier error caused some units to not meet specifications.
Spice Chain Corporation is recalling Paprika HUN Kalosca 12/5o after receiving consumer complaints of finding beetles in retail containers.
KRS Global Biotechnology is recalling Savinase 100 mcg/mL Topical Solution because the product's beyond-use date exceeds the expiration date of at least one ingredient.
Prinston Pharmaceutical Inc. is recalling 21,987 bottles of Valsartan 160 mg tablets because customer complaints confirmed the tablets were thicker and heavier than specifications.
Bush Brothers & Co is recalling Bush's Best Homestyle Tangy Sauce Baked Beans because some cans were found to be swollen.
Spice Chain Corporation is recalling Paprika Sweet American Garden after consumer complaints of finding beetles in retail containers.
Spice Chain Corporation is recalling Paprika Hun Budapest 12/5oz after consumers reported finding beetles in retail containers.
KRS Global Biotechnology is recalling 2,239 vials of Human Chorionic Gonadotropin because the Beyond Use Date exceeds the expiration date of at least one ingredient.
KRS Global Biotechnology is recalling 300 jars of Bi-Est Cream because the Beyond Use Date exceeds the expiration date of at least one ingredient.
KRS Global Biotechnology is recalling 696 vials of Methylene Blue (PF) 10 mg/mL Injectable due to incorrect or missing lot and expiration dates.
KRS Global Biotechnology is recalling 3,612 vials of Vitamin 9 A/B Lyophilized Vials because the Beyond Use Date exceeds the expiration date of at least one ingredient.
KRS Global Biotechnology is recalling 15,700 capsules of Anastrozole 0.5 mg due to incorrect or missing lot and expiration dates.
KRS Global Biotechnology is recalling Liothyronine SR 20 mcg capsules because the Beyond Use Date exceeds the expiration date of at least one ingredient.
KRS Global Biotechnology is recalling 2,535 vials of Nicotinamide Adenine Dinucleotide 500 mg because the Beyond Use Date exceeds the expiration date of at least one ingredient.
KRS Global Biotechnology is recalling 30 jars of Hydroquinone 8%/Tretinoin 0.1% Topical Ointment because the Beyond Use Date exceeds the expiration date of at least one ingredient.
KRS Global Biotechnology is recalling 479 vials of Vitamin 9 Lyophilized Vial due to incorrect or missing lot and expiration dates.
KRS Global Biotechnology is recalling 300 jars of Estriol 0.1% Cream because the product's beyond-use date exceeds that of at least one ingredient.
KRS Global Biotechnology is recalling 597 vials of Sermorelin and related peptides because the Beyond Use Date exceeds the expiration of at least one ingredient.
KRS Global Biotechnology is recalling 2,274 vials of Human Chorionic Gonadotropin 20,000 iu due to incorrect or missing lot and expiration dates.
KRS Global Biotechnology is recalling 2,239 Human Chorionic Gonadotropin tablets because the expiration date exceeds the shelf life of an ingredient.
SCA Pharmaceuticals is recalling 1,248 syringes of Ephedrine sulfate 5 mg/mL because the product labels were missing the lot number and beyond-use date.
KRS Global Biotechnology is recalling 94 vials of Trimix #23F because the product's expiration date exceeds the expiration date of at least one ingredient.
KRS Global Biotechnology is recalling 20 jars of Chloramphenicol and Amphotericin Otic Powder because the Beyond Use Date exceeds the expiration of at least one ingredient.
KRS Global Biotechnology is recalling 7-Keto DHEA 100 mg capsules because the product's expiration date exceeds the expiration date of at least one ingredient.
Akorn Inc is recalling 4,885 bottles of Gabapentin Oral Solution because the product was released with an unapproved active ingredient manufacturer.
Sanofi-Aventis is recalling Enoxaparin Sodium injections because a single syringe with a different strength was found in a carton labeled 120 mg/0.8 mL.
Mazda is recalling 2,205 model year 2006 B-Series trucks because the driver-side air bag inflator may explode upon deployment, posing a risk of serious injury or death.
Dorman is recalling specific A/C Bypass Pulley Brackets that may crack under certain loading conditions. A failure could cause the vehicle to lose power steering assist, increasing the risk of a crash.
Mazda is recalling 2,205 model year 2006 B-Series trucks because the front air bag inflators may explode during deployment, posing a risk of serious injury or death.
Liberty is recalling 2018 Little Guy Max trailers because a cracked touch pad on the power tongue jack may allow water entry, causing the jack to operate unintentionally.
Indian Motorcycle is recalling 2015-2017 Roadmaster models because water in the trunk wiring harness may cause the brake light to stay on, increasing crash risk.
Ford is recalling 2018 Expedition and Lincoln Navigator vehicles because second-row power window modules may fail to reverse if an object is pinched, increasing injury risk.
Fujifilm is recalling power adapter wall plugs sold with certain digital cameras because they can crack or break, exposing live electrical contacts and posing a shock hazard.
Foretravel is recalling 2004-2019 motorhomes because the installed fire extinguishers may clog or detach, potentially failing to work during a fire.
Elgin is recalling 2017 Crosswind street sweepers because debris may contact the exhaust system, increasing the risk of a fire.
Coldwater Creek is recalling two snow globe models because light refraction can singe or melt nearby items, posing a fire hazard.
Forest River is recalling specific 2017-2018 recreational trailers because a cracked touch pad on the power tongue jack may allow water entry, causing the jack to operate unintentionally.
Jaguar is recalling 2017-2018 F-Pace vehicles because the instrument cluster may intermittently go blank, increasing crash risk. Dealers will update the software free of charge.
Altec is recalling 2014-2017 AC40-152S cranes because the electronic Load Moment and Area Protection system may display incorrect load chart values.
Ford is recalling 33,310 2006 Ranger trucks because the driver-side air bag inflator may explode during deployment, potentially causing serious injury or death.
Altec is recalling 2017 AT Aerial Devices on Ford F-550 chassis because a circuit breaker may contact the hood, potentially causing an electrical short and fire.
Ford is recalling specific 2009-2013 vehicles because passenger air bag inflators may explode due to humidity, posing a risk of serious injury or death.
Forest River is recalling 2017-2018 Cherokee travel trailers due to a wiring defect that may increase the risk of an electrical fire.
Ford is recalling 33,310 model year 2006 Ranger trucks because the passenger-side air bag inflator may explode during deployment, potentially causing serious injury or death.
Chrysler is recalling 2018 Jeep Grand Cherokee Trackhawk vehicles because a fuel line may separate, potentially causing an engine stall, fire, or crash.
Mitsubishi Fuso is recalling 2004-2017 trucks because the installed Kidde fire extinguishers may clog or detach, potentially failing to suppress fires or causing injury.
Chrysler is recalling 2017 Pacifica vehicles with 3.6L engines because software issues may cause the engine to stall, increasing crash risk.
Pierce is recalling 2015-2016 emergency vehicles because corroded rings may cause pressure relief valves to open, reducing water pressure for firefighting.
Van-Con is recalling 2016-2018 wheelchair lift buses because the lifts may not deactivate when uneven, posing a fall risk.
Rachael's Food Corporation is recalling various smoked salmon products under the Springfield Smoked Fish and Rachael's brands because they tested positive for Listeria monocytogenes.
Rachael's Food Corporation is recalling 4 oz. sliced sides of Smoked Fish Pastrami Lox due to potential Listeria monocytogenes contamination.
Meijer Distribution is recalling Cranberry Apple Stuffing Starter due to potential Listeria monocytogenes contamination in sliced apples.
Rachael's Food Corporation is recalling Boston Salads Scallion Cream Cheese Spread and Rachael's Springfield Smoked Fish due to potential Listeria monocytogenes contamination.
Rachael's Food Corporation is recalling Springfield Smoked Whitefish Meat due to potential Listeria monocytogenes contamination.
Rachael's Food Corporation is recalling its Springfield Smoked Fish Lox Cream Cheese Spread due to potential Listeria monocytogenes contamination.
Rachael's Food Corporation is recalling Springfield Smoked Fish Smoked Whole Whitefish because it may be contaminated with Listeria monocytogenes.
Rachael's Food Corporation is recalling its Smoked Fish Strawberry Cream Cheese Spread due to potential Listeria monocytogenes contamination.
Rachael's Food Corporation is recalling Springfield Smoked Fish Belly Lox due to potential Listeria monocytogenes contamination. The product was sold nationwide.
Fresenius Kabi is recalling 203,136 syringes of Midazolam Injection that were mislabeled and actually contain Ondansetron Injection.
Rachael's Food Corporation is recalling Traditional Kippered Salmon due to potential Listeria monocytogenes contamination. The product was sold nationwide through retail and online channels.
Natures Supplement is recalling Enhanced Vegetal Vigra 200 mg capsules because FDA analysis found the product was tainted with Sildenafil and marketed without an approved NDA/ANDA.
Rachael's Food Corporation is recalling Springfield Smoked Fish Hot Smoked Salmon Steaks due to potential Listeria monocytogenes contamination.
Rachael's Food Corporation is recalling Springfield Smoked Fish Hot and Spicy Cream Cheese Spread due to potential Listeria monocytogenes contamination.
Rachael's Food Corporation is recalling Springfield Smoked Fish Smoked Bluefish because it may be contaminated with Listeria monocytogenes.
Rachael's Food Corporation is recalling Springfield Smoked Fish Smoked Sable because it may be contaminated with Listeria monocytogenes. The product was sold nationwide through retail and online channels.
Rachael's Food Corporation is recalling Springfield Smoked Fish Whitefish Salad due to potential Listeria monocytogenes contamination.
Rachael's Food Corporation is recalling specific Veggie Cream Cheese Spread products due to potential Listeria monocytogenes contamination.
Rachael's Food Corporation is recalling Springfield Smoked Chubs because the product may be contaminated with Listeria monocytogenes.
Rachael's Food Corporation is recalling Springfield Smoked Fish Chunky Whitefish Spread due to potential Listeria monocytogenes contamination.
Meijer Distribution is recalling 1,244 units of Sharable Waldorf Salad due to potential Listeria monocytogenes contamination in sliced apples.
Nissan is recalling 2009-2012 Versa vehicles because the passenger air bag inflator may explode during deployment, posing a risk of serious injury or death.
Rachael's Food Corporation is recalling Smoked Trout due to potential Listeria monocytogenes contamination. Consumers should check lot numbers and discard or return the product.
Pfizer is recalling 1,972 bottles of Zoloft 25 mg tablets because weight variations caused some tablets to be sub or super potent.
Rachael's Food Corporation is recalling its Springfield Smoked Fish Spreadable Cream Cheese Spread due to potential Listeria monocytogenes contamination.
KTM is recalling 2015-2018 1290 Super Duke R and GT motorcycles because a front brake piston may fail, increasing crash risk.
Mercedes-Benz is recalling specific 2009-2013 models because the passenger air bag inflator may explode during deployment, potentially causing serious injury or death.
AJC International, Inc. is recalling Early Dawn Whole Tilapia found to contain the antibiotic Sulfadiazine. The product was distributed in Pennsylvania.
Meijer Distribution is recalling 1,824 units of Michigan Harvest Salad due to potential Listeria monocytogenes contamination in sliced apples.
Pfizer is recalling specific lots of diphenoxylate hydrochloride and atropine sulfate tablets because weight variations caused some tablets to be sub-potent or super-potent.
Amendia, Inc. is recalling 40 Ceres Self-Drilling Variable Screws because some units marked as 12 mm actually measure 14 mm in length.
Harris Teeter is recalling Triple Chocolate Mini Biscotti because the product contains undeclared almonds. Consumers should check for Lot Number 17338.
Figi's, Inc. is recalling specific Dark Chocolate Gingersnaps because they contain undeclared milk, a major food allergen.
Casper's Ice Cream is recalling Caramel Cashew Ice Cream due to undeclared almonds, a major food allergen.
Philips is recalling 412 Mobile Detector Holders for Stationary X-ray Systems because the lock mechanism may fail, causing the detector to drop.
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