Archive
576 recalls were announced in November 2021.
Of the 576 recalls this month scored against our rubric, 0% are Critical, 44% are Severe.
Which agencies issued them
BioMerieux is recalling 1,382 API 50 CH diagnostic test kits because they may provide incorrect organism identification results, potentially leading to misdiagnosis.
Seneca Foods Corporation is recalling Aunt Nellie's and Happy Harvest sliced pickled beets due to inadequate acidity, which may allow botulism-causing bacteria to grow. The recall affects 15,074 cases distributed across 22 U.S. states.
Cook Inc. is recalling transseptal needles that may contain undetected rust, which could cause inflammatory reactions, systemic responses, and potentially permanent impairment.
OmniLife Science is recalling 7 units of the OMNI K2 Hip Stem due to missing grit blasting on the proximal surface, a defect that could lead to implant loosening and revision surgery. The recall affects units distributed to Colorado and Virginia.
CooperSurgical's LEEP PRECISION System may fail to coagulate tissue when using the hand switch, potentially requiring medical intervention to control intraoperative bleeding during procedures.
Bayer Healthcare is recalling Lotrimin AF Miconazole nitrate 2% Liquid Spray nationwide due to potential benzene contamination. The product was manufactured at a facility where other lots were found to contain benzene.
Bayer Healthcare Pharmaceuticals is recalling Lotrimin AF (Tolnaftate 1%) Daily Prevention deodorant powder spray due to potential benzene contamination. The product was manufactured at a facility where other lots were found contaminated with benzene.
Beaver Visitec International recalls CustomEyes Cataract Surgical Kits containing Xstar Crescent Knives with incorrect blade orientation. Kits labeled as 55-degree bevel-down blades actually contain bevel-up blades.
Cordis Corporation is recalling 3 units of SMART FLEX 6x120 BIL biliary stents due to a potential for distal tip dislodgement or separation. No illnesses or injuries have been reported.
ROi CPS LLC is recalling the REGARD Ear Tray because it contains a Povidone-Iodine swabstick component that does not meet specifications. The product was distributed in Florida, Louisiana, and Missouri.
ROi CPS LLC recalled REGARD Stereotactic Trays due to out-of-specification Povidone-Iodine swabstick components. The recall affects 175 units distributed in Florida, Louisiana, and Missouri.
Cordis is recalling the SMART FLEX 6x150 BIL biliary stent system due to potential separation of the distal tip. Approximately 26 units were distributed in the U.S. and Canada. Affected patients should contact their healthcare provider.
Alamo Group is recalling 2019-2021 Old Dominion Brush Co. trailers because incorrect wiring may prevent the emergency brake from engaging if the trailer detaches.
Approximately 5950 Beaver Xstar Crescent Knife surgical blades may be packaged with the wrong bevel angle, potentially affecting proper surgical technique during cataract procedures.
Permobil TiLite wheelchairs (Models Aero Z and ZRA) used as vehicle passenger seats may not be properly oriented during motor vehicle accidents due to transit tie-down configuration issues. Consumers should discontinue use as passenger seats until replacement tie-downs are installed.
Cordis Corporation is recalling 9 SMART FLEX 9x60 biliary stent units due to a potential for distal tip dislodgement or separation. The stents were distributed to patients in several U.S. states and Canada.
Cordis Corporation is recalling the SMART FLEX Biliary Stent System (Lot 266586) due to potential distal tip dislodgement or separation. Affected units were distributed to select US states and Canada.
CooperSurgical is recalling 75 units of the LEEP PRECISION Generator 220V because the coagulation hand switch may fail, potentially causing uncontrolled bleeding during surgery.
ROi CPS LLC is recalling REGARD Newborn Trays (lot 86453F) distributed in FL, LA, and MO because some units contain a povidone-iodine swabstick component manufactured out of specifications.
Carolina Ingredients is recalling Mustard & Onion Seasoning due to possible lead contamination. The product was distributed to one customer in Georgia.
Teva Pharmaceuticals USA is recalling Cartia XT (Diltiazem Hydrochloride Extended-Release Capsules, USP) 120 mg due to an incorrect expiration date printed on the label. The affected lot was distributed nationwide.
Newly Weds Foods Inc is recalling 50 lb. bags of corn dog batter due to the potential for metal contamination in the product.
Amneal Pharmaceuticals is recalling Flocinolone Acetonide 0.01% Topical Oil due to an out-of-specification assay result indicating the drug is subpotent and may not deliver the intended therapeutic dose.
Teva Pharmaceuticals USA is recalling 64,978 Clonidine Transdermal System patches (0.1 mg/day) due to failed specifications for impurities and degradation. The recall affects nationwide and Puerto Rico distribution.
Fujifilm Irvine Scientific is recalling Vit Kit-Freeze, a medical device used in assisted reproductive procedures, due to kit components being labeled with incorrect expiration dates.
ROi CPS LLC is recalling 22 REGARD Vitrectomy Trays because the povidone-iodine swab component was manufactured out of specifications. Distribution was limited to Florida, Louisiana, and Missouri.
Church Brothers, LLC is recalling True Leaf VA Romaine Chopped lettuce due to plastic pieces found in the product. The affected lot was distributed in Maryland.
Amneal Pharmaceuticals is recalling Flocinolone Acetonide 0.01% Topical Oil because testing found out-of-specification assay results, meaning the drug may contain less active ingredient than labeled.
Newly Weds Foods Inc is recalling Scampi Seasoning in 50 lb. bags due to the potential for metal contamination in the product.
Bayer Healthcare Pharmaceuticals is recalling Lotrimin AF Daily Prevention deodorant powder spray due to cGMP deviations at the manufacturing facility where other lots were found contaminated with benzene.
CooperSurgical is voluntarily recalling 154 Quantum 2000 Electrosurgical Generators under FDA Class II classification. The specific reason for recall is not documented in available source information.
Fujifilm Irvine Scientific is recalling Vit Kit-Freeze due to incorrect expiration date labeling on a component. The incorrect label could lead to use of degraded solutions in assisted reproductive procedures.
Ortho-Clinical Diagnostics recalled 191 units of VITROS Anti-HBc IgM Controls (Lot 1690) because the Controls Values booklet contained incorrect product information. Although patient test result accuracy is not affected, there is potential for delayed quality control troubleshooting.
Toyota is recalling 2007-2021 Tundra and 2008-2022 Sequoia vehicles due to defective power steering gear assemblies that can leak oil, causing sudden loss of power steering assist and increased crash risk.
Daimler Trucks North America is recalling 2017-2023 Freightliner Custom Chassis trucks due to damaged tire valve stem extensions that may lose pressure, increasing crash risk. Dealers will remove the valve stem extensions and stabilizers at no charge.
Ford is recalling 2021-2022 Escape and Bronco Sport vehicles with rear brake linings that may have been manufactured incorrectly. This can affect braking performance, extending stopping distance and increasing crash risk.
Chrysler is recalling specific Mopar Trailer Reverse Steering Control Modules that may prevent the rearview image from displaying, increasing crash risk.
Chrysler is recalling 2022 Jeep Wagoneer and Grand Wagoneer vehicles because the rear center-seat recliner strap may prevent the seat back from locking into the upright position. This defect increases crash injury risk and violates Federal Motor Vehicle Safety Standard 207.
Chrysler is recalling 2021 RAM 1500 pickup trucks because the rearview camera display may stop working, violating federal rear-visibility standards. Dealers will provide a software update.
Impex Fitness is recalling about 77,200 Olympic Dumbbell Handles because the locking collars can slip, causing weights to drop and potentially cause impact injuries. No injuries have been reported to date.
2022 Nissan Frontier Crew Cab Long Bed trucks lack an installed tow hitch, compromising fuel tank structural integrity. In a rear crash, the leaf spring could contact the fuel tank, risking fire or injury.
Vermeer is recalling 2018-2022 vacuum excavators because operator manuals list incorrect lug nut tightness values, which could lead to wheel detachment.
Daimler Trucks North America is recalling one 2020 Thomas Built Buses Saf-T-Liner HDX transit bus because it lacks required electronic stability control hardware and software.
Daimler Trucks North America is recalling one 2021 Thomas Built Buses Saf-T-Liner HDX transit bus because the gross axle weight rating label may be incorrect.
Tesla is recalling 2020-2022 Model Y vehicles because front and rear suspension knuckles may fracture, potentially causing suspension links to separate and increasing crash risk.
KME is recalling 2021-2022 Predator emergency vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake unexpectedly and increasing crash risk.
BMW is recalling specific 2013-2018 diesel models because an EGR cooler leak can cause a melting intake manifold, increasing the risk of a fire.
Mercedes-Benz is recalling 2021 GLE 450 and AMG GLE53 vehicles because improperly tightened bolts on the electric heater may cause wiring to overheat, increasing the risk of a fire.
PACCAR is recalling approximately 908 Peterbilt and Kenworth commercial trucks from 2019-2022 for a brake defect that may cause unintended vehicle movement during winching operations. Software updates will be provided free of charge.
Ferrara is recalling 2021-2022 Inferno and Cinder emergency vehicles because a rear axle drive pinion may fracture, increasing crash risk.
Porsche is recalling 2020 Taycan vehicles because loose rear axle screw connections may fail, causing loss of stability and increasing crash risk.
Key Safety Systems (Joyson) is recalling specific curtain air bag inflators that may contain incorrect gas amounts, potentially causing improper deployment and increasing injury risk in crashes.
Forest River is recalling 2021-2022 Impression Fifth Wheel RVs due to incorrectly positioned center identification lights that fail to meet federal lighting standards. The defect reduces visibility and increases crash risk.
The remote controller for the passenger-side power sliding door may malfunction, preventing secure latching. A failure could allow the door to open while driving, increasing injury risk.
E-One is recalling 2022 Cyclone and Typhoon vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake and increasing crash risk.
ATC is recalling 2021 Raven and Quest trailers because incorrect fasteners on the ramp door cables may cause bushing failure, increasing the risk of injury.
Spartan Fire is recalling 2020-2022 MetroStar, FC-94, and Gladiator emergency vehicles because a rear axle drive pinion may fracture, increasing crash risk.
Goodman Manufacturing is recalling evaporator coil drain pans used in residential gas furnaces because the plastic drain pan can overheat, melt, and deform, posing a fire hazard. The company has received 23 reports of fire incidents involving the drain pans, resulting in significant fire and smoke damage to residences.
Honda is recalling 2021 NC750XD motorcycles because incorrect fuel injection software may cause stalling, increasing crash risk.
Honda is recalling certain 2021 Accord and other model vehicles because the automatic locking retractor on the second-row center seat belt may deactivate improperly, potentially leaving child restraints unsecured in a crash.
Jayco is recalling 2021 Jay Flight Octane travel trailers because the water heater was installed in the wrong location, which could allow exhaust fumes to enter the trailer.
American Honda is recalling about 1,400 Honda Pioneer 700, Pioneer 1000, and Talon 1000 recreational off-highway vehicles equipped with electric power steering. The vehicles can lose steering function, posing crash and injury hazards.
Amazon is recalling about 15,300 AmazonBasics Memory Foam Mattresses sold between April 2020 and March 2021 because they fail to meet federal flammability standards, posing a fire hazard. No injuries have been reported.
Toyota is recalling 2018-2019 Camry vehicles because a vacuum pump component may break, causing a sudden loss of braking assist and increasing crash risk.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling one lot of QUAD-MIX PAPAV 30/PHENTOL 2/PGE-1 20/ATROPINE 0.2 INJ injectable due to lack of assurance of sterility.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling testosterone cypionate 200mg/anastrozole 1mg/ml injectable vials distributed across the United States, Puerto Rico, and Washington, D.C. due to lack of assurance of sterility.
Talon Compounding Pharmacy is recalling a testosterone cypionate and anastrozole injectable product because the manufacturer cannot assure sterility. The product was distributed across the United States, Washington, D.C., and Puerto Rico.
Talon Compounding Pharmacy is recalling Estradiol Valerate 40mg/mL injectable across the United States due to lack of assurance of sterility. The affected product was distributed in 11 vials with multiple lot numbers.
Sutphen is recalling 2020 Fire trucks because pressure in the power steering pump may break the shaft seal, causing a loss of steering assist and increasing crash risk.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Test Cypionate 200mg/Anastrozole 0.5mg/Dutasteride 1mg/ml injectable (4 vials) due to lack of assurance of sterility.
Talon Compounding Pharmacy is recalling MIC B Complex with Hydroxocobalamin 5MG/ML injectable vials due to lack of assurance of sterility. The recall affects vials distributed across the United States.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling an injectable compounded drug product containing testosterone cypionate, anastrozole, and dutasteride due to lack of assurance of sterility. The product was distributed in the United States including Washington, D.C. and Puerto Rico.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling an injectable steroid combination product due to lack of assurance of sterility. The recall affects 13 vials distributed across the United States, including Washington, D.C. and Puerto Rico.
Talon Compounding Pharmacy is recalling injectable medications containing testosterone cypionate, anastrozole, and dutasteride due to lack of assurance of sterility. The recall affects 23 vials distributed across the United States.
Talon Compounding Pharmacy is recalling Methylcobalamin 5MG/ML injectable (Lot 07162021:70) distributed nationwide because the manufacturer cannot assure sterility of the product.
Talon Compounding Pharmacy is recalling Tri-Mix Papaverine injectable medication because the manufacturer cannot guarantee sterility. The affected injectable product was distributed across the United States.
Vita Pharmacy (Talon Compounding) is recalling TRI-MIX injectable medication (Lot 07142021:43) distributed across the United States because the manufacturer cannot assure the product meets sterility standards.
Talon Compounding Pharmacy is recalling Ultra-Test (CYP 80%/PROP 20%) 200mg/ml injectable across the United States, Puerto Rico, and Washington, D.C. due to lack of assurance of sterility.
Vita Pharmacy (Talon Compounding Pharmacy) is recalling two lots of testosterone cypionate 200mg/anastrozole 0.7mg/ml injectable solution due to lack of assurance of sterility. The product was distributed nationwide.
Talon Compounding Pharmacy is recalling TRI-MIX PAPAVERINE 18/PHENTOL 0.6/PGE-1 6/ML injectable medication due to lack of assurance of sterility. The product was distributed across the United States, including Washington, D.C. and Puerto Rico.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Testosterone Cypionate 200mg/ml injectable due to lack of assurance of sterility. The product was distributed across the United States, including Washington, D.C. and Puerto Rico.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Tri-Mix Papaverine 15/Phentolamine 1/PGE-1 10 injectable vials due to lack of assurance of sterility. The affected lot (09082021:40, BUD 02/08/2022) was distributed throughout the United States including Washington, D.C. and Puerto Rico.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling 22 vials of TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 20 injectable due to lack of assurance of sterility. The product was distributed across the United States including Washington, D.C. and Puerto Rico.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling TRI-MIX PAPAVERINE 30/PHENTOLAMINE 4/PGE-1 7.5/ML injectable due to lack of assurance of sterility. The product was distributed across the United States, including Washington, D.C. and Puerto Rico.
Talon Compounding Pharmacy is recalling an injectable steroid combination product (Test Cypionate 200mg/Anastrozole 2mg/Dutasteride 2mg/mL) due to lack of assurance of sterility. The affected lot was distributed nationwide.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling QUAD-MIX PAPAV 20/PHENTOL 2/PGE-1 25/ATROPINE 0.2 INJ due to lack of assurance of sterility. The recall affects one lot distributed across the United States, Washington D.C., and Puerto Rico.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling a compounded injectable product containing testosterone cypionate, anastrozole, and dutasteride due to lack of assurance of sterility. The recall affects lot T1009092021:19 distributed across the United States.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Sermorelin Acetate 9mg/Ipamorelin 9mg lyophilized vials (Lot 08102021:22) distributed in the United States due to lack of assurance of sterility.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Tri-Mix Papaverine/Phentolamine/PGE-1 injectable vials distributed across the United States and Puerto Rico due to lack of assurance of sterility.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Testosterone Cypionate 30mg/mL injectable due to lack of assurance of sterility. The affected lot was distributed across the United States, Washington D.C., and Puerto Rico.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling testosterone cypionate 20 mg/mL injectable due to lack of assurance of sterility. The product was distributed across the United States, Washington D.C., and Puerto Rico.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling a compounded injectable drug containing testosterone cypionate, anastrozole, and dutasteride due to lack of assurance of sterility.
Talon Compounding Pharmacy is recalling TRI-MIX PAPAVERINE 30/PHENTOLAMINE 0.5/PGE-1 10 injectable vials because the manufacturer cannot assure sterility of the product.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling an injectable drug product due to lack of assurance of sterility. The product was distributed across the United States, including Washington, D.C. and Puerto Rico.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling a compounded injectable medication (Quad-Mix Papav 30/Phentol 1/PGE-1 10/Atropine 0.15) due to lack of assurance of sterility. The affected lot was distributed across the United States, Washington D.C., and Puerto Rico.
Talon Compounding Pharmacy is recalling Estradiol Valerate 50mg/ml Injectable (Lot 09162021:22) distributed across the United States because the manufacturer cannot assure the product's sterility.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Tri-Mix Papaverine 30/Phentolamine 3/PGE-1 100 injectable due to lack of assurance of sterility. The affected lot was distributed across the United States, including Washington, D.C. and Puerto Rico.
Volkswagen is recalling certain 2021 Atlas and 2020-2021 Cross Sport vehicles whose air conditioning drain tube can become blocked, allowing water to damage the air bag control module and potentially trigger inadvertent air bag deployment.
Talon Compounding Pharmacy is recalling TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 25 injectable medication due to lack of assurance of sterility. The product was distributed across the United States, Washington, D.C., and Puerto Rico.
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Testosterone Cypionate 200mg/Anastrozole 1.5mg/mL injectable due to lack of assurance of sterility. The product was distributed in the United States including Washington, D.C. and Puerto Rico.
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