Archive
815 recalls were announced in February 2020.
Of the 815 recalls this month scored against our rubric, 11% are Critical, 23% are Severe.
Which agencies issued them
Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because steering spindle screws may loosen, increasing crash risk.
Keystone RV Company is recalling 2020 Crossroads Zinger, Hideout, and Springdale trailers because spare tire carrier U-bolts may fail, allowing the carrier and tire to detach.
Rosenbauer is recalling one 2018 Commander emergency vehicle because the foam pump system can overheat and fail, making firefighting foam unavailable.
Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because the steering column casing cover may be missing, potentially allowing debris to interfere with steering.
McNeilus is recalling specific ZF CML12 Ring Gear Carriers because cavities in the toothing may cause premature drum transmission failure, increasing crash risk.
Mercedes-Benz is recalling one 2019 Smart Fortwo Electric Drive because a battery weld may detach, causing sudden failure, stalling, or fire.
HME is recalling 2016-2020 AF1, 1871, and SFO emergency vehicles because a missing O-ring seal may allow moisture into the fuse box, potentially causing overheating or malfunction.
Terex is recalling 2014-2019 TM bucket/boom trucks because an upside-down limit switch may fail to stop platform tilting, increasing injury risk.
Kia is recalling 2011-2012 Sedona vehicles because the fuel rail may crack and leak, increasing the risk of fire.
Kia is recalling 2013-2014 Optima vehicles because a low-pressure fuel hose may crack and leak, increasing the risk of a fire.
The 2021 Ford E-350 may have inadequate rear axle differential fluid, risking driveshaft separation and loss of drive. Ford will inspect and adjust or replace the rear axle assembly at no cost.
Ford is recalling 2018-2020 F-150 trucks because daytime running lamps may fail to dim, reducing visibility for other drivers and increasing crash risk.
Ford is recalling 2015-2016 F-150 trucks with 3.5L GTDI engines because a misplaced block heater could damage a cable, increasing the risk of a fire.
CHTC Bus Group is recalling 2016-2018 HT-35 and HT-45 buses because their wheelchair platform lifts failed to complete the required compliance certification process.
Meritor is recalling specific steer axles due to insufficient lubrication that may damage wheel end bearings. This defect could cause the wheel to separate, leading to a loss of vehicle control.
Kolcraft is recalling inclined sleeper accessories for two bassinet models to prevent infant suffocation. Consumers should stop using the accessory immediately.
Browning is recalling approximately 1,265 leather pistol holsters because the design can inadvertently change the firearm's safety switch position, posing an injury risk.
Interamerican Auto Parts is recalling specific KelvinHID HID bulbs because their light output may be incorrect and blind oncoming traffic, failing federal safety standards.
SMC Trailers is recalling 2019-2020 Laramie trailers because the Federal Placard lists the incorrect tire PSI, which may lead to overinflation and tire failure.
ADM Milling is recalling 5,000 bags of Best Baker's flour because of a potential E. coli O26 contamination. The recall covers 13 states.
ADM Milling is recalling 762,720 bags of King Arthur All-purpose Flour due to a potential E. coli O26 contamination risk.
ADM Milling is recalling 1,900 bags of H & R All Purpose Flour because it may be contaminated with E. coli O26.
ADM Milling is recalling 88,250 bags of Balancer flour because of a potential E. coli O26 contamination. The product was distributed across 13 states.
ADM Milling is recalling 62,400 bags of Robin Hood All-purpose Flour due to E. coli O26 contamination. The recall covers 13 states.
ADM Milling is voluntarily recalling bulk flour distributed to 13 states due to potential E. coli O26 contamination. The recall was initiated in September 2019 and terminated in September 2020.
RemedyRepack Inc. is recalling 75 vials of Ketorolac Tromethamine 30 mg/1mL injections distributed in Oklahoma and Louisiana due to the presence of small black particles.
ADM Milling is recalling 1,000 bags of Springup Flour because of a potential E. coli O26 contamination. The product was distributed to 13 states.
ADM Milling is recalling 300 bags of Sir Lancelot HG Flour because it may be contaminated with E. coli O26. The product was distributed to 13 states.
Teleflex Medical is recalling 127,293 Hudson RCI Comfort Flo Humidification Systems nationwide due to a potential risk of water flooding the column and entering the circuit during high-flow oxygen therapy.
ADM Milling is voluntarily recalling 950 bags of Commander Flour because it may be contaminated with E. coli O26.
ADM Milling is voluntarily recalling 2,550 bags of H&R Flour because of potential E. coli O26 contamination. The recall covers products distributed to 12 states.
ADM Milling is recalling 4,250 bags of Commander Flour because it may be contaminated with E. coli O26. The product was distributed to 13 states.
Teleflex Medical is recalling 95,696 Hudson RCI Comfort Flo Humidification Systems due to a potential risk of water flooding the column and entering the patient circuit during high-flow oxygen therapy.
ADM Milling is recalling 204,960 bags of Bakers Corner All Purpose Flour because it may be contaminated with E. coli O26.
Pacific Medical Group is recalling 466 Toco M2734A fetal monitors serviced with unverified non-OEM components that may fail to detect fetal distress or cause burns.
ADM Milling is recalling 24,990 bags of PB 25 LBS All Purpose Flour because it may be contaminated with E. coli O26. The recall covers 13 states.
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.
Pacific Medical Group Inc. is recalling Toco MP Transducers serviced with unverified non-OEM components. The defect may cause inaccurate fetal monitoring and patient burns.
Contract Pharmacal is recalling Leader Extra Strength Acetaminophen tablets due to a complaint about a foreign prenatal tablet found in the bottle.
Arrow International is recalling 343,105 epidural catheterization kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Market America is recalling 1,496 bottles of bliss anti-stress formula dietary supplement due to potentially undeclared Yohimbe and reported adverse reactions.
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.
Arrow International is recalling specific lots of Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.
Pfizer is recalling 38,676 trays of Fentanyl Citrate Injection vials because loose metal overseal crimps may compromise sterility.
Arrow International is recalling 343,105 epidural catheterization kits because the included syringes may fail, potentially causing dural puncture.
Terumo is recalling 33 Advanced Perfusion System 1 Roller Pumps because the pump shafts may fail, potentially causing the pump to stop during surgery.
Arrow International Inc is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Arrow International Inc. is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Arrow International is recalling FlexTip Plus Combined Spinal Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.
Pacific Medical Group is recalling 1,994 ultrasound transducers serviced with unverified non-OEM components, which may cause inaccurate fetal and maternal monitoring.
B and A Trading Corporation is recalling 40 packages of Kushim Tablets marketed without FDA approval. Analysis found the product contains unapproved active ingredients.
Teleflex Medical Inc. is recalling Rusch Greenlite Single-Use Metal Laryngoscope Blades because they may break at a welded joint during setup or use.
Arrow International Inc is recalling 10 cc Luer-Slip Loss of Resistance Syringes due to potential failures that could result in dural puncture.
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.
AuroMedics Pharma LLC is recalling 30,432 bottles of Amoxicillin and Clavulanate Potassium tablets because a customer complaint identified a nylon cable tie as a foreign substance.
Arrow International is recalling TheraCath Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits due to potential syringe failures that could cause dural puncture.
Arrow International is recalling 343,105 epidural catheterization kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Microvention is recalling 392 units of AZUR Peripheral Coil Systems because the implant coil may be missing from the devices.
Arrow International is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Arrow International is recalling FlexTip Plus Combined Spinal Epidural Catheterization Kits due to potential syringe failures that could cause dural puncture.
Pacific Medical Group is recalling Loop-Style Tocotransducers serviced with unverified non-OEM components, which may cause inaccurate fetal monitoring or patient burns.
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.
Efficient Laboratories, Inc. is recalling 4,080 bottles of Rompe Pecho MAX Multi Symptoms due to microbial contamination. Consumers should stop using the product and return it to the point of purchase.
Arrow International is recalling 343,105 epidural catheterization kits because the included syringes may fail, potentially causing dural puncture.
Arrow International Inc is recalling FlexTip Plus Combined Spinal Epidural Catheterization Sets because the included loss of resistance syringes may fail, potentially causing dural puncture.
Arrow International is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Pacific Medical Group is recalling 6,481 Button-Style Ultrasound Transducers serviced with unverified non-OEM components. The defect may cause inaccurate fetal and maternal monitoring or patient burns.
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.
Arrow International is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Arrow International is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Arrow International is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.
Arrow International is recalling FlexTip Plus Combined Spinal Epidural Catheterization Kits due to potential syringe failures that could cause dural puncture.
Arrow International Inc is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
ADM Milling is recalling 1,600 bags of Bova Flour HG in 50 lb bags due to potential E. coli O26 contamination. The product was distributed to 13 states.
ADM Milling is recalling 200 bags of Polar Bear Flour UNTR because it may be contaminated with E. coli O26. The product was distributed to 13 states.
Taro Pharmaceuticals is recalling Lamotrigine Tablets 100 mg because they were cross-contaminated with enalapril maleate. The affected lot was distributed nationwide in the U.S. and Puerto Rico.
Arrow International is recalling FlexTip Plus Epidural Catheterization Sets for pediatric lumbar placement because the included loss of resistance syringes may fail, potentially causing dural puncture.
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.
Arrow International is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Terumo is recalling 11 Advanced Perfusion Assembly Pump Guts units because pump shafts may fail, potentially causing the pump to stop during surgery.
Arrow International is recalling FlexTip Plus Epidural Catheterization Sets because the included syringes may fail, potentially causing dural puncture.
Teleflex Medical is recalling Rusch Greenlite Single-Use Metal Laryngoscope Blades because they may break at a welded joint during setup or use.
ADM Milling is recalling 1,700 bags of H & R All Purpose Flour because of a potential E. coli O26 contamination. The product was distributed across 13 states.
Efficient Laboratories is recalling 5,249 bottles of Rompe Pecho CF Cold & Flu with Honey due to microbial contamination. The product was distributed nationwide in the USA.
Pacific Medical Group is recalling 2,170 Toco+ transducers serviced with unverified non-OEM components. The defect may cause inaccurate fetal/maternal monitoring and patient burns.
ADM Milling is recalling 1,600 bags of Sir Galahad flour because it may be contaminated with E. coli O26. The recall covers 13 states.
Arrow International is recalling FlexTip Plus Epidural Catheterization Sets because the included syringes may fail, potentially causing dural puncture.
Efficient Laboratories, Inc. is recalling 5,387 bottles of Rompe Pecho EX Expectorant due to microbial contamination. Consumers should stop using the product and return it to the place of purchase.
Arrow International Inc is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Adm Milling is recalling 11,074 bags of King Arthur All Purpose Flour due to potential E. coli O26 contamination. The recall covers 13 states.
Akorn Inc is recalling 16,078 bottles of Hydrocortisone and Acetic Acid Otic Solution due to low assay results for the hydrocortisone component.
ADM Milling is recalling 7,400 bags of Potentate flour because it may be contaminated with E. coli O26. The recall covers distribution in 13 states.
Arrow International is recalling FlexTip Plus Epidural Catheterization Sets because the included syringes may fail, potentially causing dural puncture.
Arrow International Inc is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Arrow International Inc is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Medtronic is recalling specific 640G insulin pumps due to a loose reservoir that may cause incorrect insulin delivery.
Pacific Medical Group is recalling 5,897 ultrasound transducers serviced with unverified non-OEM components, which may cause inaccurate monitoring or patient burns.
Pacific Medical Group is recalling Loop-Style Ultrasound Transducers serviced with unverified non-OEM components. The parts may cause inaccurate fetal monitoring and patient burns.
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