DrugMar 20, 2019
King Bio Dr. King's SafeCare Rx Children's Ear Relief Children High Potency Homeopathic recall — FDA D-0687-2019
Microbial contamination
Class IFDA: TerminatedKing Bio Inc.
Monthly breakdown
2019 recalls by month
Select a month to review the recall records reported during that period.
December 2019321 records · 4 categoriesNovember 2019597 records · 4 categoriesOctober 2019525 records · 4 categoriesSeptember 2019268 records · 4 categoriesAugust 2019505 records · 4 categoriesJuly 2019680 records · 4 categoriesJune 2019445 records · 4 categoriesMay 2019396 records · 4 categoriesApril 2019242 records · 4 categoriesMarch 2019250 records · 4 categoriesFebruary 2019381 records · 4 categoriesJanuary 2019142 records · 4 categories
2019 recalls — page 172
Records are ordered by the best available source date.
DrugMar 20, 2019
King Bio Dr. King's SafeCare Rx Colic Relief Children High Potency Homeopathic Formula for recall — FDA D-0681-2019
Microbial contamination
Class IFDA: TerminatedKing Bio Inc.
DrugMar 20, 2019
King Bio Dr. King's SafeCare Rx Influenza Multi-Strain Flu Medicine Immune High Potency recall — FDA D-0679-2019
Microbial contamination
Class IFDA: TerminatedKing Bio Inc.
DrugMar 20, 2019
King Bio Dr. King's SafeCare Rx Soothing Advanced Arnica Pure Homeopathic Cream High Potency recall — FDA D-0697-2019
Microbial contamination
Class IFDA: TerminatedKing Bio Inc.
DrugMar 20, 2019
King Bio Dr. King's SafeCare Rx Aversion to Change High Potency Homeopathic Formula for recall — FDA D-0984-2019
Microbial contamination
Class IFDA: TerminatedKing Bio Inc.
DrugMar 20, 2019
Macleods Pharma Usa Telmisartan and Hyrdochlorothiazide Tablets 40mg/12.5 mg, 30-count recall — FDA D-1003-2019
Failed Content Uniformity Specifications: The product is out of specification for blend uniformity.
Class IIFDA: TerminatedMacleods Pharma Usa Inc.
DrugMar 20, 2019
Docetaxel Injection USP, 80 mg/4 mL, (20 mg/mL), One-Vial Formulation recall — FDA D-1001-2019
Defective Container: complaint for seal and cap vial issues that could lead to a lack of sterility assurance.
Class IIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugMar 20, 2019
King Bio Dr. King's Natural Medicine Aquaflora Candida High Potency 9 Multi-Strain Candida recall — FDA D-0962-2019
Microbial contamination
Class IFDA: TerminatedKing Bio Inc.
DrugMar 20, 2019
Golean DETOX capsules, 14 Net: 56 g, 14 packets containing 2 capsules per packet, 28-count recall — FDA D-1009-2019
Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain undeclared sibutramine and phenolphthalein. Sibutramine is an appetite suppressant that was withdrawn from the…
Class IFDA: TerminatedGolean Detox US
DrugMar 20, 2019
King Bio Dr. King's SafeCare Rx Children's Fever Reliever Children High Potency Homeopathic recall — FDA D-0689-2019
Microbial contamination
Class IFDA: TerminatedKing Bio Inc.
DrugMar 20, 2019
Macleods Pharma Usa Telmisartan and Hyrdochlorothiazide Tablets 80 mg/25 mg, 30-count recall — FDA D-1005-2019
Failed Content Uniformity Specifications: The product is out of specification for blend uniformity.
Class IIFDA: TerminatedMacleods Pharma Usa Inc.
DrugMar 20, 2019
King Bio Dr. King's SafeCare Rx Breast Cyst & Discomforts High Potency Homeopathic Formula recall — FDA D-0985-2019
Microbial contamination
Class IFDA: TerminatedKing Bio Inc.
DrugMar 20, 2019
King Bio Dr. King's SafeCare Rx Attention & Learning Enhancement Children High Potency recall — FDA D-0677-2019
Microbial contamination
Class IFDA: TerminatedKing Bio Inc.
DrugMar 20, 2019
King Bio Dr. King's SafeCare Rx Lower GI Restoration Digestion High Potency Homeopathic recall — FDA D-0678-2019
Microbial contamination
Class IFDA: TerminatedKing Bio Inc.
DrugMar 20, 2019
King Bio Dr. King's SafeCare Rx Lonely Mind & Body High Potency Homeopathic Formula for recall — FDA D-0680-2019
Microbial contamination
Class IFDA: TerminatedKing Bio Inc.
VehicleMar 20, 2019
Volvo Car USA seats recall — NHTSA campaign 19V220000
Volvo Car USA LLC (Volvo) is recalling certain 2018-2019 XC60 and S90 vehicles. The driver and passenger front seat rail rear flange nuts may not have been installed during assembly.
seatsVolvo Car USA LLC
VehicleMar 20, 2019
Volkswagen Group of side/window recall — NHTSA campaign 19V218000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2019 Atlas and 2020 Passat vehicles. An incorrect driver and/or front passenger side impact air bag may have been…
side/windowVolkswagen Group of America, Inc.
VehicleMar 20, 2019
Honda Odyessy wheel speed sensor recall — NHTSA campaign 19V213000
Braun Corporation (Braun) is recalling certain 2018-2019 Honda Odyessy vehicles modified to be equipped with an in-floor wheelchair ramp conversion. The rear wheel speed sensor harnesses…
wheel speed sensorBraun Corporation
VehicleMar 14, 2019
Chrysler steering recall — NHTSA campaign 19V201000
Chrysler (FCA US LLC) is recalling certain 2019 Jeep Wrangler and 2019 Ram 1500 vehicles. These vehicles have improperly machined steering column stub shafts that may break, possibly…
steeringChrysler (FCA US LLC)
Medical DeviceMar 13, 2019
Microbiologics Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use recall — FDA Z-0982-2019
Cepheid Xpert Respiratory Control Panel (Catalog #8199) has an reduced expiration date from 24 months to 13 months.
Class IIFDA: TerminatedMicrobiologics Inc.
Medical DeviceMar 13, 2019
Siemens Medical Solutions USA Uroskop Omnia -fluoroscopic X-ray system Model # 10094910 The recall — FDA Z-0984-2019
The swivel arm holding the monitors may become dislodged from the carrying arm.
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceMar 13, 2019
Siemens Medical Solutions USA Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 recall — FDA Z-0985-2019
The swivel arm holding the monitors may become dislodged from the carrying arm.
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceMar 13, 2019
Draegar Medical Systems Omega Systems These devices are intended to be used in the recall — FDA Z-0975-2019
The firm is recalling their Delta family of patient monitors software due to cybersecurity vulnerabilities, which may cause the device to reboot, lose functionality, and/or lose…
Class IIFDA: OngoingDraegar Medical Systems, Inc.
Medical DeviceMar 13, 2019
GETINGE US SALES Maquet XS Flat Screen Monitor Holder, SAT XS32 12 SPE, Configuration Part recall — FDA Z-0990-2019
The affected flat screen monitor holders might not be compliant with grounding requirements. As a consequence, there is a risk of mild to severe/fatal electric shock under certain…
Class IIFDA: TerminatedGETINGE US SALES LLC
About the 2019 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.