DrugApr 15, 2020
Herbal Doctor Remedies Acupuncture recall — FDA D-1105-2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Class IIFDA: TerminatedHerbal Doctor Remedies
April 2020 recalls — page 11
These records include useful source details for the selected month.
DrugApr 15, 2020
Avet Pharmaceuticals Losartan Potassium Tablets USP 100 mg, supplied in a) 30 count recall — FDA D-1104-2020
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level
Class IIFDA: TerminatedAvet Pharmaceuticals, Inc.
DrugApr 15, 2020
PharMEDium Services ePHEDrine Sulfate 5 mg per mL 25 mg per 5 mL, in 0.9% Sodium Chloride, 5 recall — FDA D-1090-2020
Firm is recalling 46 lots of various products because of a lack of sterility assurance.
Class IIFDA: TerminatedPharMEDium Services, LLC
DrugApr 15, 2020
Herbal Doctor Remedies Fungo Off, 500mg Capsules, 90-count bottles recall — FDA D-1128-2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugApr 15, 2020
Herbal Doctor Remedies Skin Moist, 500mg Capsules, 90-count bottles recall — FDA D-1161-2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugApr 15, 2020
Herbal Doctor Remedies Fungo Balm recall — FDA D-1125-2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugApr 15, 2020
PharMEDium Services succinylcholine Chloride, 20 mg per 5 mL, 100 mg per 5 mL, 5 mL BD recall — FDA D-1086-2020
Firm is recalling 46 lots of various products because of a lack of sterility assurance.
Class IIFDA: TerminatedPharMEDium Services, LLC
DrugApr 15, 2020
Herbal Doctor Remedies Thyro-Lo, 500mg Capsules, 90-count bottles recall — FDA D-1166-2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugApr 15, 2020
Herbal Doctor Remedies Age Back, 500 mg Capsules, 90-count bottles recall — FDA D-1108-2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugApr 15, 2020
Herbal Doctor Remedies Lump Shrinker, 500mg Capsules, 90-count bottles recall — FDA D-1141-2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugApr 15, 2020
Herbal Doctor Remedies Pain Away, 500mg Capsules, 90-count bottles recall — FDA D-1147-2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugApr 15, 2020
Herbal Doctor Remedies Tution 130 recall — FDA D-1167-2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugApr 15, 2020
Herbal Doctor Remedies Stomach Cleanser, 500mg Capsules, 90-count bottles recall — FDA D-1163-2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugApr 15, 2020
Herbal Doctor Remedies Phlegm Off, 500mg Capsules, 90-count bottles recall — FDA D-1150-2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugApr 15, 2020
Herbal Doctor Remedies Acne Cystic, 500 mg Capsules, 90-count bottles recall — FDA D-1106-2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugApr 15, 2020
Herbal Doctor Remedies Dermatoxin, 500mg Capsules, 90-count bottles recall — FDA D-1117-2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugApr 15, 2020
Herbal Doctor Remedies Herpes-G, 500mg Capsules, 90-count bottles recall — FDA D-1132-2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugApr 15, 2020
Herbal Doctor Remedies Detoxin-S, 500mg Capsules, 90-count bottles recall — FDA D-1120-2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugApr 15, 2020
Herbal Doctor Remedies Edema Off recall — FDA D-1122-2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Class IIFDA: TerminatedHerbal Doctor Remedies
VehicleApr 9, 2020
Hyundai Motor electrical system software recall — NHTSA campaign 20V213000
Hyundai Motor America (Hyundai) is recalling certain 2020 Nexo and Sonata vehicles. The Remote Smart Parking Assist (RSPA) software may fail to prevent vehicle movement upon detection of an…
electrical system softwareHyundai Motor America
VehicleApr 9, 2020
Chrysler structure recall — NHTSA campaign 20V207000
Chrysler (FCA US LLC) is recalling certain 2019-2020 Ram 2500 and Ram 3500 Pick-up trucks equipped with an accessory bed step. In certain side loading conditions, the bed step may…
structureChrysler (FCA US LLC)
VehicleApr 9, 2020
Chrysler linkages recall — NHTSA campaign 20V208000
Chrysler (FCA US LLC) is recalling certain 2019-2020 Ram 1500, 1500 Classic and Jeep Compass vehicles. The windshield wiper arm or arms may loosen, possibly causing the wipers to not…
linkagesChrysler (FCA US LLC)
Medical DeviceApr 8, 2020
DeRoyal SECURITY CUFFS, Single Strap, QR Buckle Cuff and Bed, UNIVERSAL, REF M8138 - Product recall — FDA Z-1604-2020
One lot of product was inadvertently manufactured with a buckle which does not meet the mechanical hold force required for this device.
Class IIFDA: TerminatedDeRoyal Industries Inc.
Medical DeviceApr 8, 2020
Trilliant Surgical Instructions for Use and Surgical Cleaning and Sterilization Protocol for recall — FDA Z-1613-2020
Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018.
Class IIFDA: TerminatedTrilliant Surgical, LLC
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.