💊 Drugs Class I - Dangerous
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
All Recalls
95,018 total recalls in our database
CITALOPRAM Tablets, USP, 20MG, 100 Tablets, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 0378-6232-01
CARDINAL HEALTHCARE
💊 Drugs Class I - Dangerous
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
FOLIC ACID TABLETS, USP, 1MG, 100 Tablets per bottle, Rx Only, Manufactured by: Leading Pharma, LLC, Fairfield, NJ 07004. NDC: 69315-127-10
CARDINAL HEALTHCARE
💊 Drugs Class I - Dangerous
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
💊 Drugs Class I - Dangerous
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
💊 Drugs Class I - Dangerous
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
💊 Drugs Class I - Dangerous
Presence of Particulate Matter.
Atrium Oasis Drain Single W / AC, Part No. 3600-100
Atrium Medical
🏥 Medical Devices Class I - Dangerous
A sterilization nonconformance prematurely aged the product by 48.3 days, resulting in the expiration date on the label not being accurate. This nonconforming product was inadvertently distributed to customers. Increased risk to patients and healthcare providers using the product after the shortened expiration date of November 17, 2025.
Landauer microSTARii reader, Medical Dosimetry System, Model Numbers: 18000-000/18001-000/18007-000
Landauer
🏥 Medical Devices Class I - Dangerous
MicroSTARii readers may be contributing to the nanodot dosimeter measurement inaccuracy in two possible ways. The first is related to the interaction of the reader s LED beam profile with the nanoDot dosimeter. The second is debris formation due to drawer actuation, resulting in a change of reader response that may not be detectable unless known dose QCs are being run regularly.
🏥 Medical Devices Class I - Dangerous
Due to potential breakage during use.
Alinity ci-series System Control Module, REF: 03R70-01
Abbott Laboratories
🏥 Medical Devices Class I - Dangerous
There are potential performance issues found in the Alinity ci-series System software versions 3.4.0 and lower, including: 1) SCC Reagent load error during daily maintenance; 2) Sample Laboratory Report error; 3) Customer requests mechanism to prevent user error when creating new lots of value assigned Calibrators; 4) Error in processing tests after CCCintController encountered an error with the assay information downloaded from SCC; 5) The assay editor does not correctly check sample dilution total volume limits; 6) User-Applied Labels not adhering to Reagent Bottles; 7) ICT Module did not expire after warranty was exceeded. These performance issues could lead to erroneous results for multiple analytes.
Medtronic SynchroMed II, Model 8637-20, Programmable pump
Medtronic Neuromodulation
🏥 Medical Devices Class I - Dangerous
Medtronic recently identified that if the SynchroMed II pump switches into telemetry mode due to electromagnetic interference (EMI) from an MRI scan, while the pump is sounding an alarm, the pump will not resume drug delivery after leaving the MRI magnetic field, which is inconsistent with the current labeling.
🏥 Medical Devices Class I - Dangerous
The component tracheostomy brush has a sharp edge at the tip that can potentially puncture tubing during use and/or cause user injury. Additionally, there have been incidents of the tracheostomy brush bristles detaching prior to use in the packaging and/or during use.
DeRoyal CARDIAC CATH SET-UP KIT PGYBK, REF 89-10572
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
Kit were manufactured and distributed with Edwards Life Sciences TruWave Disposable pressure transducers which were subsequently recalled by Edwards Life Sciences.
Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assembled with IndiGo Drive Assistance module and retrofitted with IndiGo Drive Assistance modules
ARJOHUNTLEIGH POLSKA Sp. z.o.o.
🏥 Medical Devices Class I - Dangerous
Unintended movement of bed wheels
Medtronic SynchroMed II, Model 8637-40, Programmable pump
Medtronic Neuromodulation
🏥 Medical Devices Class I - Dangerous
Medtronic recently identified that if the SynchroMed II pump switches into telemetry mode due to electromagnetic interference (EMI) from an MRI scan, while the pump is sounding an alarm, the pump will not resume drug delivery after leaving the MRI magnetic field, which is inconsistent with the current labeling.
Product Code 0848, MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode, Reusable Patient Return Electrode, Mega Soft Universal Dual Plus
Megadyne Medical Products
🏥 Medical Devices Class I - Dangerous
Affected product codes are now limited to use in patients age 12 years or older. Megadyne has received reports of patient burn injuries up to and including third-degree burns requiring intervention which may lead to prolonged hospital stay, scarring, and additional surgeries in both pediatric and adult patients.
Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assembled with IndiGo Drive Assistance module and retrofitted with IndiGo Drive Assistance modules
ARJOHUNTLEIGH POLSKA Sp. z.o.o.
🏥 Medical Devices Class I - Dangerous
Unintended movement of bed wheels
Product Code 0847, MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode, Reusable Patient Return Electrode, Mega Soft Universal Plus
Megadyne Medical Products
🏥 Medical Devices Class I - Dangerous
Affected product codes are now limited to use in patients age 12 years or older. Megadyne has received reports of patient burn injuries up to and including third-degree burns requiring intervention which may lead to prolonged hospital stay, scarring, and additional surgeries in both pediatric and adult patients.
Identification label on affected hookups could become illegible over time due to the label's ink coming off. This may potentially prevent users from being able to effectively identify the hookup and may ultimately result in postponement of patient procedures.
Product Code 0846, MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode, Reusable Patient Return Electrode, Mega Soft Universal Dual Cord
Megadyne Medical Products
🏥 Medical Devices Class I - Dangerous
Affected product codes are now limited to use in patients age 12 years or older. Megadyne has received reports of patient burn injuries up to and including third-degree burns requiring intervention which may lead to prolonged hospital stay, scarring, and additional surgeries in both pediatric and adult patients.