Medicine, medical device and cosmetics recalls in United States
Recalls of medicines, medical devices, supplements, cosmetics and personal care products published in United States, newest first.
1,518 recalls, newest first · Checked 16 minutes ago
United StatesGlenmark Pharmaceuticals Inc., USA recalls Bisoprolol Fumarate and Hydrochlorothiazide Tablets
Cross Contamination with Other Products: Testing of reserve samples showed presence of traces of ezetimibeRemel, Inc recalls 1. CAMHB W/LHB
Products may contain contamination, which may result in a darker or brown media color.Philips Medical Systems Nederland B.V. recalls Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234
The motorized longitudinal movement of the FlexArm stand may be inconsistent (not smooth) and eventually may become unavailable.BioFire Diagnostics, LLC recalls BioFire Respiratory Panel 2.1
Due to unintended movement of pouch chemistry, nucleic acid test may result in elevated risk of false negative results and risk of control failures.Medtronic Sofamor Danek USA Inc recalls Catalyft PL & PL40 Expandable Interbody System labeled as follows with corresponding…
Expandable interbody system cage may loose height or collapse (loss of lordosis), which could result in migration, subsidence and/or neurological injury.Intelerad Medical Systems Incorporated recalls IntelePACS
Software application that receives digital images and data to be communicated, processed, manipulated, enhanced, stored, displayed has a bug that could cause data loss…Magellan Diagnostics, Inc. recalls The LeadCare¿ II Blood Lead Test System relies on electrochemistry and a unique Sensor…
Calibration Buttons being used in the kitting process were incorrectly labeled as Lot 2323M for lot 2333M.Inpeco S.A. recalls FlexLab and 1 more products
The Aliquoter Module (mALX) may generate secondary sample tubes without labels or with mismatched labels which may result in delayed results or erroneous results.Olympus Corporation of the Americas recalls Brand Name: EVIS EXERA III Duodenovideoscope Product Name: Olympus TJF-Q190V…
Continued reports of positive cultures and infections have identified updates to the reprocessing materials to minimize potential deviations in TJF duodenoscope…Djo, LLC recalls Cold Form Wrap: Back
The IFU (Information for Use) on the wrap instructs the user to heat the hot and cold compression wrap in the microwave for 3 minutes, which may cause the wrap to leak…Pivotal Health Solutions, Inc. recalls Quantum Intersegmental Table and 1 more products
The heat function may become damaged over time due to patients pressing on the areas with heat function components.Glycar SA Pty., Ltd. recalls SJM Pericardial Patch and 1 more products
The impacted lot may not meet the required tensile strength specification.Dermasensor Inc recalls DermaSensor. Model/Catalog Number: 10101. Software Version: 3.0.2. Software-aided…
Potential for device to not meet specifications resulting in incorrect results or delay of referral for patients.Alcon Research LLC recalls CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K
XXXOlympus Corporation of the Americas recalls Brand Name: Single Use Ligating Device Product Name: Olympus HX-400U-30 Model/Catalog…
Potential that the ligation loop was unable to release or detach as expected during use, causing the loop to become unintentionally fixed around patient anatomy.Medtronic MiniMed, Inc. recalls CareLink Clinic
Software error causing incorrect data to be displayed on the 24-hour Sensor Glucose Overview Graph, any potential therapy decisions were made based on the incorrect…Straumann USA LLC recalls Emdogain
The possibility for this product that is intended for demonstration purposes only to be placed in patients.Argon Medical Devices, Inc recalls Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The…
Due to complaints of increased resistance when advancing the dilator within the introducer sheath.Mindray DS USA, Inc. dba Mindray North America recalls Sevoflurane and 1 more products
Potential for anesthesia leakage.Stryker Corporation recalls NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP and 2 more products
Tape used to secure components within packaging contains latex, despite products being labeled as latex-free.Cepheid recalls Xpert MTB/RIF. Model Number: GXMTB/RIF-US-10.
Product testing did not meet expected stability criteria.Foundation Medicine, Inc. recalls FoundationOne CDx and 1 more products
Reports were sent to customers without the companion diagnostic (CDx) Claims Page.Noah Medical Corporation recalls Brand Name: Galaxy System Product Name: Galaxy System Model/Catalog Number: GAL-001…
Due to Users not having access to the Instructions for Use/User Manual due to it being password protected.A little guidance
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