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Displaying 1 - 15 of 300 items.
Taro Pharmaceuticals Inc. is recalling all lots of Taro-Zoledronic acid injection 5mg/100mL (DIN 02415100) because they may contain particulate matter.
Zoledronic acid is a prescription drug used to treat and prevent osteoporosis and to treat Paget's…
RecallHealth product recall | 2022-08-10
Jamp Pharma Corporation is recalling one lot (MHC1403A) of Jamp-Atorvastatin 40 mg tablets due to possible contamination with latex pieces during manufacturing. A piece of latex was found in one tablet from the affected lot.…
RecallHealth product recall | 2022-08-08
Solution bags may be leaking in affected lot.
RecallHealth product recall | 2022-08-04
The affected lots may contain glass particles.
RecallHealth product recall | 2022-08-02
Abbott has identified that a subset of Assurity and/or Endurity pacemaker(s) are impacted by a manufacturing issue. As background, the issue in this recall is connected to a manufacturing laser roughening process, unique to a single assembly site…
RecallHealth product recall | 2022-08-02
Affected lot exceeds concentration limit for N-nitrosodimethylamine (NDMA).
RecallHealth product recall | 2022-07-28
Presence of Gluconacetobacter liquefaciens in affected lots.
RecallHealth product recall | 2022-07-25
A bug has been detected in the planning software. When loading images, there may be a left/right inversion. Display of image series is flipped after importing a sagittal oriented image series stored using the enhanced Dicom format.
Recall start date:…
RecallHealth product recall | 2022-07-18
Affected lot(s) may contain the presence of particulate matter.
RecallHealth product recall | 2022-07-15
Intuitive has become aware of the potential for unexpected motion caused due to partial disengagement of the instrument from the system while using the da vinci s/si and x/xi Endowrist clip applier instruments. Intuitive has received several complaints…
RecallHealth product recall | 2022-07-11
Smiths Medical implemented a design change in 2016 to widen the hinge assembly on the Level 1 H-2 Pressure Chambers used with the Level 1 Fast Flow Fluid Warmers (Models H-1025 or H-1200) or added to the H-1000 model. Smiths Medical has become aware that…
RecallHealth product recall | 2022-07-11
Medtronic is notifying health care professionals of the potential for reduced shock energy (~79% of programmed energy) during high-voltage (hv) therapy for Cobalt and Crome implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
RecallHealth product recall | 2022-07-04
Medtronic is informing customers of product performance issues related to the Heartware Ventricular Assist Device (HVAD) system batteries. Medtronic is taking actions to address two separate battery issues: 1) a weld nonconformance has been identified…
RecallHealth product recall | 2022-07-04
The sterility is out of specification in the affected lot (Periodic Media Fill Validation failure).
RecallHealth product recall | 2022-06-30
The products may contain undeclared ingredients which are listed on the Prescription Drug List.
RecallHealth product recall | 2022-06-21