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Displaying 1 - 15 of 248 items.
Medfusion Syringe Infusion Pumps
Smiths Medical is issuing this letter to notify customers not to use Cardinal Health branded Monoject syringes with Medfusion 3500 and 4000 Syringe Pumps. On September 20, 2023, Cardinal Health issued a medical device product correction for the Cardinal…
RecallHealth product recall | 2024-03-14
Clip Applier
The recall was initiated due to an increase in clip applier complaints as the units form these lots have the potential to result in a clip not loading into the jaws after the trigger is actuated.
Recall Start Date: January 26, 2024
RecallHealth product recall | 2024-03-13
FOLIC ACID 1MG - Affected lots exceed or may exceed the acceptable intake limit for N-nitroso-folic acid.
Affected lots exceed or may exceed the acceptable intake limit for N-nitroso-folic acid.
RecallHealth product recall | 2024-03-12
Various Olympus Medical Endoscopes
As a result of catch up 510(k)s on the subject devices, the reprocessing instructions were changed. Specifically, the EtO gas mixture was revised to reflect the gas mixture that is commercially available and optionable reusable brushes were removed as a…
RecallHealth product recall | 2024-03-12
APO-MOMETASONE : Affected lots may contain the presence of bacterial contamination.
The affected lots may contain the presence of bacterial contamination.
RecallHealth product recall | 2024-02-19
VitalBulk : Product contains level of nicotinic acid found in prescription drugs
Product contain level of nicotinic acid found in prescription drugs. Product was imported and distributed without an establishment licence and market authorization.
RecallHealth product recall | 2024-02-09
TEVA-DILTIAZEM XC: Out of specification
The recall is due to an out of specification for TEVA-DILTIAZEM XC 360MG TAB 100 bottle dissolution result during stability testing.
RecallHealth product recall | 2024-02-07
Alma TED
Alma TED is not approved in Canada for hair restoration.
Recall Start Date: January 14, 2024
RecallHealth product recall | 2024-02-02
JAMP TELMISARTAN-HCT: Affected lots may contain higher dosage than the labelled dose
Possible presence of tablets containing only the hydrochlorothiazide layer in the affected lot which may also result in a higher dosage than the labelled dose of 12.5 mg.
RecallHealth product recall | 2024-01-24
Ferrous Fumarate 300 mg: Out of Specification
The total combined yeasts and molds count and/or the dissolution may be out of specification for the affected lots.
RecallHealth product recall | 2024-01-23
Oxy2Mask
There is a potential for the elbow component to not be securely connected to the diffuser component. This originated from a complaint received on November 15, 2023.
Recall start date: January 5, 2024
RecallHealth product recall | 2024-01-19
PEDIATRIX ORAL SOLUTION 100mg: Out of specification
The assay is out of specification for the affected lot.
RecallHealth product recall | 2024-01-15
Centricity High Acuity Anesthesia and Centricity Anesthesia
Patient allergies deleted from external systems are displayed in Centricity Critical Care (CCC), Centricity Anesthesia (CA), Centricity High Acuity Anesthesia (CHA-A) and Centricity High Acuity Critical Care (CHA-CC) products.
Recall Start Date:…
RecallHealth product recall | 2024-01-12
FlexiCups Medium Blue
Possibility of the blue elastomer cup crumbling or separating from the mandrel.
Recall Start Date: December 27, 2023
RecallHealth product recall | 2024-01-11
BBL Sensi-Disc Antimicrobial Susceptibility Test Discs
BD confirmed through a recent evaluation of BD BBL™ Sensi-Disc™ product that twenty-eight (28) out of thirty (30) antimicrobial discs showed reproducibility, accuracy, and/or quality control (qc) failures when tested with Haemophilus spp. Testing with…
RecallHealth product recall | 2024-01-10