Fentanyl Citrate and Bupivacaine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
Pharmedium Services
Lack of sterility assurance.
95,075 total recalls in our database
Pharmedium Services
Lack of sterility assurance.
Pharmedium Services
Lack of sterility assurance.
American Pharmaceutical Ingredients
CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.
Pharmedium Services
Lack of sterility assurance.
American Pharmaceutical Ingredients
CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.
American Pharmaceutical Ingredients
CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.
Possible sterile barrier breach in the pouch of Affinity NT Cardiotomy Venous Reservoir stand alone uncoated and Affinity NT Cardiotomy Venous Reservoir stand alone Trillium coated products.
These finished good kits may contain the incorrect Springwire Guide (SWG).
Robot arm being sent to the wrong position
Arrow International
These finished good kits may contain the incorrect Springwire Guide (SWG).
After multiple reprocessing cycles, the epoxy resin which holds the TCN Electrode in the hub can exhibit signs of damage. In some cases, this damage may result in the inability to fully remove blood and/or tissue residuals prior to cleaning and re-sterilizing the device.
The product is labeled with the incorrect expiration date.
Arrow International
These finished good kits may contain the incorrect Springwire Guide (SWG).
Nine lots of 8.5 mm Polyaxial Pedicle Screws are at risk of breakage.
Allen Medical Systems
The base of the frame has the potential to crack when the patient is initially transferred to the Bow Frame.
Vygon MFG, Inc., dba/ Churchill Medical Systems
Vygon is conducting a voluntary recall of the products and lots listed in this recall, being initiated because our Tyvek supplier has notified Vygon of issues with their product, specifically the Tyvek may not be coated completely causing gaps in the adhesive used to seal the product packaging. This potential lack of adhesive may affect the sterility of the product.
The duodenoscopes are being recalled in order to replace the forceps elevator mechanism, the O-rings, and the distal end covering to be consistent with the updated design as well as provide an updated periodic inspection as part of the Operation Manual in order to mitigate the potential risk of infection in flexible endoscopy.
These finished good kits may contain the incorrect Springwire Guide (SWG).
Rapid fFN cassettes were manufactured with material (A137 ascites) from a new supplier (SDIX). The products were distributed to customers before FDA approved the change to use the material from SDIX.
Vygon MFG, Inc., dba/ Churchill Medical Systems
Vygon is conducting a voluntary recall of the products and lots listed in this recall, being initiated because our Tyvek supplier has notified Vygon of issues with their product, specifically the Tyvek may not be coated completely causing gaps in the adhesive used to seal the product packaging. This potential lack of adhesive may affect the sterility of the product.