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Bard Access Systems, Inc. alerts

Verified recalls, refunds, lawsuits, and settlements involving Bard Access Systems, Inc..

Recall Active FDA Official source

Bard Access Systems, Inc.: CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609...

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Product details:...

Company: Bard Access Systems, Inc.
Deadline: No deadline listed
Source: U.S. Food and Drug Administration

View affected products Official source

Recall Active FDA Official source

Bard Access Systems, Inc.: 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr...

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier. Product details: 5855240...

Company: Bard Access Systems, Inc.
Deadline: No deadline listed
Source: U.S. Food and Drug Administration

View affected products Official source