2009 Product Recalls
1,443 recalls issued in 2009.
Showing 1441–1443 of 1,443 recalls
HARNESS ADJUSTER COVER/SHARP EDGES
THE SHARP EDGE OF THE FLASH COULD CAUSE CUTS, SCRATCHES, OR ABRASIONS ON THE FEET OR LEGS OF BARE-FOOTED INFANTS.
PEG PEREGO WILL NOTIFY REGISTERED OWNERS AND PROVIDE A FREE REPAIR KIT. THIS SAFETY CAMPAIGN BEGAN DURING APRIL 2008. OWNERS MAY CONTACT PEG PEREGO TOLL-FREE AT 1-888-734-6030.
Zimmer Metasul Head 32/-4'S', taper 12/14, hip implant component; REF 19.32.05.
The wrong part may be in the package. Package may contain a 28 mm head.
Zimmer notified consignees via recall letter dated 6/20/08 to return the product.
MassTRANSIT Infusion Catheter Kit, 605-731K & 605-780K, Cordis Neurovascular Intended to be used as a mechanism for the infusion of various diagnostic, embolic, and therapeutic agents into the Neurovascular, Peripheral Vascular and Coronary Vascular systems and for superselective angiography of peripheral and coronary vasculature.
Two lots of Cordis Neurovascular Masstransit Infusion Catheter Kits has the potential for sterile PTFE contamination within the inner lumen of the catheter.
A Medical Device Recall letter, dated 6/30/2008, and Acknowledgement Form were sent overnight. The firm asked customers to set aside any affected product in a manner that ensures it will not be used. Customers are asked to review, sign and return the enclosed Acknowledgement Form directly to Cordis Neurovascular. Customers can either return any product with reference to the RA# on the form, or contact their local sales reps to facilitate return of the affected product. Customers will receive a credit for the units they return. If any affected product has been forwarded to another facility, the facility should be contacted to arrange return of the product. If there are any additional questions, Customer Service may be also be contacted at 800-551-7683.