Ross Products Division Abbott Laboratories Recalls

FDA
5
Total Recalls
1
Agencies
Oct 2008
First Recall
Sep 2012
Latest Recall

Showing 1-5 of 5 recalls

FDA

The Companion ClearStar Pump System, for enteral feeding.

The transducer adapter bracket on the pump could crack or break and potentially result in under delivery of the enteral product.

Consignees were notified by letter dated 6/25/2007. A revised letter was sent 07/26/2007.

FDA

Embrace Enteral Pump

Continued use of the pump may cause the door pivot point on the back of the pump to crack or break. This will cause the pump to shut down and stop the initiation of enteral feeding.

Consignees were notified by letter dated 6/25/2007. The firm sent a revised letter on 07/26/2007.

FDA

Flexiflo Quantum Enteral Pump

Pumps were manufactured with an incorrect circuit board that may cause an increase in the feed rate and flush frequency of fluids.

The firm contacted all consignees via telephone and letter on 08/18/2004.

FDA

Patrol enteral pump set with piercing pin, list #520540.

The enteral pump set may have a 1-3 mm slit in the silicone tubing located between the blue connector and the stretch band Safe-T-Valve.

The recalling firm sent a recall letter dated April 27, 2007 to all customers.

FDA

Ross Hide-A-Port Low Profile Balloon Gastrostomy Tube Kit, 14 Fr., 0.8 cm length, Item Numbers: 53126 and 55602.

The balloons may be defective as indicated by an increased number of early balloon failures, which may result in tube displacement from patient.

The firm notified their customers on 3/1/2004 by telephone, fax, and FedEx. Product will be returned.