TY - JOUR
AU - 
AB - 39_BSS030409.qxd 2/3/09 10:27 PM Page 29 Biomedical Safety & Standards March 1, 2009 Site numbers for the 709 devices affected by b) GE Signa Excite 1.5T and 3.0T MR Systems, mod- this action are available from the firm, which began els 5107849, 5107849-2, M3000PT, and M3000PW the recall by letter on February 7, 2008. Loosening (Recall # Z-1891-2008). screws may cause the collimator to fall from the Codes are available from the firm, which document- x-ray stand. ed an artifact that could affect the diagnostic capability associated with the 3.0T Propeller T2 Flair application. Contact: Philips Medical Systems, North America Co., 22100 Bothell Everett Highway, Bothell, WA Contact: GE Healthcare, 3000 N. Grandview Boule- 98021-8431; Ph.: 425/487-7665. vard, Waukesha, WI 53188-1615; Ph.: 262/544-3894 . Obstetric Vacuum Temporary Pacing Systems and Parts Catheter Kits Cooper Surgical, Inc. (Trumbull, CT) recalled the Arrow International, Inc. (Asheboro, NC) recalled following products by letter on January 16, 2008: the following products by letter on April 11, 2008: a) M-Style Mushroom Cup Vacuum Assisted Delivery a) Arrow Balloon Temporary Pacing Catheter Kits, System used with hand pump, ref 10007LP part number AI-07155-KS (distributed in the (Recall # Z-1887-2008); U.S.), 5 Fr (110 cm) Pacing 
TI - Temporary Pacing Catheter Kits
JF - Biomedical Safety & Standards
DO - 10.1097/01.BMSAS.0000346132.54126.f4
DA - 2009-03-01
UR - https://www.deepdyve.com/lp/wolters-kluwer-health/temporary-pacing-catheter-kits-Tzubk0lFiu
SP - 29
EP - 29
VL - 39
IS - 4
DP - DeepDyve
ER -