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Showing 61821–61840 of 68218 results

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Vital Signs Colorado Inc.: Light Wand Orotracheal Lighted Stylet, Part number: 3910....

Light protector may detach from lighted stylet during intubation.

FDAAug 11, 2008CA, GA, IN +9 more• Vital Signs Colorado Inc.

Siemens Medical Solutions USA, Inc: Coroskop Top X-Ray System, Model number 6134808.

Unintended movement of the system table and/or C arm.

FDAAug 11, 2008Nationwide• Siemens Medical Solutions USA, Inc

Ethicon, Inc. US: VICRYL RAPIDE (polyglactin 910) Braided Coated Synthetic ...

Package defect compromised the integrity of the primary seal, which could lead to premature suture degradation and/or impair the sterile barrier of the product.

FDAAug 11, 2008Nationwide• Ethicon, Inc. US

Siemens Medical Solutions USA, Inc: Bicor Hi-P X-Ray System, Model numbers 6379767 and 6258383.

Unintended movement of the system table and/or C arm.

FDAAug 11, 2008Nationwide• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc: BICOR POLYDOROS X-Ray System, Model number 6134667.

Unintended movement of the system table and/or C arm.

FDAAug 11, 2008Nationwide• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc: Coroskop X-Ray System, Model numbers 6258219 and 6379759.

Unintended movement of the system table and/or C arm.

FDAAug 11, 2008Nationwide• Siemens Medical Solutions USA, Inc

Nova Biomedical Corporation: Stat Profile Critical Care Xpress (CCX and CCX+), CCX Cre...

Erroneous, low creatinine results on CCX analyzer

FDAAug 11, 2008Nationwide• Nova Biomedical Corporation

Siemens Medical Solutions USA, Inc: BICOR TOP X-Ray System, Model number 6134816.

Unintended movement of the system table and/or C arm.

FDAAug 11, 2008Nationwide• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc: MULTISTAR D X-Ray System, Model number 3772501.

Unintended movement of the system table and/or C arm.

FDAAug 11, 2008Nationwide• Siemens Medical Solutions USA, Inc

Sterilmed Inc: Phaco Tips Model #'s: ALC30RTS ALC8065740806 ALC8065740...

SteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted because the possibility exists that some of the pouches were not properly sealed on one end. A breach in packaging seal or a failure in packaging integrity has the possibility of risk to the patient in terms of transmitting organisms capable

FDAAug 8, 2008AL, AZ, CA +33 more• Sterilmed Inc

Sterilmed Inc: Compression Sleeves Model #'s: HUNDVT10-1 and KEN5329 T...

SteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted because the possibility exists that some of the pouches were not properly sealed on one end. A breach in packaging seal or a failure in packaging integrity has the possibility of risk to the patient in terms of transmitting organisms capable

FDAAug 8, 2008AL, AZ, CA +33 more• Sterilmed Inc

Sterilmed Inc: Cardiac Imaging Catheter Model #'s: ACU08267996 and ACU5...

SteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted because the possibility exists that some of the pouches were not properly sealed on one end. A breach in packaging seal or a failure in packaging integrity has the possibility of risk to the patient in terms of transmitting organisms capable

FDAAug 8, 2008AL, AZ, CA +33 more• Sterilmed Inc

Sterilmed Inc: Tourniquet Cuffs Model #'s: INSDT-7024-02 INSDT-7218-01 ...

SteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted because the possibility exists that some of the pouches were not properly sealed on one end. A breach in packaging seal or a failure in packaging integrity has the possibility of risk to the patient in terms of transmitting organisms capable

FDAAug 8, 2008AL, AZ, CA +33 more• Sterilmed Inc

Sterilmed Inc: EP Cables Model #'s: BAR560004P BIOC10MR10MSTKS BIOC5-M...

SteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted because the possibility exists that some of the pouches were not properly sealed on one end. A breach in packaging seal or a failure in packaging integrity has the possibility of risk to the patient in terms of transmitting organisms capable

FDAAug 8, 2008AL, AZ, CA +33 more• Sterilmed Inc

Sterilmed Inc: Laser Probe Model #': SYN55.26.25 Reprocessed laser probe...

SteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted because the possibility exists that some of the pouches were not properly sealed on one end. A breach in packaging seal or a failure in packaging integrity has the possibility of risk to the patient in terms of transmitting organisms capable

FDAAug 8, 2008AL, AZ, CA +33 more• Sterilmed Inc

Sterilmed Inc: Biopsy Forceps, Cold Model #'s: BAR000386 BAR000388 MIC1...

SteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted because the possibility exists that some of the pouches were not properly sealed on one end. A breach in packaging seal or a failure in packaging integrity has the possibility of risk to the patient in terms of transmitting organisms capable

FDAAug 8, 2008AL, AZ, CA +33 more• Sterilmed Inc

Sterilmed Inc: Open & Unused Items - This refers to a sterilization serv...

SteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted because the possibility exists that some of the pouches were not properly sealed on one end. A breach in packaging seal or a failure in packaging integrity has the possibility of risk to the patient in terms of transmitting organisms capable

FDAAug 8, 2008AL, AZ, CA +33 more• Sterilmed Inc

Sterilmed Inc: Colorado Electrodes Model #'s: COLN104A COLN112A and ST...

SteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted because the possibility exists that some of the pouches were not properly sealed on one end. A breach in packaging seal or a failure in packaging integrity has the possibility of risk to the patient in terms of transmitting organisms capable

FDAAug 8, 2008AL, AZ, CA +33 more• Sterilmed Inc

Sterilmed Inc: Rasps Model #'s: KOMKM5100-37-113 KOMKM-82 STR1675-115 S...

SteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted because the possibility exists that some of the pouches were not properly sealed on one end. A breach in packaging seal or a failure in packaging integrity has the possibility of risk to the patient in terms of transmitting organisms capable

FDAAug 8, 2008AL, AZ, CA +33 more• Sterilmed Inc

Sterilmed Inc: Taps Model #'s: SYN311.15 SYN311.190 SYN311.39 and SYN31...

SteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted because the possibility exists that some of the pouches were not properly sealed on one end. A breach in packaging seal or a failure in packaging integrity has the possibility of risk to the patient in terms of transmitting organisms capable

FDAAug 8, 2008AL, AZ, CA +33 more• Sterilmed Inc

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