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Cti Pet Systems Inc

Cti Pet Systems Inc Recalls

All product recalls associated with Cti Pet Systems Inc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 36661–36680 of 37661 recalls

Cti Pet Systems Inc: Siemens Models: BIOGRAPH, BIOGRAPH LSO and CTI Models: R...

CPS has found that in some instances, when the CT E-Stop is activated, a malfunction may occur where the PHS controller may not shut down and stop bed motion.

FDAOct 2, 2003Nationwide• Cti Pet Systems Inc

Heartport Inc Route: Introducer Sheath is indicated for patients requiring int...

Damaged hemostasis valves that prevent or present difficulty when inserting catheters.

FDAOct 2, 2003CA, FL, GA +17 more• Heartport Inc Route

Heartport Inc Route: EndoReturn arterial cannula. The EndoReturn arterial can...

Damaged hemostasis valves that prevent or present difficulty when inserting catheters.

FDAOct 2, 2003CA, FL, GA +17 more• Heartport Inc Route

1...1832 183318341835 1836...1884

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Heartport Inc Route: SoftClamp II arterial cannula is intended to deliver oxyg...

Damaged hemostasis valves that prevent or present difficulty when inserting catheters.

FDAOct 2, 2003CA, FL, GA +17 more• Heartport Inc Route

Heartport Inc Route: DirectFlow arterial cannula is intended to deliver oxygen...

Damaged hemostasis valves that prevent or present difficulty when inserting catheters.

FDAOct 2, 2003CA, FL, GA +17 more• Heartport Inc Route

Energizer Back-Up Power Supply – System Defect (2003)

Fire/Burn Risk

The recalled back-up power supply systems include the Energizer-brand UPS Model ER-PRO1000, which can be identified by a label on the back of the device. The black, breadbox-like unit is about 14 inches deep, 6 inches wide, 8 inches tall and weighs about 20 pounds. The words, "Energizer" and "energizerups.com" appear on the front of the unit.

CPSCOct 2, 2003Nationwide• Technuity Inc., of Indianapolis, Ind.

Merit Medical Systems, Inc: VacLok Syringe. Label reads in part: ''VACLOC SYRINGE 60...

There is a potential for the PETG blister trays to bond together with varying degrees of attachment. The potential for non-sterility exists when the attached trays are seperated by force and holes or cracks are generated in the seperated trays.

FDAOct 1, 2003Nationwide• Merit Medical Systems, Inc

Merit Medical Systems, Inc: IntelliSystem25 Inflation Device and Fluid Dispensing Syr...

FDAOct 1, 2003Nationwide• Merit Medical Systems, Inc

Merit Medical Systems, Inc: Waste Collection Kit. Label reads in part: ''CUSTOM KIT...

FDAOct 1, 2003Nationwide• Merit Medical Systems, Inc

Merit Medical Systems, Inc: Inflation Kit. Label reads in part: ''CUSTOM KIT...MERI...

FDAOct 1, 2003Nationwide• Merit Medical Systems, Inc

Merit Medical Systems, Inc: Monarch Inflation Device and Fluid Dispensing Syringe - L...

FDAOct 1, 2003Nationwide• Merit Medical Systems, Inc

Merit Medical Systems, Inc: Manifold Custom Kit. Label reads in part: ''CUSTOM KIT....

FDAOct 1, 2003Nationwide• Merit Medical Systems, Inc

Abbott Laboratories, Inc: AEROSET System Software version 1.02ER000

Audible alarm occurs before aspiration potentially resulting in operator injury or results assigned to wrong patient for STAT samples.

FDASep 30, 2003Nationwide• Abbott Laboratories, Inc

Centerpulse Orthopedics, Inc: RETi-LOCK Cluster-Hole Acetabular Shells with Sealed Scre...

Compalints of acetabular shell disassociating with the bone.

FDASep 30, 2003CA, ID, IN +3 more• Centerpulse Orthopedics, Inc

Boston Scientific: PeriVac brand Pericardial Fluid Aspiration Procedure Kit ...

The product has the potential to break during withdrawal process.

FDASep 29, 2003CA, CO, IL +11 more• Boston Scientific

Beckman Coulter Inc: Synchron CX4, CX5 and CX9 Pro Systems.

Motor driver boards may contain wrong type of microchip which does not have obstruction detection feature.

FDASep 29, 2003Nationwide• Beckman Coulter Inc

Segway i Series Transporter – Software Upgrade (2003)

This recall involves all Segway HT i167 ("i Series") models sold to consumers. In addition, Segway LLC is including all e167 ("e Series") and i167 models sold to commercial users, and all p133 ("p Series") models sold to consumers in test markets.

CPSCSep 26, 2003Nationwide• Segway LLC, of Manchester, New Hampshire

Misys Healthcare Systems: Calculator/ Data Processing Module for Clinical Use.

Software Defect. When orders are modified before the Roche Cobas Integra query for a specimen, the sample ID locks.

FDASep 25, 2003Nationwide• Misys Healthcare Systems

Eddie Bauer Propane Lantern (Wenzel) – Ignition Risk (2003)

The Eddie Bauer lantern, sold exclusively at Target stores, is ocean blue with two mantles. It has a glass globe, electronic ignition, and an extra-large hood and handle. When assembled, the lantern sits on a plastic base that houses the propane fuel cylinder. The "Eddie Bauer" name appears on the front of the product on an oval panel immediately below a black on/off switch. The Wenzel Company produces the lantern under license with Eddie Bauer.

CPSCSep 25, 2003Nationwide• The Wenzel Co., of St. Louis, Mo.

Bunk Beds (Home Line) – Safety Hazard (2003)

The recalled Home Line bunk beds include the following models and styles: S130 (black), S131 (white), S132 (red), and S133 (blue) have a single top mattress and a double width bottom mattress; S135 (black) and S136 (white) that have a single top and a single bottom mattress; and S116 (black) and S117 (white) that have a single top mattress and a bottom mattress that also converts into a couch. Some units are labeled with the "Home Line" name and the model numbers on the top front railing.

CPSCSep 25, 2003Nationwide• Home Line Industries, of Philadelphia, Pa.