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Xiros Plc 28-30 Blenheim Terrace Leeds United Kingdom

Xiros Plc 28-30 Blenheim Terrace Leeds United Kingdom Recalls

All product recalls associated with Xiros Plc 28-30 Blenheim Terrace Leeds United Kingdom.

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Recall Summary

Total Recalls

1000

Past Year

567

Class I (Serious)

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 6921–6940 of 7756 recalls

Xiros Plc 28-30 Blenheim Terrace Leeds United Kingdom: Neoligaments Staple Impactor, 8 mm Staple Impactor: 202-3010

The impactors are being recalled for modification so that they can be disassembled fully for cleaning and sterilization, on suspicion that the assembled items retain contamination after cleaning and may not be effectively sterilized by the recommended hospital sterilization cycles.

FDAMay 17, 2006Nationwide• Xiros Plc 28-30 Blenheim Terrace Leeds United Kingdom

Xiros Plc 28-30 Blenheim Terrace Leeds United Kingdom: Neoligaments Staple Impactor, 6 mm Staple Impactor: 202-3001

FDAMay 17, 2006Nationwide• Xiros Plc 28-30 Blenheim Terrace Leeds United Kingdom

Gambro Renal Products, Inc.: Gambro Prismaflex Hemodialysis Machine, Catalogue Number ...

1...345 346347348 349...388

Page 347 of 388Next

A potential risk of infusing air or infusion fluid to the patient during dialysis. Also, a possibility of an incorrect scale reading of the amount of patient fluid removal.

FDAMay 16, 2006Nationwide• Gambro Renal Products, Inc.

Boston Scientific Cupertino, Corporation: NexStent Monorail Carotid Stent System, Material number M...

Tip may detach from stent delivery system.

FDAMay 15, 2006Nationwide• Boston Scientific Cupertino, Corporation

Beckman Coulter Inc: UniCel DxC 600/600PRO/600i/800/800PRO Synchron Clinical S...

Incorrect Reagent Status-When a new cartridge of Infinity Lithium Reagent is loaded on to the UniCel DxC System, the Reagent Status screen will incorrectly show 'Days Left' as 21. The correct Reagent Status for a new Lithium reagent cartridge is 14 days. Lithium reagent used past 14 days may produce low quality control and/or patient results.

FDAMay 15, 2006Nationwide• Beckman Coulter Inc

Gambro Renal Products, Inc.: Gambro Phoenix Hemodialysis Machine, Model numbers: 60229...

Defective Heat Exchanger/membrane; this may result in perforation of the membrane thus allowing the presence of infectious organisms and/or pathogens to pass from patient to patient.

FDAMay 12, 2006GA, IN, NC +1 more• Gambro Renal Products, Inc.

Hebron International, Inc.: Soft Cosmetic Contact Lenses sold under the brand names: ...

Contact lenses were distributed and sold to inappropriate retail establishments without professional eye care involvement.

FDAMay 10, 2006Nationwide• Hebron International, Inc.

Blackstone Medical, Inc.: Hallmark Anterior Cervical Plate System: Primary Bone Scr...

Incomplete Design Validation: the laser marking on the head of the screw lacked complete process qualification

FDAMay 8, 2006Nationwide• Blackstone Medical, Inc.

Spacelabs Medical Incorporated: Spacelabs Medical 1400 MHz Telemetry System,. Model 91341...

Potential for patient waveforms to move to an open receiver module or to an occupied receiver causing the intermittent inappropriate monitoring of both patients for several minutes.

FDAMay 5, 2006Nationwide• Spacelabs Medical Incorporated

Anthem Bicycle Helmets (Trek) – Impact Standard Failure (2006)

The recalled helmets are identified by the model name Anthem C Elite and Anthem C Elite WSD. A label inside the helmet identifies the helmet as "Trek Anthem C." The helmets are available in men's sizes in black/charcoal, blue/silver and blue/red, and in women's sizes in aqua blue/silver and white/silver. This recall includes all sizes of this helmet.

CPSCMay 4, 2006Nationwide• Trek Bicycle, of Waterloo, Wis.

ONELINK Smoke Alarms (First Alert) – Battery Drain (2006)

Fire/Burn Risk

The recall involves ONELINK™ battery-powered smoke and combination smoke/CO alarms. "First Alert" and "ONELINK™" are printed on the front of the alarm. The model number and date code are printed on the back of the alarm. Model number SA500 or SCO500 with a date code prior to March 3, 2006 are included in this recall.

CPSCMay 2, 2006Nationwide• BRK Brands Inc., a subsidiary of First Alert Inc., of Aurora, Ill.

Nicolet Biomedical Div of Viasys Healthcare: VIASYS Healthcare Disposable Bar Electrodes. Re-order No...

The Bar Electrodes do not meet performance specification for electrode impedance. A manufacturing defect was discovered in disposable bar electrodes, part number 019-435600, lot 604664, that has the potential to reduce the amplitude of a motor or sensory nerve action potential. These possible lower amplitudes will be measured only if the bar electrode is used as a bar.

FDAApr 28, 2006AL, CA, CT +6 more• Nicolet Biomedical Div of Viasys Healthcare

Boston Scientific Target: Boston Scientific brand Pivot Steerable Microcatheter, 1....

During forward advancement, the user may experience increased resistance and may exhibit jump-effect, and this could result in increase in procedure time, or vessel injury, including perforation.

FDAApr 26, 2006IN, OR• Boston Scientific Target

Southmedic Inc Po Box 1365 Barrie Canada Ontario: Vapofils with Stainless Steel Block Ends, Item Number V05...

Southmedic has initiated this recall because their Japanese distributor received field reports of leaking vapofils. Leakage may cause non-toxic spills in the hospital environment, distraction of practitioners during conduct of anesthesia and surgery, and may damage certain plastic equipment. Leakage may also expose patients to low concentrations of volatile anesthetics.

FDAApr 21, 2006FL, IN, NJ• Southmedic Inc Po Box 1365 Barrie Canada Ontario

Emergency Smoke Hoods (EVAC) – Carbon Monoxide Risk (2006)

Fire/Burn Risk

These smoke hoods are one-time use respiratory devices that assist users with breathing, while escaping a fire. They include a transparent plastic hood that covers the user's head, and a canister that filters out toxic gases. "EVAC+™" or "EVAC-U8™" is printed on the canister.

CPSCApr 20, 2006Nationwide• Brookdale International Systems Inc., of Vancouver, British Columbia, Canada

Hollister Stier Laboratories LLC: Sterile empty vials, 10mL/20mm closure sold 25/case. Lab...

Potential for vials to be cracked at the vial stopper interface. This could compromise the sterility of the products compounded into the vials.

FDAApr 20, 2006Nationwide• Hollister Stier Laboratories LLC

Beckman Coulter Inc: Coulter LH500 Hematology Analyzer: Part Numbers 178832, 1...

Beckman has confirmed that erroneous results could be reported when the workstation database crashes.

FDAApr 17, 2006Nationwide• Beckman Coulter Inc

Abbott Laboratories: CELL-DYN Sapphire and CELL-DYN 4000 Diluent/Sheath System...

High platelet background count when using the CELL-DYN 4000 System and/or CELL-DYN Sapphire System; with patient results unacceptable -out-of-range.

FDAApr 17, 2006AL, AR, CA +38 more• Abbott Laboratories

Beckman Coulter Inc: Access Immunoassay system CEA, in vitro diagnostic, Part ...

Firm has confirmed that the Access CEA Assay may generate decreased values with certain frozen platelet specimens.

FDAApr 12, 2006Nationwide• Beckman Coulter Inc

Bard Access Systems, Inc: 20F Tri-Funnel Replacement Gastrostomy Tube

Packaging for some gastrostomy tubes was labeled with incorrect balloon inflation data. An underinflated balloon may cause misplacement, slippage or premature removal of the tube. If an underinflated balloon allows the tube to be placed, or slip into, the stomal tract and not the stomach, there is a risk of infusion of fluids into the peritoneum. This carries the risk of infection.

FDAApr 6, 2006Nationwide• Bard Access Systems, Inc