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Bio-Logic Systems Corp

Bio-Logic Systems Corp Recalls

All product recalls associated with Bio-Logic Systems Corp.

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Recall Summary

Total Recalls

1000

Past Year

1000

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 18881–18900 of 21319 recalls

Bio-Logic Systems Corp: Bio-logic-Ceegraph/Sleepscan Netlink Traveler, Bio-logic ...

Battery and Battery Compartment; incorrect placement in the Netlink Traveler unit which caused a short in the wiring of the battery pack and overheating.

FDAFeb 26, 2007Nationwide• Bio-Logic Systems Corp

American Medical Systems: AMS DURA-II Universal Tips, 2cm, Product Number 72009361,...

Mis-Labeling:The Dura-II 2 cm Universal Tips and the Dura-II 4 cm Distal Tips were incorrectly labeled with the opposite labels.

FDAFeb 19, 2007Nationwide• American Medical Systems

American Medical Systems: AMS DURA-II Distal Tips, 4 cm, Product Number 72009340, S...

Mis-labeling: The Dura-II 2 cm Universal Tips and the Dura-II 4 cm Distal Tips were incorrectly labeled with the opposite labels.

FDA

1...943 944945946 947...1066

Page 945 of 1066Next

Feb 19, 2007

Nationwide

• American Medical Systems

Becton Dickinson & Co.: BD Sensi-Disc Ticarcillin TIC-75, in vitro diagnostic, ca...

Antibiotic susceptibility testing reagent was not manufactured according to specifications and may cause ineffective treatment regimen in patients with infections. The recalling firm received customer reports of false susceptibility results.

FDAFeb 19, 2007Nationwide• Becton Dickinson & Co.

General Electric Medical Systems Information Technology: GE Medical Systems Mac-Lab System, cardiac catheterizatio...

GE Healthcare has identified conditions that could cause a potential loss of real-time monitoring with the CardioLab/Mac-Lab/ComboLab Electrophysiology and Hemodynamic Monitoring Systems. These issues are associated with an audio driver, and the use of the application's log and imaging windows.

FDAFeb 16, 2007PR• General Electric Medical Systems Information Technology

General Electric Medical Systems Information Technology: GE Medical Systems CardioLab System, electrophysiological...

FDAFeb 16, 2007PR• General Electric Medical Systems Information Technology

General Electric Medical Systems Information Technology: GE Healthcare Systems ComboLab System. Made up of both M...

FDAFeb 16, 2007PR• General Electric Medical Systems Information Technology

Merit Medical Systems, Inc: StayFix Fixation Device for Percutaneous catheters, REF 6...

Sterility of some units may be compromised due to damaged packaging.

FDAFeb 15, 2007Nationwide• Merit Medical Systems, Inc

Merit Medical Systems, Inc: EpiFix Fixation Device for Epidural Catheters, REF 670M, ...

Sterility of some units may be compromised due to damaged packaging.

FDAFeb 15, 2007Nationwide• Merit Medical Systems, Inc

Inverness Medical Professional Diagnostics: Clearview Simplify D-dimer, in vitro diagnostic for quali...

Laceration Risk

Lot PX018A is exhibiting a decrease in sensitivity affecting the qualitative result around the cut off.

FDAFeb 15, 2007PR• Inverness Medical Professional Diagnostics

Becton Dickinson & Company: BD 30ml Syringe Luer-Lok tip Sterile BD, Franklin Lakes, ...

The unit label on a limited number of syringes is incorrect, citing a 20 ml size. All other levels of labeling are correct, identifying the product as 30 ml size.

FDAFeb 15, 2007Nationwide• Becton Dickinson & Company

Stentor Inc A Phillips Medical Systems Co.: The iSight PACS (picture archiving and communications sys...

A defect may cause patient image orientation markers to be incorrectly labeled on Multi-Planar Reformation (MPR) images. Left and Right Anatomical orientation markers may be reversed.

FDAFeb 14, 2007Nationwide• Stentor Inc A Phillips Medical Systems Co.

Orthopedic Systems Inc: Doro Products Adapter, Product number 5979-300. The adap...

Material used to manufacture accessory bracket does not meet product specification. The screw is normally composed of ''Torlon'', which is yellow. The part was made of "Tercite", which is blue.

FDAFeb 14, 2007Nationwide• Orthopedic Systems Inc

Battery Packs for Toy Vehicles (JAKKS Pacific) – fire risk (2007)

Fire/Burn Risk

This recall involves battery packs used with FLY WHEELS XPV toy vehicles. The battery packs were sold with a charger (item number 73904) and with the radio-controlled XPV toy (item number 73906). Item numbers are printed on the product's packaging above the barcode label. The batteries are marked "Fly Wheelz," "XPV," and "JAKKS Pacific," "Lithium-ion Polymer battery (LiPo)" followed by a list of warnings and precautions. The XPV Xtreme Performance Vehicle is not the subject of this exchange program.

CPSCFeb 13, 2007Nationwide• JAKKS Pacific Inc., of Malibu, Calif.

Stryker Howmedica Osteonics Corp.: Triathlon MIS 4:1 Cutting Blocks - Size 1-8; Catalog Numb...

Laceration Risk

Triathlon Cutting Blocks did not assemble to the Triathlon Impactor/Extractor Handle.

FDAFeb 12, 2007Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Triathlon AR 4:1 Cutting Blocks - Size 1-8; Catalog Numbe...

Laceration Risk

Triathlon Cutting Blocks did not assemble to the Triathlon Impactor/Extractor Handle.

FDAFeb 12, 2007Nationwide• Stryker Howmedica Osteonics Corp.

Atmel Microcontrollers (Atmel) – software upgrade (2007)

Fire/Burn Risk

The digital cellular communicator can be used as a primary means of security communications for a residence or business. The recall involves the Atmel microcontroller AT91SAM7S256 installed in Honeywell digital cellular communicator, Model 7845GSM.

CPSCFeb 12, 2007Nationwide• Atmel Corp., of San Jose, Calif. (microcontrollers)

GE OEC Medical Systems, Inc: OEC 9800MD Motorized C-arm System, Fluoroscopic X-ray Sys...

During routine service, a cover may have been installed without the required proper lead shielding.

FDAFeb 9, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC FluoroTrak Plus 9800 Fluoroscopic X-ray System,

During routine service, a cover may have been installed without the required proper lead shielding.

FDAFeb 9, 2007Nationwide• GE OEC Medical Systems, Inc

Digisonics, Inc: Doctors Review System, OB-Windows/OB-View software releas...

Study would on occasion have fetal heart rate and/or cervical length on the report that was not entered nor did it belong to that patient. Software displayed incorrect data for fetal heart rate and cervical length in OB ultrasound reports.

FDAFeb 9, 2007Nationwide• Digisonics, Inc