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SagaTech Electronics, Inc.

SagaTech Electronics, Inc. Recalls

All product recalls associated with SagaTech Electronics, Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 32961–32980 of 37665 recalls

SagaTech Electronics, Inc.: Finger Sensor for Remmers Recorder (Formerly SnoreSat Sle...

The outer jacket is receding away from the black sensor prematurely.

FDAMay 8, 2008Nationwide• SagaTech Electronics, Inc.

Medtronic International Trade Inc: Medtronic Trillium AFFINITY NT, 511T, Hollow Fiber Oxygen...

Medtronic is advising that certain Trillium-coated Medtronic cardiopulmonary bypass (CBP) products (e.g., oxygenators, reservoirs, pumps and tubing packs) were manufactured with heparin batches contaminated with oversulfated chondroitin sulfate (OSCS). Based upon currently available information, Medtronic has determined that Medtronic Trillium-coated products can continue to be used in cardiopulm

FDAMay 7, 2008Nationwide• Medtronic International Trade Inc

GE Healthcare Integrated IT Solutions: GE Centricity PACS RA1000 Workstation; for diagnostic ima...

A software anomaly results in incorrect study date and time information being displayed in the report screen and title, which may result in a potential patient misdiagnosis.

1...1647 164816491650 1651...1884

Page 1649 of 1884Next

FDAMay 6, 2008Nationwide• GE Healthcare Integrated IT Solutions

Depuy Orthopaedics, Inc.: Depuy LCS Knee - Orthopedic knee implant. Meniscal beari...

Labeling Discrepancy -- Mislabeled and mis-etched as to size. Inserts were labeled and packaged as size Standard, 12.5mm Inserts but were actually a 10mm Inserts. Risks include but not limited to: a delay in the procedure while the proper component is located, and tight joint with constricted movement as a result of implantation of the wrong thickness of insert.

FDAMay 6, 2008Nationwide• Depuy Orthopaedics, Inc.

Playground Swing Sets (Playworld) – Fall Hazard (2008)

Swing sets involved in this recall have the following part numbers: 8 ft 2-Unit Standard Swing 0248 5 in Arch Swing w-8 ft Top Rail 0287 8 ft Standard Duty Swing Add-A-Bay 0230 5 in Arch Swing 2-Unit Add-A-Bay 0370 10 ft 2-Unit Standard Swing 0249 3-1/2 in Arch Swing w-8 ft Top Rail 0288 10 ft Standard Duty Swing Add-A-Bay 0231 3-1/2 in Arch Swing Add-A-Bay 0375 8 ft 2-Unit Heavy Duty Swing 0270 2-3/8 in Arch Swing w-7 ft Top Rail 0120 8 ft heavy duty swing add-a-bay 0232 2-3/8 in Arch Swing Add-A-Bay 0121 10 ft 2-Unit Heavy Duty Swing 0259 7 ft Early Childhood T-Swing 0290 10 ft Heavy Duty Swing Add-A- Bay 0233 8 ft Single Post Swing Assembly 0295 8 ft Single Post Swing Add-A- Bay 0296

CPSCMay 6, 2008Nationwide• Playworld Systems Inc., of Lewisburg, Pa.

Medical Device Technologies, Inc.: Hawkins III Breast Localization Needle. Product number 24...

The sterility of the product cannot be guaranteed.

FDAMay 6, 2008Nationwide• Medical Device Technologies, Inc.

Michigan Orthopaedic Products, Inc.: InterGro DBM Demineralized Bone Matrix in a lipid carrier...

Exposure to temperature extremes -- Product was not stored under controlled conditions and may have been temperature abused. Exposure to temperature extremes could cause problems with device safety (e.g. risk of infection) or problems with device effectiveness (e.g. lower healing rates if the factors or collagen in the device were affected by the temperature extremes).

FDAMay 5, 2008Nationwide• Michigan Orthopaedic Products, Inc.

Datex Ohmeda, Inc. dba GE Healthcare: Corometrics MODEL 250 Series Maternal/ Fetal Monitor, Mod...

Communication connector within monitor is defective and may cause potential loss of telemetry.

FDAMay 5, 2008Nationwide• Datex Ohmeda, Inc. dba GE Healthcare

Boston Scientific Corporation: iReview" Software (Accessory To) iLab Ultrasound Imaging ...

The firm initiated a recall of a specific iReview" Software, Ver 1.0 Kit, which was released for distribution in a non-validated format.

FDAMay 2, 2008AZ, CA, FL +3 more• Boston Scientific Corporation

GE Healthcare: GE Precision RXi Digital remote X-Ray Imaging R&F System,...

The Precision RXi collimator did not contain a label identifying the device as being certified to comply with applicable requirements of the x-ray performance standard.

FDAMay 1, 2008AK, CO, IL +15 more• GE Healthcare

GE Healthcare: GE Precision MPi, model 2385125. GE Medical Systems - Am...

The Precision MPi collimator did not contain a label identifying the device as being certified to comply with applicable requirements of the x-ray performance standard.

FDAMay 1, 2008CA, CO, FL +11 more• GE Healthcare

ThermoFisher Scientific Co., LLC: 10% Buffered Formalin Phosphate; Certified For laboratory...

Assay tests on retention sample of 10% Buffered Formalin Phosphate showed it to be 3.417%, which is below the specification of 4-5%.

FDAMay 1, 2008Nationwide• ThermoFisher Scientific Co., LLC

Dako North America Inc.: PT Link Waterbath, Model#PT100. Lab Vision PT Module Plu...

Dako is recalling the PT Link Waterbath because of a possible electrical hazard. Specifically, if the heater pad under the reagent tank becomes wet, it may present an electrical shock hazard when the lid is open.

FDAMay 1, 2008Nationwide• Dako North America Inc.

Philips Medical Systems (Cleveland) Inc: GEMINI PET/CT System, a diagnostic imaging system for fix...

The reason for this inspection is to determine if the Spindle Block Servo Controllers on the CT subsystem of potentially affected GEMINI PET/CT systems are susceptible to premature failure.

FDAMay 1, 2008AL, AZ, CA +32 more• Philips Medical Systems (Cleveland) Inc

GE Healthcare: Advantage Workstation version 4.2P, 4.3 and 4.4 with Volu...

GE Healthcare has recently became aware of a possible mismatch between the label of the tracked vessel and the underlying image associated with the cardio- vascular applications of the Advantage workstation that may impact patient safety.

FDAMay 1, 2008AL, AK, AZ +47 more• GE Healthcare

Stryker Communications Corp: Surgical Table Column Casing Revision B, Product #0788-2...

Potential exists for energy chain, which is responsible for protecting hydraulic and electrical cables during up and down motion on VERTIER Surgical Table, to become lodged between column case sections resulting in possible reduction or lose of function to hand and/or foot controls or possible involuntary movement of the table.

FDAMay 1, 2008Nationwide• Stryker Communications Corp

GE Healthcare: GE Precision MPi, model 5126893. GE Medical Systems - Am...

The Precision MPi collimator did not contain a label identifying the device as being certified to comply with applicable requirements of the x-ray performance standard.

FDAMay 1, 2008CA, CO, FL +11 more• GE Healthcare

Medtronic Neuromodulation: Medtronic Synchromed II Programmable Pump , Medtronic Inc...

SynchroMed II pumps (non-implanted) may have been manufactured without propellant.

FDAMay 1, 2008AL, AK, AZ +46 more• Medtronic Neuromodulation

Dako North America Inc.: PT Link Waterbath, Model#PT100. Lab Vision PT Module P...

Class IIModerate

FDAMay 1, 2008Nationwide• Dako North America Inc.

Philips Medical Systems (Cleveland) Inc: GEMINI PET/CT System, a diagnostic imaging system for fix...

The reason for this inspection is to determine if the Spindle Block Servo Controllers on the CT subsystem of potentially affected GEMINI PET/CT systems are susceptible to premature failure.

Class IIModerate

FDAMay 1, 2008AL, AZ, CA +32 more• Philips Medical Systems (Cleveland) Inc