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GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc Recalls

All product recalls associated with GE OEC Medical Systems, 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 33501–33520 of 37665 recalls

GE OEC Medical Systems, Inc: GEHC OEC 8800 Mobile Fluoroscopic X-ray System, GE Health...

X-ray units did not meet manufacturer's specification for linearity.

FDAOct 19, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: GEHC OEC 8800 Mobile Fluoroscopic X-ray System, GE Health...

X-ray units did not meet manufacturer's specification for linearity.

Class IIModerate

FDAOct 19, 2007Nationwide• GE OEC Medical Systems, Inc

Abbott Point of Care Inc.: Abbott Point of Care, i-STAT E3+ Cartridge, (NA K Hct); L...

Difficult to Close -- Certain lots of i-STAT cartridges are difficult to close, will not close or do not stay closed.

FDA

1...1674 167516761677 1678...1884

Page 1676 of 1884Next

Oct 18, 2007

Nationwide

• Abbott Point of Care Inc.

Abbott Point of Care Inc.: Abbott Point of Care, i-STAT EC4+ Cartridge; (NA K Glu Hc...

Difficult to Close -- Certain lots of i-STAT cartridges are difficult to close, will not close or do not stay closed.

FDAOct 18, 2007Nationwide• Abbott Point of Care Inc.

Abbott Point of Care Inc.: Abbott Point of Care, i-STAT 6+ Cartridge (Na K CL BUN/Ur...

Difficult to Close -- Certian lots of i-STAT cartridges are difficult to close, will not close or do not stay closed.

FDAOct 18, 2007Nationwide• Abbott Point of Care Inc.

Toy Pirate Swords (Gymboree) – Breakage Risk (2007)

Laceration Risk

This recall involves a toy pirate sword with SKU number 140025491-GYS049. The SKU number is printed on the price tag above the bar code. The sword is made of plastic, and has a gold-colored handle and a gray plastic blade. The sword is about 19 inches long.

CPSCOct 18, 2007Nationwide• The Gymboree Corp., of San Francisco, Calif.

Girls' Boots (Payless) – Fall Hazard (2007)

This recall involves black jeweled girls' boots. The boots have a silhouette of a guitar on the outer leg and a guitar-shaped zipper pull on the inner leg. "Hannah Montana" is engraved on the boot outsole and a photo of the singer and show's character is printed on the box. The boots were sold in girls' sizes 10½ to 4½. No other styles or models are involved in this recall.

CPSCOct 18, 2007Nationwide• Payless ShoeSource Inc., of Topeka, KS

GE OEC Medical Systems, Inc: GE OEC, Insta Trak 3500 Plus with the Cranial Application...

Crack, Fracture or Detachment: The Transmitter Arm for the Mayfield-compatible Transmitter may become detached from the unit and enter into the surgical field.

FDAOct 18, 2007AL, AZ, AR +22 more• GE OEC Medical Systems, Inc

Abbott Point of Care Inc.: Abbott Point of Care, i-STAT CREA Cartridge (Creatine/Cre...

Difficult to Close -- Certain lots of i-STAT cartridges are difficult to close, will not close or do not stay closed.

FDAOct 18, 2007Nationwide• Abbott Point of Care Inc.

Abbott Point of Care Inc.: Abbott Point of Care, i-STAT G Cartridge; (Glucose/Glu); ...

Difficult to Close -- Certain lots of i-STAT cartridges are difficult to close, will not close or do not stay closed.

FDAOct 18, 2007Nationwide• Abbott Point of Care Inc.

Tabletop Puppet Theaters (Guidecraft) – Lead Paint Violation (2007)

The recalled puppet theater has red panels on the front and sides and a chalkboard signboard on top. The puppet theater measures about 24 inches in length, 6 inches in width and about 28 inches in height.

CPSCOct 17, 2007Nationwide• Guidecraft Inc., of Englewood, N.J.

Beckman Coulter Inc: Access Power Supply Assembly Sled Part Number: A48196/684...

Electrical grounding failure: During manufacturing, internal testing found one instrument wlth an intermittent failure of the electrical grounding. The source of the problem was traced to inadequate soldering.

FDAOct 17, 2007Nationwide• Beckman Coulter Inc

Skull Pails (R.L. Albert) – Lead Paint Violation (2007)

This recall involves the Albert's Halloween skull pails filled with candy mix. The skull-shaped pail is white with green eyes, nose and teeth. The pail has a clear lid with a label in which "Albert's" and "Skull Pails Filled with Halloween Candy Mix" is printed. The pail measures about 5 ½ inches high.

CPSCOct 17, 2007Nationwide• R.L. Albert & Son, of Greenwich, Conn.

PZ50 Snowmobiles (Yamaha) – Steering Danger (2007)

This recall involves all model year 2007 PZ50 snowmobiles, including PZ50W (Phazer), PZ50FXW (Phazer FX), PZ50GTW (Phazer GT), PZ50MW (Phazer Mountain Lite), and PZ50VTW (Venture Lite) model snowmobiles.

CPSCOct 16, 2007Nationwide• Yamaha Motor Corporation U.S.A., of Cypress, Calif.

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Sprint Fidelis 6948 Steroid eluting, quadripola...

Medtronic Cardiac Rhythm Disease Management has voluntarily suspended worldwide distribution of the Sprint Fidelis family of defibrillation leads because of the potential for lead fractures. In addition, the company recommends against new implants of the leads (Sprint Fidelis Models: 6930, 6931, 6948, 6949). Medtronic, its Independent Physician Quality Panel, and Bruce Lindsay, M.D., Professor of

FDAOct 15, 2007PR• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Sprint Fidelis 6930 Steroid eluting, tripolar, ...

FDAOct 15, 2007PR• Medtronic Inc. Cardiac Rhythm Managment

Interpore Cross International Inc: Allogenix; DBM in a Lipid Carrier with Calcium Granules; ...

Unapproved Testing: Interpore Cross International was recently informed that one of its human tissue suppliers, LifeLink Tissue Bank ("LifeLink"), utilized unapproved diagnostic testing (HBsAg & HBc) on certain lots of distributed donor tissue instead of the FDA approved screening test. As a result, Interpore Cross International has initiated a recall on specific lots of products containing human

FDAOct 15, 2007Nationwide• Interpore Cross International Inc

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Sprint Fidelis 6931 Steroid eluting, tripolar, ...

FDAOct 15, 2007PR• Medtronic Inc. Cardiac Rhythm Managment

Interpore Cross International Inc: InterGro PLUS; DBM in a Lipid Carrier with Calcium Granu...

Unapproved Testing:Interpore Cross International was recently informed that one of its human tissue suppliers, LifeLink Tissue Bank ("LifeLink"), utilized unapproved diagnostic testing (HBsAg & HBc) on certain lots of distributed donor tissue instead of the FDA approved screening test. As a result, Interpore Cross International has initiated a recall on specific lots of products containing human

FDAOct 15, 2007Nationwide• Interpore Cross International Inc

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Sprint Fidelis 6949 Steroid eluting, quadripola...

FDAOct 15, 2007PR• Medtronic Inc. Cardiac Rhythm Managment