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Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany

Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany Recalls

All product recalls associated with Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany.

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Recall Summary

Total Recalls

1000

Past Year

731

Class I (Serious)

175

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 10101–10120 of 11123 recalls

Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany: VectorVision (VV) Sky Navigation Platform (19" Computer R...

Diameter of cables used for installation are to small for the applied current. If an internal short circuit is produced the medical power supply will not shut down automatically and will continue to deliver current, which could result in overheating cables.

FDANov 12, 2007Nationwide• Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany

Medtronic Sofamor Danek USA Inc: Medtronic Sofamor Danek USA, CD Horizon Spinal System Agi...

Breaks: Shear failure of the cable component of the system.

FDANov 12, 2007Nationwide• Medtronic Sofamor Danek USA Inc

Curious George Plush Dolls (Marvel) – Lead Exposure (2007)

Fire/Burn Risk

This recall involves Curious George 12-inch plush dolls with a plastic face. The dolls are dressed to represent five various themes: birthday, fireman, sweet dreams, tool time and tool time with a soft face. The plush dolls were sold with a Curious George storybook or activity book. The following product and SKU numbers are printed on the packaging. Birthday 90253/ 8-83199-90253-5 Fireman 90246/ 8-83199-90246-7 Sweet Dreams 90247/ 8-83199-90247-4 Tool Time 90251/ 8-83199-90251-1 Tool Time (soft face) 90251/ 8-83199-90251-1

1...504 505506507 508...557

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CPSCNov 8, 2007Nationwide• Marvel Toys, of New York, N.Y.

Parks Medical Electronics Inc: Parks Medical Ultrasonic Doppler Flow Detector, Model 811...

Premature battery failure: Wrong acid flux used on circuit board which may lead to premature battery failure of ultrasonic non-directional doppler flowmeter.

FDANov 8, 2007Nationwide• Parks Medical Electronics Inc

Parks Medical Electronics Inc: Parks Medical Dual Frequency Doppler Vascular Flow Detect...

Premature battery failure: Wrong acid flux used on circuit board which may lead to premature battery failure of ultrasonic non-directional doppler flowmeter.

FDANov 8, 2007Nationwide• Parks Medical Electronics Inc

Stryker Medical Div. of Stryker Corporation: Stryker inTouch Critical Care bed; Model 2130, Stryker Me...

Multiple defects: 1) beds exhibit reverse motions when the Fowler, gatch or foot section is activated 2) a battery charging defect which may result in a depletion of battery power 3) the touch screen on the footboard freezing, resulting in controls to powered, pressure-relief mattresses being difficult to access 4) beds equipped with zoom drive systems may have an overdrive problem which could re

FDANov 2, 2007Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Howmedica Osteonics Corp.: Stryker LFIT COCR V40 Femoral Head; xx-Long (+16mm) Neck ...

Fracture of Stem Neck - The firm recently performed laboratory testing indicates that there may be a potential increased risk of stem neck fractures when a V40 +16mm offset femoral head is mated with certain Accolade TMZF femoral stems in patients classified as overweight or obese.

FDANov 2, 2007Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Medical Div. of Stryker Corporation: Stryker inTouch Zoom Critical Care bed, Model 2140, Stryk...

FDANov 2, 2007Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Howmedica Osteonics Corp.: Stryker Trial Head xx-Long (+16mm) Neck Length 26mm Diame...

FDANov 2, 2007Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Stryker COCR V40 Femoral Head; xx-Long (+16mm) Neck Lengt...

FDANov 2, 2007Nationwide• Stryker Howmedica Osteonics Corp.

C9600 Digital Color Printers (Oki) – Electrical Shock (2007)

The digital color printers are beige colored and measure 27 inches wide, 25 inches deep and 20 inches high. "Oki Printing Solutions" and model "C9600" are printed on the front of the unit. The following serial numbers are included in the recall. The serial number is located on the back left side of the printer. Serial Numbers AA56002655A0 through AA56002804A0 AA58001468A0 through AA58001617A0 AA58002702A0 through AA58002801A0

CPSCOct 30, 2007Nationwide• Oki Data Corporation, of Japan

Stryker Howmedica Osteonics Corp.: UStryker Orthopaedics; HR Universal Bipolar Component; 26...

Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head.

FDAOct 26, 2007Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Stryker Orthopaedics, UHR Universal Bipolar Component; 26...

Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head.

FDAOct 26, 2007Nationwide• Stryker Howmedica Osteonics Corp.

Football Bobble Head Cake Decorations (DecoPac) – Lead Paint (2007)

The recall includes plastic miniature football bobble heads with green bases only, which were sold for placement on a cake. The bobble heads represented the following teams: Baltimore Ravens, Green Bay Packers, Oakland Raiders, Chicago Bears, Indianapolis Colts, Philadelphia Eagles, Cincinnati Bengals, New England Patriots, Pittsburgh Steelers, Dallas Cowboys, New Orleans Saints, San Francisco 49ers, Denver Broncos, New York Giants, St. Louis Rams. Football bobble heads with black bases are not included in this recall.

CPSCOct 25, 2007Nationwide• DecoPac Inc., of Anoka, Minn.

Beckman Coulter Inc: SYNCHRON Systems Salicylate (SALY) Reagent; Part Number: ...

The Salicylate Reagent lots listed here may fail calibration and/or fail to maintain linearity at the upper end of analytical range.

FDAOct 22, 2007Nationwide• Beckman Coulter Inc

ARKRAY USA INC.: Hypoguard Advance Micro-draw Blood Glucose Monitoring Sys...

Mis-labeled/coded strips : Meter kits from this lot contain mislabeled 10-count test strip vials. The code number printed on the Advance Micro-draw 10-count test strip bottle is incorrect. The code number on the vial is 867 when it should be 687. The 687-labeled code chip contains the correct calibration information for the "867" test strips, so the meter will function properly and give accurat

FDAOct 18, 2007Nationwide• ARKRAY USA INC.

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

Gas Regulators (Fisher Controls) – Leak Hazard (2007)

Fire/Burn Risk

The recalled gas regulators were manufactured from March 2007 through May 2007 and installed on natural gas or LP-gas supply systems in homes and small commercial buildings. The recalls involves model HSR natural gas regulators and LP-gas regulators with model numbers 67CD, 67CH, 67CN, and 67CW, HSRL, R622, R622E, R622H, R632, R642, R652, R652E, R122H, R222, or R232. The model number can be found on a white label attached to the regulator spring case. The date of manufacture is also stamped on the regulator.

CPSCOct 12, 2007Nationwide• Fisher Controls International (FCI), of McKinney, Texas

Beckman Coulter Inc: Cytomics FC 500 Flow Cytometry System with CXP Software V...

Software error: This field action was initiated after Beckman Coulter determined that the CXP software does not refresh the dataset automatically under certain circumstances. The User documentation does not clearly state that the user should refresh the dataset after changes are made.

FDAOct 11, 2007Nationwide• Beckman Coulter Inc

Beckman Coulter Inc: Beckman Coulter UniCel Dxl 800 Access Immunoassay System;...

Incorrect results: There is an increased variance in assay performance when the UniCel Dxl 800 Modification (MOD ID 10027) and/or UniCel Dxl 800 Modification (MOD ID 6733) have been implemented and there are room fluctuations after assay calibration between the extremes of the 18C and 32C operating range.

FDAOct 8, 2007Nationwide• Beckman Coulter Inc