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Microvision Medical Holding B.V. Meibergdreef 45 Amsterdam Netherlands

Microvision Medical Holding B.V. Meibergdreef 45 Amsterdam Netherlands Recalls

All product recalls associated with Microvision Medical Holding B.V. Meibergdreef 45 Amsterdam Netherlands.

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Recall Summary

Total Recalls

398

Past Year

Class I (Serious)

Most Recent

Oct 2025

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 321–340 of 398 recalls

Microvision Medical Holding B.V. Meibergdreef 45 Amsterdam Netherlands: MicroScan Lens Disposable Plastic Cap used with MicroScan...

Some lenses may have microscopic holes in the disposable caps representing a potential break in the sterile barrier

FDAJul 21, 2006CA, IN, IA +4 more• Microvision Medical Holding B.V. Meibergdreef 45 Amsterdam Netherlands

American Girl Children's Jewelry – Lead Poisoning (2006)

The recall includes American Girl necklaces, bracelets, earrings and hair accessories for girls. The recall does not include jewelry for American Girl dolls. The jewelry's packaging features a red and white cardboard backing with "American Girl" and "Made in China" written on the front.

CPSCMar 30, 2006Nationwide• American Girl Inc., of Middleton, Wis., a division of Mattel Inc., of El Segundo, Calif.

Bayer Healthcare, LLC (Diagnostics Division): ADVIA 2120 systems -Automated Complete Blood Cell and Dif...

The ADVIA 2120 has reported ; highly intermittent low results on all primary results: White Blood Cells (WBC), Red Blood Cells (RBC), Hemoglobin (HGB) and Platelets (PLT) and an abnormal baso cytogram.

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FDAMar 16, 2006Nationwide• Bayer Healthcare, LLC (Diagnostics Division)

Bayer Healthcare, LLC (Diagnostics Division): ADVIA 1650 Chemistry System, Automated Clinical Chemistry...

Low QC recovery observed on carbamazepine (CARB) results immediately following a Gentamicin (GENT) assay or a Digoxin (DIG) assay. When GENT or DIG precedes CARB, the CARB test result is artificially low (as much as -25%). PHNY was determined to also exhibit a similar carryover effect on CARB. All others were found not to produce the same reagent probe-based carryover effect.

FDAFeb 17, 2006PR• Bayer Healthcare, LLC (Diagnostics Division)

Bayer Healthcare, LLC (Diagnostics Division): Advia 2400 Chemistry System, Automated Clinical Chemistry...

FDAFeb 17, 2006PR• Bayer Healthcare, LLC (Diagnostics Division)

Bayer Healthcare, LLC (Diagnostics Division): ADVIA 1200 Chemistry System, Automated Clinical Chemistry...

FDAFeb 17, 2006PR• Bayer Healthcare, LLC (Diagnostics Division)

Bayer Healthcare, LLC (Diagnostics Division): Brand Name: RapidLab 1200 System, Model 1240, Part Number...

When stored data is recalled from memory, the results do not agree with the original results. Software anomaly: a calculation error occurs when using the correlation adjustment feature on the RapidLab 1200 Systems with software versions 1.0, 1.01, or 1.02. The correlation feature applies user-defined slope and offset parameters each time stored test results are recalled to the display.

FDAJan 20, 2006Nationwide• Bayer Healthcare, LLC (Diagnostics Division)

Medtronic Inc, Neurological & Spinal Division: Medtronic Activa Deep Brain Stimulation (DBS) system incl...

A safety concern exists regarding the Medtronic Activa Deep Brain Stimulation system instructions for performing MRI (magnetic resonance imaging). Medtronic's instructions have until now recommended a use of a displayed MRI head specific absorption rate (SAR) of not more than 0.4 W/kg. The recommended maximum displayed head SAR is now 0.1 W/kg.

FDANov 30, 2005Nationwide• Medtronic Inc, Neurological & Spinal Division

Medtronic Inc, Neurological & Spinal Division: Medtronic Model 37711 Restore Neurostimulator. The Resto...

A limited number of Model 37711 Restore Neurostimulators have an incorrect internal memory parameter that causes the device to indicate it is fully recharged when it may only be 80% to 90% recharged. This anomaly does not affect patient safety. This anomoly can be corrected by reprogramming the Restore Neurostimulator using specific software.

FDANov 22, 2005Nationwide• Medtronic Inc, Neurological & Spinal Division

C.R. Bard, Inc., Urological Division: Bard UroForce Balloon Dilation Catheter with Glissando Co...

There is a potential for the lumen to collapse and prevent passage over a guidewire.

FDANov 3, 2005Nationwide• C.R. Bard, Inc., Urological Division

C.R. Bard, Inc., Urological Division: Bard RespiShield * Closed Suction System with InnoValve *...

Varying degrees of difficulty were encountered when opening and closing the InnoValve.

FDASep 28, 2005Nationwide• C.R. Bard, Inc., Urological Division

C.R. Bard, Inc., Urological Division: Bard * Davol Reliavac 400 Closed Wound Suction Kit * Ster...

An incorrect Y-connector was placed in the kit.

FDAAug 17, 2005AL, CA, FL +6 more• C.R. Bard, Inc., Urological Division

Tiki Cone Metal Torch – Fire Safety Risk (2005)

Fire/Burn Risk

The recalled Tiki® Cone Metal Torch is a 6-foot-long outdoor open-flame lamp consisting of a black metal pole topped by a copper-colored, cone-shaped metal head. A black decorative rod spirals around the head of the torch. The torch head includes the fuel reservoir, cover and wick. It was sold under Lamplight Farms model numbers 1263 and 126301 and Wal-Mart item numbers 1656121 and 1691366. Both items were sold with the same UPC number 086861012635, which is located on the bottom of the printed hangtag.

CPSCJul 19, 2005Nationwide• Lamplight Farms Inc., a Division of W.C. Bradley Company, of Menomonee Falls, Wis.

Gas-Electric Heating Units (Trane/American Standard) – performance issue (2005)

Fire/Burn Risk

The recalled units include 2- through 5-ton Trane and American Standard heating and air conditioning packaged units. Affected units are combination gas heat and air conditioning systems installed outdoors only. Gas furnaces installed indoors are not included in this recall. The units have identification plates displaying the model number; serial number; and the year, month and day of manufacture. The plate is located on one end of the unit. The first four digits of all serial numbers indicate the year, fiscal week and day of manufacture. The recall includes: - All units with model numbers beginning with YCP or YCX and having serial numbers beginning with 3383 through 4475; - All units with model number beginning with YCY or YCZ and having serial numbers beginning with 4282 through 4475.

CPSCFeb 11, 2005Nationwide• Trane and American Standard, divisions of American Standard Inc., of Tyler, Texas

40-Watt Mini Spotlight Bulbs (Comtrad) – Fire Risk (2005)

Laceration Risk

The recalled 40-Watt "Type R" incandescent mini spot-light bulbs were included in two- and three-lamp accent lights in certain furniture hutch items manufactured by Sauder Woodworking Co. The furniture hutch models involved are: Model 9386 - Uses the three-lamp kit Model 9549 - Uses the two-lamp kit Model 9509 - Uses the two-lamp kit

CPSCJan 13, 2005Nationwide• Comtrad, Division of Waljon Ltd., Mississauga, Ontario, Canada

Medtronic Inc, Neurological & Spinal Division: Model 8561 Lioresal (Baclofen injection) Intrathecal Refi...

Outer package of Lioresal Intrethecal Refill Kit, model 8561, identifies the kit to contain 1-20 ml ampule of baclofen injection for intrathecal administration, 500 mcg/ml (10 mg/20 ml). Lot N0016487 incorrectly contains 1-20 ml ampule of baclofen concentration 2000 mcg/ml (40 mg/20 ml).

FDANov 19, 2004Nationwide• Medtronic Inc, Neurological & Spinal Division

Arc Fault Circuit Interrupters (Schneider) – Electrical Defect (2004)

Fire/Burn Risk

The recalled Square D QO® and Homeline® Arc Fault Interrupter circuit breakers are used with 15- and 20-amp branch circuits. They are required to be installed in bedroom circuits in accordance with the 2002 National Electrical Code. The recalled units were manufactured after March 1, 2004, and have a blue test button. The AFCI circuit breakers have one of the following date codes - CN, DN, EN, FN, GN, HN, or JN - stamped in red on the breaker label located just above the wiring terminal. The recalled units also have one of the following catalog numbers printed on a label on the front of the breaker: QO115AFI, QO115AFIC, QO120AFI, QO120AFIC, QOB115AFI, QOB120AFI, HOM115AFI, HOM115AFIC, HOM120AFI, HOM120AFIC, QO115VHAFI, QO120VHAFI, QOB115VHAFI, or QOB120VHAFI.

CPSCNov 3, 2004Nationwide• Schneider Electric North American Division, of Palatine, Ill.

Medtronic Inc, Neurological & Spinal Division: 8870 software application card versions AAA 02, BBB 04, B...

With the Model 8870 software application card versions AAA 02, BBB 04, BBC 02, and BBD 01, which is used in conjunction with the Model 8840 N'Vision Clinician Programmer, users may have mistakenly entered a periodic bolus interval into the minutes field, rather than the hours field, resulting in drug overdoses. This issue is limited to programming the SynchroMed and SynchroMed EL pumps.

FDAAug 24, 2004IN• Medtronic Inc, Neurological & Spinal Division

Ross Products Division Abbott Laboratories: Flexiflo Quantum Enteral Pump

Pumps were manufactured with an incorrect circuit board that may cause an increase in the feed rate and flush frequency of fluids.

FDAAug 18, 2004Nationwide• Ross Products Division Abbott Laboratories

Medtronic Inc, Neurological & Spinal Division: The Model 8540 Catheter Access Port Kit is intended for u...

The sterile tray label for the Model 8540 Catheter Access Port kit may be incorrectly labeled with a Model 8551 Refill kit label. The outer box of the affected Model 8540 Catheter Access Port kit is labeled correctly and the component parts within the sterile tray are the correct components for a Model 8540 Catheter Access Port kit. The issue is limited to one lot of product: CS0293.

FDAJul 23, 2004IN• Medtronic Inc, Neurological & Spinal Division