Reported Mar 11, 2015 · Terminated

The I-Cart is used to store, transport, and power video equipment used in medical procedures.

Richard Wolf Medical Instruments Corp.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Richard Wolf Medical Instruments Corp. · 353 Corporate Woods Pkwy · Vernon Hills, IL · 60061-3110

Is this the product you have?

  • The I-Cart is used to store, transport, and power video equipment used in medical procedures.
Lot codes and dates

3 of 3 products

Products covered by this recall
Model / numberProduct as published
31113.801The listed serial numbers are for the carts manufactured and include those that were distributed.) 1)
31113.701Serial Numbers: 1306000, 1306007, 1306014, 1306021, 1306103, 1306001, 1306008, 1306015, 1306022, 1306104, 1306002, 1306009, 1306016, 1306023, 1306105, 1306003, 1306010, 1306017, 1306024, 1307100, 1306004, 1306011, 1306018, 1306100, 1307101, 1306005, 1306012, 1306019, 1306101, 1307102, 1306006, 1306013, 1306020, 1306102, 1317103. 2)
Serial Numbers: 11001, 11011, 11020, 11030, 11039, 11048, 11058, 11002, 11012, 11021, 11031, 11040, 11049, 11059, 11003, 11013, 11023, 11032, 11041, 11050, 11060, 11005, 11014, 11024, 11033, 11042, 11051, 11061, 11006, 11015, 11025, 11034, 11043, 11052, 11063, 11007, 11016, 11026, 11035, 11044, 11053, 11064, 11008, 11017, 11027, 11036, 11045, 11055, 11065, 11009, 11018, 11028, 11037, 11046, 11056, 11066, 11010, 11019, 11029, 11038, 11047, 11057, 11067.
Amount recalled
83 carts

Where it was sold

  • Nationwide

Why it was recalled

The transformers installed on carts used for Richard Wolf medical video systems may overheat causing smoke and black plastic material to leak from the cart chassis.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jul 31, 2017 · Data as of Sep 19, 4:49 PM UTC

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