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Smiths Medical MD, Inc.

Smiths Medical MD, Inc. Recalls

All product recalls associated with Smiths Medical MD, 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 32321–32340 of 37665 recalls

Smiths Medical MD, Inc.: Smiths Medical Medfusion Model 3500 Syringe Infusion Pump...

Delay in therapy. Keypad issues with Medfusion Syringe Infusion Pump, model numbers 3500-306 and 3500-415 ("Pump") have occurred during implementation or shortly after first being placed into use. These issues can be intermittent, and may render the Pump inoperable or the Pump may not respond to certain keypad button presses.

FDADec 18, 2008Nationwide• Smiths Medical MD, Inc.

Zevex International, Inc.: EnteraLite Infinity Enteral Feeding Pump, REF INFP01, Zev...

Enteral feeding pumps may not accurately deliver fluid, potentially under-infusing or over-infusing.

FDADec 18, 2008Nationwide• Zevex International, Inc.

Alphatec Spine, Inc.: ROC Lumbar bolt caddy, Part Number: 81997-01-05. Sterili...

Alphatec discovered that the lot of bolt caddies had the incorrect bolt length laser etched on one side of the caddy. The actual ROC bolts themselves are correctly laser etched.

1...1615 161616171618 1619...1884

Page 1617 of 1884Next

FDADec 16, 2008Nationwide• Alphatec Spine, Inc.

Mountain Cat Snowmobiles (Arctic Cat) – Fire Hazard (2008)

Fire/Burn Risk

This recall involves all 2009 model Mountain Cat and Crossfire snowmobiles within the Vin number range of 103896 through 118441. The Vin number can be found stamped into the tunnel near the right-side footrest.

CPSCDec 16, 2008Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.

Newport Medical Instruments Inc: Newport e360 Ventilator, Rx only. The e360 Ventilator S...

In December 2008, Newport initiated a field correction to upgrade e360 ventilators with software versions 3.0 or higher to software version 3.3. As a result of this upgrade, some customers experienced unexpected device alert alarms. Newport's investigation into these complaints confirmed that the 3.3 software responds too quickly to certain situations, giving a false device alert. Newport condu

FDADec 15, 2008AL, AZ, CA +20 more• Newport Medical Instruments Inc

GE Healthcare Integrated IT Solutions: Centricity Enterprise Web 3.0 software; the software allo...

Software error: There are two potential safety situations with Centricity Enterprise Web software - a forced log off may occur while using the Centricity Enterprise Web during an open session, and Centricity Enterprise Web does not utilize calibration performed on image measurements in Centricity RA1000 Workstation.

FDADec 12, 2008Nationwide• GE Healthcare Integrated IT Solutions

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

There is a potential patient safety issue involving the use of the F12 keyboard Approve & Complete function. The issue may cause erroneous information to be added to a report when trying to approve and complete it.

FDADec 12, 2008Nationwide• GE Healthcare Integrated IT Solutions

Commercial Frozen Food Merchandisers (Tyler) – Fire Hazard (2008)

Fire/Burn Risk

The recalled Vertical Multi-deck Frozen Food Merchandisers are typically used in grocery stores and other commercial settings. The recall involves models D6F, D6FL, L6F, L6FL, N6F and N6FL manufactured between 1995 and 2008. The serial and model numbers are located on the label located on the inside, upper-right front of the unit behind the lighting assembly. A complete list of the serial numbers involved in this recall can be found at www.tylerrefrigeration.com

CPSCDec 11, 2008Nationwide• Tyler Refrigeration, of Niles, Mich.

Power Sweep Electric Blowers (Toro) – Projectile Hazard (2008)

The recall involves Toro Power Sweep electric blower model 51586 that was manufactured between 2000 and 2002. The recalled units have serial numbers that range between 000055100 and 220255609. There are two decals on the main housing of the blower. One decal reads, "TORO Power Sweep" and the decal on the opposite side of the blower contains the model number and serial number (shown by the letter "A" in the picture). The recalled units can be identified by a black impeller fan, which can be seen through the air inlet screen on the bottom of the unit.

CPSCDec 11, 2008Nationwide• The Toro Company, of Bloomington, Minn.

Napoleon Gas Fireplace Inserts (Wolf Steel) – Laceration Risk (2008)

Fire/Burn Risk

This recall involves Napoleon propane GDI44 gas fireplace inserts. Model number GDI44 is located on the front cover of the operating instructions or on the rating label found behind the right side panel next to the insert's viewing glass. The glass size is 36" wide and 22" high. Napoleon natural gas GDI44 inserts are not affected by this recall.

CPSCDec 11, 2008Nationwide• Wolf Steel USA, of Crittenden, Ky.