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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

896

Class I (Serious)

125

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 15661–15680 of 17592 recalls

Smiths Medical MD, Inc.: Smiths CADD Medication Cassette Reservoirs with Clamp and...

Leakage associated with the CADD Medication Cassette Reservoirs for use with the CADD Ambulatory Infusion Pumps

FDADec 14, 2007AL, AK, AZ +48 more• Smiths Medical MD, Inc.

Smiths Medical MD, Inc.: Smiths CADD Yellow Medication Cassette Reservoirs with Cl...

Leakage associated with the CADD Medication Cassette Reservoirs for use with the CADD Ambulatory Infusion Pumps

FDADec 14, 2007AL, AK, AZ +48 more• Smiths Medical MD, Inc.

OEC Medical Systems, Inc: GE Healthcare OEC 9900 mobile fluoroscopic x-ray system

Possible overexposure: Failure to apply the entrance exposure rate (EER) tube current limit calibration to the automatic exposure rate (AER) control system when the anatomical profile mode is changed from the default selection to another selection. Manual technique modes are not affected.

FDA

1...782 783784785 786...880

Page 784 of 880Next

Dec 14, 2007

Nationwide

• OEC Medical Systems, Inc

VISX INCORPORATED, A SUBSIDIARY OF AMO INC: AMO VISX STAR Excimer Laser System, manufactured by VISX,...

Firm received two complaints (including one injury complaint) associated with the movement of the VISX chair while in the patient loading ("fully swung out" unlocked) position under an IntraLase FS laser.

FDADec 13, 2007AL, AK, AZ +47 more• VISX INCORPORATED, A SUBSIDIARY OF AMO INC

Booster Cables (AutoZone) – Electrical Hazard (2007)

This recall involves the Valucraft eight gauge and ten gauge booster cables. The cables are orange and have "8GA" or "10GA" printed on them.

CPSCDec 13, 2007Nationwide• AutoZone Parts Inc., of Memphis, Tenn.

Philips Medical Systems North America Co. Phillips: DigitalDiagnost X-ray System is a stationary Diagnostic X...

When using DICOM print functionality, the printed images may contain data for the wrong patient.

FDADec 13, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Billy Goat MultiVac Outdoor Vacuums (Billy Goat) – fire hazard (2007)

Fire/Burn Risk

The recalled outdoor vacuum is black and green with a red motor housing. "Billy Goat" is printed on the vacuum's bag. Only outdoor vacuums with the following model and serial numbers are included in the recall. The model and serial numbers are printed on a label located directly below the height adjustment crank on the left side of the vacuum. Models MV650H MV650SPH Serial Numbers 061107xxx 061807xxx 062507xxx 070907xxx 072407xxx 073007xxx 080607xxx 081307xxx 082007xxx 082707xxx 090407xxx 091007xxx

CPSCDec 12, 2007Nationwide• Billy Goat Industries Inc, of Lee's Summit, Mo.

Polaris Ranger RZR 800 EFI (Polaris) – fire hazard (2007)

Fire/Burn Risk

Model Year 2008 Polaris Ranger RZR 800 EFI utility vehicles with model number R08VH76AD (red), and model number R08VH76AG (green) are included in this recall. They were manufactured between August 21, 2007 and October 3, 2007. The model number decal is located under the passenger seat.

CPSCDec 6, 2007Nationwide• Polaris Industries Inc., of Medina, Minn.

Wall Microwave Ovens (GE) – Fire Risk (2007)

Fire/Burn Risk

The recall includes GE combination microwave and conventional built-in wall ovens sold under the following brand names: GE, GE Profile® and Kenmore. The ovens were sold in white, black, bisque and stainless steel. The brand name is printed on the lower left corner on the front of the microwave door. The following model and serial numbers can be found inside the microwave oven on the left interior wall. Recalled Models Serial number begins with: GE / GE Profile JKP85B0A3BB, JKP85B0D1BB, JKP85W0A3WW, JKP85W0D1WW, JKP86B0F1BB, JKP86C0F1CC, JKP86S0F1SS, JKP86W0F1WW, JT965B0F1BB, JT965C0F1CC, JT965S0F1SS, JT965W0F1WW, JTP85B0A2BB, JTP85B0A3BB, JTP85B0A4BB, JTP85B0A5BB, JTP85B0D1BB, JTP85W0A2WW, JTP85W0A3WW, JTP85W0A4WW, JTP85W0A5WW, JTP85W0D1WW, JTP86B0F1BB, JTP86C0F1CC, JTP86S0F1SS, JTP86W0F1WW, JTP95B0A2BB, JTP95B0A3BB, JTP95B0A4BB, JTP95B0A5BB, JTP95B0D1BB, JTP95W0A2WW, JTP95W0A3WW, JTP95W0A4WW, JTP95W0A5WW, JTP95W0D1WW AZ, DZ, FZ, GZ, HZ, LZ, MZ, RZ, SZ, TZ, VZ, ZZ, AA, DA, FA, GA, HA, LA, MA, RA, SA, TA, VA, ZA, AD, DD, FD, GD, HD, LD, MD, RD, SD, TD, VD, ZD, AF, DF, FF, GF, HF, LF, MF, RF, SF, TF, VF, ZF Kenmore (All model numbers start with 911) 41485991, 41485992, 41485993, 41485994, 41489991, 41489992, 41489993, 41489994, 49485992, 49489992, 47692100, 47699100, 47862100, 47869100, 47812200, 47813200, 47814200, 47819200, 47792200, 47793200, 47794200, 47799200 0, 1, 2, 3

CPSCDec 5, 2007Nationwide• GE Consumer & Industrial, of Louisville, Ky.

Rockwell Medical Technologies, Inc: RenalPure Liquid Acid Concentrate R-006; One Gallon (3.78...

Foil Seal Deterioration; occuring on the tamper resistant foil seals on dialysis liquid concentrate and Dri-Sate product containers older than two years old.

FDADec 3, 2007Nationwide• Rockwell Medical Technologies, Inc

Medtronic Neuromodulation: Medtronic Bravo pH Capsule with Delivery System, Stomach ...

Unable to detach from source: The capsule may not detach from the delivery system following attachment to the esophageal wall.

FDADec 3, 2007AL, AK, AZ +48 more• Medtronic Neuromodulation

Rockwell Medical Technologies, Inc: Glacial Acidic Acid (liquid component of Dri-Sate Dry Ac...

Foil Seal Deterioration; occuring on the tamper resistant foil seals on dialysis liquid concentrate and Dri-Sate product containers older than two years old.

FDADec 3, 2007Nationwide• Rockwell Medical Technologies, Inc

Fresenius Medical Care North America: Optiflux 180NR Advanced Fresenius Polysulfone, Catalog No...

Leaking: the Dialyzer may leak at the header resulting in small amounts of blood loss.

FDADec 3, 2007Nationwide• Fresenius Medical Care North America

Rockwell Medical Technologies, Inc: Dri-Sate Glacial Acidic Acid (liquid component of Dri-Sat...

Foil Seal Deterioration; occuring on the tamper resistant foil seals on dialysis liquid concentrate and Dri-Sate product containers older than two years old.

FDADec 3, 2007Nationwide• Rockwell Medical Technologies, Inc

Computerized Medical Systems Inc: Focal Radiation Treatment Planning System, Focal Release...

Focal: when a plan is sent to Focal from XiO and the structure properties are edited in Focal CT Sim activity, these changes result in changes to the MLC or field size for the plan when they should not. XiO will recalculate dose when modified plan is returned to XiO however the user may not notice that it has changed form the plant they had approved earlier. Editing the structure properties (col

FDANov 30, 2007Nationwide• Computerized Medical Systems Inc

Philips Medical Systems North America Co. Phillips: MultiDiagnost Eleva Flat Detector X-Ray System; Part Numb...

Delay in Imaging: MultiDiagnost Eleva with Flat Detector x-ray system cannot perform fluoroscopy procedures while certain image file housekeeping operations are performed. Fluoroscopy cannot be performed and new exposures are not able to be acquired until the housekeeping operations are complete which may take several minutes. The loss of system availability could occur during an interventional

FDANov 29, 2007CO, MN, NJ +2 more• Philips Medical Systems North America Co. Phillips

Sliding Miter Saws (Performax) – Laceration Risk (2007)

Laceration Risk

The recall includes Performax model number 90206 and Wilton model number 34570 10-inch sliding miter saws with date code/serial numbers ranging from W062505 to W070405. The model, date code/serial numbers are printed on a black label on the motor housing of the saw.

CPSCNov 27, 2007Nationwide• WMH Tool Group Inc. (WMH), of Elgin, Ill.

Allen Medical Systems, Inc. One Post Office Square: Allen Medical C-Flex, Polar Head Positioner Catalog Numbe...

Handle jamming in the open position, preventing the device from adequately supporting the head during spinal surgery. Possible delay in surgery, or injury.

FDANov 27, 2007MA, MS• Allen Medical Systems, Inc. One Post Office Square

Smith And Nephew, Inc. Wound Management Division: Smith & Nephew, Inc., Exu-Dry Wound Burn Dressing, Produc...

Sterility (package integrity) compromised: Distribution of product that did not meet specifications; open seals.

FDANov 21, 2007Nationwide• Smith And Nephew, Inc. Wound Management Division

Philips Medical Systems (Cleveland) Inc: Rotate Motion Shunt Resistor Kit, Scintillation (gamma) c...

Fire/Burn Risk

Resistor Failure: The Rotate Motion Shunt Resistor may overheat and results in the appearance of smoke, a burning smell, and an electronic stop condition, which will disable the gamma camera rotate motion and all other motions.

FDANov 21, 2007AL, AZ, CA +42 more• Philips Medical Systems (Cleveland) Inc