All Recalls

95,083 total recalls in our database

Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.

Apr 21, 2017 Surgical Instruments Nationwide View Details β†’

St. Jude Medical is providing all users of their HeartMate II LVAS with Pocket Controller with new software and updates to hardware to make the exchange to a backup controller easier. This is related to recall Z-1227/1230-2014.

Mar 30, 2017 Infusion Pumps View Details β†’

Mesa Laboratories is recalling Conductivity/TDS Calibrator Solution due to failure to meet product specifications.

May 12, 2017 Surgical Instruments Nationwide View Details β†’
πŸ₯ Medical Devices Class I - Dangerous

There is a possibility of a data acquisition disruption that may cause an unusual light scatter event pattern for the white blood cell differential that may not have a system flag and/or message. The events associated with the unusual light scatter pattern may be incorrectly removed from analysis which can result in an erroneous differential result.

Apr 24, 2017 Other Medical Devices Nationwide View Details β†’

Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.

Apr 21, 2017 Surgical Instruments Nationwide View Details β†’

St. Jude Medical is providing all users of their HeartMate II LVAS with Pocket Controller with new software and updates to hardware to make the exchange to a backup controller easier. This is related to recall Z-1227/1230-2014.

Mar 30, 2017 Other Medical Devices View Details β†’

Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.

Apr 21, 2017 Surgical Instruments Nationwide View Details β†’

Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.

Apr 21, 2017 Surgical Instruments Nationwide View Details β†’

Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.

Apr 21, 2017 Surgical Instruments Nationwide View Details β†’

There is a possibility of a data acquisition disruption that may cause an unusual light scatter event pattern for the white blood cell differential that may not have a system flag and/or message. The events associated with the unusual light scatter pattern may be incorrectly removed from analysis which can result in an erroneous differential result.

Apr 24, 2017 Other Medical Devices Nationwide View Details β†’

Zimmer Biomet is conducting a medical device field action for the SpF PLUS-Mini and SpF XL IIB Implantable Spinal Fusion Stimulator products due to higher than allowed cytotoxicity levels found during routine process monitoring with the product.

Apr 20, 2017 Implants & Prosthetics Nationwide View Details β†’

Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.

Apr 21, 2017 Surgical Instruments Nationwide View Details β†’

Cordless electric lawn mowers

Hongkong Sun Rise Trading Ltd., of China

🏠 Consumer Products Class I - Dangerous

The circuit board in the lawn mower can short circuit and catch fire, posing a fire hazard to users.

May 26, 2017 Electronics Nationwide View Details β†’

Digital clamp meters

Unknown Manufacturer

🏠 Consumer Products Class I - Dangerous

The meters can fail to give an accurate voltage reading, resulting in the operator falsely believing the electrical power is low or off, posing an electrocution hazard.

May 25, 2017 Clothing & Accessories Nationwide View Details β†’