Recall: Puritan Bennett 980 (PB980) Ventilator Series
On 2018-12-18, the FDA announced that Medtronic is conducting a recall on 980 (PB980) Ventilator Series due to a possible software update. The recalled products were sold under the brand name(s) Puritan Bennett during an unspecified time period throughout the regions shown in the map below.
In recent months, there have been 1 medical devices recalls due to potential software update. Additionally, there have been 3 drug and medical device recalls due to other health hazards as well as 97 food recalls.
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Detailed Recall Information
Regions Where Sold: Because the region was not specified, it is assumed that this product was available nationwide.
Product Description: 980 (PB980) Ventilator Series
Brand Name(s): Puritan Bennett
Reason for Recall: Software update
Official Recall Date: 2018-12-18
Additional information provided by the FDA.gov:
Medtronic (NYSE:MDT) is notifying customers worldwide of a voluntary field corrective action for its Puritan Bennett 980 (PB980) ventilator series. Medtronic initiated this field action on September 19, 2018. Read More.
More information may be available at FDA.gov
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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.