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273 reported ongoing
306 records in this archive. Latest source date Aug 17, 2026.
FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Class IIReported ongoing
Distribution: Worldwide distribution.
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Class IIReported ongoing
Distribution: Worldwide distribution.
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Class IIReported ongoing
Distribution: Worldwide distribution.
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Class IIReported ongoing
Distribution: Worldwide distribution.
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Class IIReported ongoing
Distribution: Worldwide distribution.
The beds have a potential for an interface issue with the Rauland Responder 5 Nurse Call System where the bed exit system will alert at the bed, but may fail to send a remote alert through the nurse call system.
Class IIReported ongoing
Distribution: Worldwide distribution - US Nationwide. There was government and military distribution. The countries of Canada and Australia.
The Life2000 ventilator may fail to initiate the Low Gas Pressure alarm if the pressure gas source (Life2000 compressor, oxygen cylinder or wall source) is not supplied to the ventilator before initiating therapy.
Class IReported ongoing
Distribution: US nationwide distribution.
Baxter Healthcare Corporation has received increased customer reports of particulate matter in the Automated Compounding Device Inlets (disposable inlet), Product Codes H938173, H938174, H938175, H938176, used with the ExactaMix and ExactaMix Pro compounder...
Class IReported ongoing
Distribution: Worldwide distribution.
Baxter Healthcare Corporation has received increased customer reports of particulate matter in the Automated Compounding Device Inlets (disposable inlet), Product Codes H938173, H938174, H938175, H938176, used with the ExactaMix and ExactaMix Pro compounder...
Class IReported ongoing
Distribution: Worldwide distribution.
Baxter Healthcare Corporation has received increased customer reports of particulate matter in the Automated Compounding Device Inlets (disposable inlet), Product Codes H938173, H938174, H938175, H938176, used with the ExactaMix and ExactaMix Pro compounder...
Class IReported ongoing
Distribution: Worldwide distribution.
Baxter Healthcare Corporation has received increased customer reports of particulate matter in the Automated Compounding Device Inlets (disposable inlet), Product Codes H938173, H938174, H938175, H938176, used with the ExactaMix and ExactaMix Pro compounder...
Class IReported ongoing
Distribution: Worldwide distribution.
Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.
Class IReported ongoing
Distribution: Nationwide in the USA
The Spectrum WBM may fail to auto-document infusion status information back to the hospital's Electronic Medical Record (EMR) system. This software issue only impacts customers where the Spectrum V8 or Spectrum IQ infusion system is integrated with the hosp...
Class IIReported ongoing
Distribution: US, Nationwide
The Spectrum WBM may fail to auto-document infusion status information back to the hospital's Electronic Medical Record (EMR) system. This software issue only impacts customers where the Spectrum V8 or Spectrum IQ infusion system is integrated with the hosp...
Class IIReported ongoing
Distribution: US, Nationwide
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the PST 500 U Precision Surgical Table due to a potential issue with loose spring pins in the spindle drives. This can cause the tabletop to unexpectedly tilt or move at any ti...
Class IIReported ongoing
Distribution: Worldwide distribution - US Nationwide and the country of Canada.
Lack of Assurance of Sterility: Potential presence of leaks originating from the Connector Assembly component.
Class IIReported ongoing
Distribution: US Nationwide, Canada
Improperly performed testing prior to release
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of Florida.
The Braun Thermoscan PRO 6000 ear thermometers may have been shipped with a compact disc (CD) containing an outdated version of the Instructions for Use (IFU).
Class IIReported ongoing
Distribution: Distributed to United States, Canada, Australia, Malaysia, New Zealand, Philippines, Austria, Belgium, France, Germany, Italy, Netherlands, Norway, Spain, Sweden, and United Kin...
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products listed below. Specific VidiaPort and Trulight product codes are also impacted ...
Class IIReported ongoing
Distribution: Worldwide distribution.
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products listed below. Specific VidiaPort and Trulight product codes are also impacted ...
Class IIReported ongoing
Distribution: Worldwide distribution.
These examples come from this result page and are not a ranking of every recall reason.
This archive contains 306 records, including 273 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.
Compare the product, firm and lot, date, model or serial identifiers with the notice. Use the label-check guide if you need help locating an identifier.
A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.
This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. Check source coverage and the agency's current notices.
Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.