Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
Tip holder portion of the scaler tip assembly may have an oversized condition that will not allow the scaler tip to stay seated in the holder may cause injury
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
GE HealthCare has become aware of the potential for loss of monitoring on CARESCAPE Canvas 1000, CARESCAPE Canvas Smart Display, and certain versions of CARESCAPE B850 and CARESCAPE B650…
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
41 mm acetabular outer heads were potentially assembled with a 42 mm locking ring, may lead to joint instability leading requiring surgical intervention
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
The reason for recall is the meters may show an incorrect measurement unit (mmol/L rather than mg/dL) and may result in the wrong unit of measure. Which may subsequently cause an error in…
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
Potential for coils to heat up and harm patients (burn).
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
The affected products may have been packaged with a defect in the sterile barrier seal. As a result, the integrity of the sterile barrier may be compromised.
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
Due to older version of Instruction for Use (IFU) instructing to ensure that the value and the sheath are tightly connected before use. This may cause users to over-tightening the luer…
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
Tip holder portion of the scaler tip assembly may have an oversized condition that will not allow the scaler tip to stay seated in the holder may cause injury
Device is not in full compliance to Type CF requirements of IEC 60601-1 and IEC 60601-2-34 standards. Therefore, there is a potential risk of electric shock. Health consequences may include…
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
Due to inadvertently disconnecting grounding cable of ultrasound system could result in electrical shock, electrical interference and/or equipment malfunction.
Browse recent months with enough recall history for useful comparison.
