Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,474 recalls have been distributed to Delaware in the last 12 months.
Showing 22741–22760 of 27,373 recalls
Recalled Item: Xoran MiniCAT X-ray imaging device Recalled by Xoran Technologies, LLC Due...
The Issue: Out of tolerance kVp, Unexposed (black) frames, and Out of tolerance Dose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has become aware of a potential safety issue involving missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...
The Issue: The software issue described was corrected in the modification to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vantage Panoramic X-Ray System used to perform dental and orthodontic...
The Issue: Failure of the primary collimator may result in unintentional movement of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Recalled by Teleflex Medical Due to Misbranding: Although the product...
The Issue: Misbranding: Although the product labeling identifies the catheters as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aqauapak 728 SW Recalled by Teleflex Medical Due to Possibility that the...
The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak Adaptor Recalled by Teleflex Medical Due to Possibility that the...
The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...
The Issue: Aerogen has received a small number of complaints in relation to the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...
The Issue: Aerogen has received a small number of complaints in relation to the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Luminos Agile Max system The Luminos Agile is intended Recalled by...
The Issue: Two malfunctions posing potential risk to patients were identified with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Ysio Max system The Ysio Max is a radiographic system used in...
The Issue: Two malfunctions posing potential risk to patients were identified with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens AXIOM Luminos dRF Max systems The Axiom Luminos dRF Recalled by...
The Issue: Two malfunctions posing potential risk to patients were identified with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Uroskop Omnia Max system The Uroskop Omnia is a Recalled by Siemens...
The Issue: Two malfunctions posing potential risk to patients were identified with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...
The Issue: Aerogen has received a small number of complaints in relation to the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...
The Issue: Aerogen has received a small number of complaints in relation to the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure IQ Evolve Mattress Recalled by Arjo Hospital Equipment AB Due to...
The Issue: The firm received complaints regarding multiple mattresses were showing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dako Autostainer Link 48 with software version Dako Link 4.0.3 Recalled by...
The Issue: Dako is recalling the Dako Link 4.0.3 software on the Dako Autostainer Link...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Mass CKMB Isoenzyme Calibrator (MMB CAL) an in Recalled by...
The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista® Mass...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eFilm Workstation 4.0 and 4.0.1. eFilm Workstation is one of Recalled by...
The Issue: There is an issue related to eFilm Workstation versions 4.0 and 4.0.1 when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRx Vertical Positioner Recalled by Motion Concepts Due to Motion Concepts...
The Issue: Motion Concepts identified that there is a possibility of knee support...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.