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. 2,623 recalls have been distributed to Delaware in the last 12 months.
Showing 12181–12200 of 27,373 recalls
Recalled Item: SIEMENS Healthineers Luminos Agile Max Model: 10762472 - Product Usage:...
The Issue: Two software issues (1) Using the override function in case of blocked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...
The Issue: Potential for thermal damage near the power cord connector and Power Entry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spy-Phi Drape only (HH2020) Pack of 20 HH2000 (Sold internationally Recalled...
The Issue: Sterile drapes packaged in an unsealed pouch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spy-Phi Drape (HH2000) sold as a Spy-Phi Pack (HH9006). Only Recalled by...
The Issue: Sterile drapes packaged in an unsealed pouch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex ProVent Arterial Blood Sampling Kit with Dry Lithium Heparin Recalled...
The Issue: Lots of Smiths Medical Portex Pro-Vent and LineDraw Arterial Blood Sampling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...
The Issue: Potential for thermal damage near the power cord connector and Power Entry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex LineDraw Arterial Blood Sampling Syringe with Dry Lithium Heparin...
The Issue: Portex Pro-Vent and LineDraw Arterial Blood Sampling syringes may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Humidity Pack (Qty 1) Recalled by Siemens Healthcare...
The Issue: A software error is causing the analyzer to incorrectly eject affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Brain 3.0 Application-Brain Recalled by MEDTECH SAS Due to Some...
The Issue: Some cross-sectional images from the image acquisitions of the patients head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Humidity Pack (Qty 5) Recalled by Siemens Healthcare...
The Issue: A software error is causing the analyzer to incorrectly eject affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA One 3.1 Brain Application Recalled by MEDTECH SAS Due to Some...
The Issue: Some cross-sectional images from the image acquisitions of the patients head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coated VICRYL (Polyglactin 910) Suture Recalled by Ethicon, Inc. Due to Some...
The Issue: Some sutures in the lot may exhibit a small section of braid fraying, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC...
The Issue: When inflating/deflating a single bladder, both bladders could potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medonic M-Series Hematology Analyzer M16S BD ABR US Product code: 1400075...
The Issue: A mix-up of autosampler tube positions with a possibility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TwinFix Ti 2.8 mm HS Suture Anchor - Product Usage: Recalled by Smith &...
The Issue: Due to a potential for sterile barrier breach. A complaint was received that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Exper FD Series. System codes 722003 722010 722022 722005 Recalled by...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.