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 22941–22960 of 27,373 recalls
Recalled Item: Verigene BC-GN Test Kit (Catalog number 20-005-021) includes: 1) 20 Recalled...
The Issue: Nanosphere Inc. has recently determined through four customer complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kodak DirectView DR 7500 Diagnostic X-Ray System Product Usage: The Recalled...
The Issue: An on-site evaluation of the equipment parts that attach the Beta Assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gyrus ACMI Falope-Ring Dilator Recalled by Gyrus Medical, Inc Due to...
The Issue: Falope-Ring Dilator for Reusable Falope-Ring Band Applicators have been sold...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System --- For use in the in vitro quantitative...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Possible sound loss...
The Issue: Possible sound loss associated with the CARESCAPE Monitor B650. When an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Luminos dRF Recalled by Siemens Medical Solutions USA, Inc Due to It...
The Issue: It was discovered that during a RAD examination using Siemens Luminos dRF,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System --- For use in the in vitro quantitative...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excella II Standard Pedicle Screw Recalled by Innovasis, Inc Due to Mislabeling
The Issue: Innovasis is recalling the Excella II Standard Pedicle Screw due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Recalled by Codman &...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelePACS software versions 3-8-1 to 4-9-1 Recalled by Intelerad Medical...
The Issue: In specific situation a partially truncated file may be written to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Device Recalled by Codman &...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In line Valve with Unitized BACTISEAL¿ Catheter and...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with Catheter and Accessories Recalled by...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Device Recalled by Codman &...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with Unitized Catheter and Accessories...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve only with SIPHONGUARD¿ Device Recalled by...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve Only Recalled by Codman & Shurtleff, Inc. Due...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIGEN(R) INTERTAN(TM) 10MM X 18 CM NAIL Recalled by Smith & Nephew, Inc....
The Issue: There was an error in manufacturing which resulted in the proximal lag screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EN MENTOR Round High Profile Single Use Saline Breast Implant Recalled by...
The Issue: The device labeling is stamped with 330cc and the device is actually 380cc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.