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. 2,582 recalls have been distributed to Delaware in the last 12 months.
Showing 14561–14580 of 27,373 recalls
Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...
The Issue: Potential for leaking product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...
The Issue: Potential for leaking product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...
The Issue: Potential for leaking product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExactaMix Recalled by The Metrix Company Due to Potential for leaking product
The Issue: Potential for leaking product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...
The Issue: Potential for leaking product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...
The Issue: Potential for leaking product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...
The Issue: Potential for leaking product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single-Use Biopsy Forceps Recalled by Micro-Tech (Nanjing) Co., Ltd. Due to...
The Issue: Single-Use Biopsy Forceps box contains incorrect product, instead it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue IABP Recalled by Maquet Datascope Corp - Cardiac Assist...
The Issue: There is a potential for interruption and/or inability to start therapy to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid IABP Recalled by Maquet Datascope Corp - Cardiac Assist...
The Issue: There is a potential for interruption and/or inability to start therapy to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AS-OBGYN Information System version 7.824.x Recalled by AS Software, Inc....
The Issue: Any change made to current ultrasound machine software or hardware upgrades,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost software 4.1.x and 4.2.x Recalled by Philips Medical...
The Issue: Stitching run on SkyPlate detector interrupted intermittently; Stitching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 (PB980) ventilator series: Puritan Bennett" 980...
The Issue: Software Update: External USB Drive performance and its impact on Graphic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Access Cortisol Reagent. REF (Catalog Number) 33600 Recalled by Beckman...
The Issue: Cross contamination may have occurred between wells for the reagent pack. As...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOND Slide Labeler Zebra Printer Model TLP3842 and Model GX4301 Recalled by...
The Issue: The power supply unit for the printer used with the device can potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Navigation 0-arm 02 Imaging System interventional fluoroscopic...
The Issue: O-arm 02 Imaging Systems correction to software version 4.1.0; new version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Agilis Steerable Introducer: indicated for introducing various...
The Issue: Reprocessed Agilis Steerable Introducers may not meet endotoxin requirements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NucliSENS¿ Magnetic Extraction Reagents Recalled by BioMerieux SA Due to...
The Issue: Data loggers showed that one shipment to the United States experienced low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH...
The Issue: A detector can detach and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as...
The Issue: Potential to lead to a false negative results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.