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. 2,457 recalls have been distributed to Delaware in the last 12 months.
Showing 27161–27180 of 27,373 recalls
Recalled Item: Z-800 Volumetric Infusion System. For intravenous infusion of parenteral...
The Issue: Update Instruction For Use for Preventative Maintenance (PM) Schedule and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian High Energy Clinacs Recalled by Varian Medical Systems, Inc. Oncology...
The Issue: Under certain conditions, photon beams in High Energy Clinacs may experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioDerm Liberty Pouch Clean & Dry External Male Catheter Specialty Recalled...
The Issue: On 06/08/2011, BioDerm, Inc. issued a voluntary recall of a component skin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioDerm Safe n' Dry 21006 (Component: SKIN-PREP Protective wipes). The...
The Issue: On 06/08/2011, BioDerm, Inc. issued a voluntary recall of a component (Smith...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioDerm Liberty 3.0 External Male Catheter Specialty Type with integral...
The Issue: On 06/08/2011, BioDerm, Inc. issued a voluntary recall of a component skin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune¿ 2 Rover - ULTRA ~120V ~ 60 Hz 12A Recalled by Stryker Instruments...
The Issue: Beginning May 24, 2011 Stryker Neptune 2 (N2) Waste Management Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune¿ 2 Rover - ULTRA ~230V ~ 50 Hz 12A Recalled by Stryker Instruments...
The Issue: Beginning May 24, 2011 Stryker Neptune 2 (N2) Waste Management Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******Qty 1*** EC REP*** ConMed Linvatec Xenon Universal Light Source...
The Issue: Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source Recalled by...
The Issue: Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DPM Central Station Mindray DS USA Recalled by Mindray DS USA, Inc. d.b.a....
The Issue: There is a software anomaly with the DPM Central Monitoring System where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Catalog (part number 20-0020) utilized with the Electric and...
The Issue: Anspach Effort, Inc. Palm Beach Gardens, FL initiated a correction of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pneumatic Systems Operating Manual (part numbers 19-0005) utilized with the...
The Issue: Anspach Effort, Inc. Palm Beach Gardens, FL initiated a correction of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cutting Bur Chart (part number 20-0019) utilized with the Electric Recalled...
The Issue: Anspach Effort, Inc. Palm Beach Gardens, FL initiated a correction of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lithium Thionyl non-rechargeable disposable battery pack P/N 350-0294-00...
The Issue: Braemar Inc., became aware of a battery related incident that occurred with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunquest Laboratory SMART & Sunquest Laboratory SMART Select Recalled by...
The Issue: In Online Entry (OEx) there are two scenarios where a Test result from one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IO Fix IntraOsseous Fixation System Recalled by Extremity Medical LLC Due to...
The Issue: Product Event Reports revealed that lag screw passes through washer (e.g....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE LightSpeed CT750 HD The GE LightSpeed CT750 HD Computed Recalled by GE...
The Issue: GE Healthcare conducted a recall involving 2 events affecting the GE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780303601 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780303602...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00789502801 VerSys Femoral Head Provisional 28mm -3.5 00789502802 VerSys...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780304001 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780304002...
The Issue: Complaints have been received reporting sub-optimal fit between provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.