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. 2,559 recalls have been distributed to Delaware in the last 12 months.
Showing 17781–17800 of 27,373 recalls
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8.5MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shandon Rapid Chrome Kwik-Diff Kit Part Number: 9990700 Shandon Rapid...
The Issue: Methylene Blue, Solution #3 in the Kwik Diff Kit was not Methylene Blue but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pausch Uroview FD fluoroscopic X-ray system UDI number (01)04260491620040...
The Issue: During patient interventions with the urology table the radiation is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Connect Diabetes Management App versions 2.0.0 Recalled by Roche...
The Issue: A program error (bug) in the Bolus Advisor feature, which could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bedside monitor CSM-1901(Life Scope G9) with main unit CU-192RA. The...
The Issue: The Pause function on central monitors will not automatically resume when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerate Pheno system Recalled by Accelerate Diagnostics Inc Due to Rare...
The Issue: Rare isolates of Enterobacteriaceae may generate a susceptible meropenem...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Measurement Specialties Reusable Temperature Probe Autoclavable. Sold as...
The Issue: The reusable temperature probes are provided with instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Small Particle Aerosol Generator Model SPAG-2 6000 Series (SPAG-2). The...
The Issue: SPAG-2 unit nebulizers from Lot J0571670RA were tested at Next Breath for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is...
The Issue: Product shipped proximate to or past the expiration date listed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product...
The Issue: In April 2015, HeartWare, now a part of Medtronic, notified users of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW Recalled by Smith &...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm CE Recalled by Cincinnati Sub-Zero Products Inc Due to Improperly...
The Issue: Improperly rated fuses were used in the manufacture of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 02419937 Recalled by Siemens...
The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 03896216 Recalled by Siemens...
The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 09010686 Recalled by Siemens...
The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen (TM) Laboratory Automation Systems using all TCAutomation(TM) Software...
The Issue: Software anomaly; Thermo-Fisher Scientific initially discovered and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: uNion Cervical Plate System Product Usage: The uNion Cervical Plate Recalled...
The Issue: Surgical technique was revised to prevent static plate screws blocking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.