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 15701–15720 of 27,373 recalls
Recalled Item: Accelerate PhenoTest BC kit Recalled by Accelerate Diagnostics Inc Due to...
The Issue: The kits may produce an elevated rate of false positive calls for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart (HS1) Onsite/Home AED Recalled by Philips Electronics...
The Issue: An issue with one of the electric components (a resistor) could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray BCID Panel (Blood Culture Identification Panel) Recalled by...
The Issue: There is an increased risk of false positive Proteus results when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Surgical Cassette Tapered Implants are intended for placement...
The Issue: The surgical cassette contained extra-large white grommets making the 3.8 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Prestige LP(TM) Cervical Disc System with Streamlined Instruments...
The Issue: The firm received complaints of drill bits breaking during use with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Nail System Recalled by Zimmer Biomet, Inc. Due to Certain lots of...
The Issue: Certain lots of the Phoenix Tibia Nail 3.5mm Inserter instruments are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length...
The Issue: Products have been packaged with the wrong Trocar length type.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...
The Issue: The power load floor plates which hold the ambulance cot anchors in place...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vacuum Regulator Recalled by Ohio Medical Corporation Due to Final quality...
The Issue: Final quality control testing was not completed before the devices were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation...
The Issue: The wrong parts were picked for packaging. The connecting Nuts were packed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X Surgical System Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Specific da Vinci X Surgical Systems (IS4200) were shipped with defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK Estradiol Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK IGE II Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK BMG Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK C-Peptide II Recalled by Tosoh Bioscience Inc Due to Asfotase...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK HCG Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK Myoglobin Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK SHBG Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK TSH 3rd Generation Recalled by Tosoh Bioscience Inc Due to Asfotase...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK IRI Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.