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. 2,695 recalls have been distributed to Delaware in the last 12 months.
Showing 1241–1260 of 27,373 recalls
Recalled Item: STA-Liquid Anti-Xa 8. Model/Catalog Number: 00322US. The STA - Liquid...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA - Fibrinogen 5. Model/Catalog Number: 00674. The STA - Recalled by...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Ultra IABP Catheter Kit Product Name: Ultra IABP Recalled by...
The Issue: Device contains indications for use and device compatibility claims that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID...
The Issue: Their is a potential that the reamer may kick or bind up during or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: DJO SURGICAL Product Name: FA S Altivate Reverse Recalled by...
The Issue: Their is a potential that the reamer may kick or bind up during or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID...
The Issue: Their is a potential that the reamer may kick or bind up during or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID...
The Issue: Their is a potential that the reamer may kick or bind up during or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System Bardex I.C. Complete Care Infection Control...
The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System Lubri-Sil I.C. Complete Care Infection Control...
The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray Recalled by...
The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ReQuest Measles IgM Product Name: Enzyme Linked Immunoabsorbant...
The Issue: Measles IgM Test Kit lacks premarket approval or clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Pack Recalled by O&M HALYARD INC Due to Surgical drape packs may...
The Issue: Surgical drape packs may have open seals, which may compromise the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle 3 with TumorLOC Recalled by Philips Medical Systems (Cleveland) Inc...
The Issue: Due to software issue, Radiation Therapy Planning system may provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TOPS Inserter Recalled by PREMIA SPINE LTD Due to Potential for missing pins...
The Issue: Potential for missing pins at tip of inserter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chromophare Surgical Light System Recalled by Stryker Communications Due to...
The Issue: Surgical lights have stress lines forming on the powder coating, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prosthesis Head B Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Inconsistent size terminology and color coding used on labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic Trial Head Brown Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: Inconsistent size terminology and color coding used on labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Operating Tables Model Numbers: (1) 770001A0 Recalled by MAQUET GMBH...
The Issue: Under certain conditions, such as the simultaneous use of the operating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic...
The Issue: Specific lots of reprocessed electrophysiology catheters may contain small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Novum IQ Large Volume Pump Recalled by Baxter Healthcare Corporation...
The Issue: Baxter is issuing an Urgent Medical Device Correction for the Novum IQ large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.