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 15061–15080 of 27,373 recalls
Recalled Item: Duo-Flow XTP Straight Full Set Recalled by Medical Components, Inc dba...
The Issue: The suture wings have the potential to crack or break. Potential patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides failed to meet current claims for Limit of Blank (LoB), Limit of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arkon Anesthesia Delivery System with Arkon Software Version 2.70 Recalled...
The Issue: Arkon Anesthesia Delivery System may go into a failed state (mechanical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CREA Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides did not meet the current claims for Limit of Blank (LoB), Limit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...
The Issue: The packaging may not be sealed. If the packaging is compromised in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...
The Issue: The packaging may not be sealed. If the packaging is compromised in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChloraPrep With Tint Recalled by Merit Medical Systems, Inc. Due to A...
The Issue: A nonsterile bulk product designated for further processing in a tray was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroLift System Number: UL400-4 Tray Contents: UroLift System Recalled by...
The Issue: Upon implant deployment, the Capsular Tab may not be delivered as the needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbViser AutoValve IAP (intra- abdominal pressure) Monitoring Device Recalled...
The Issue: Bubble Leak Testing on AbViser AutoValve IAP Monitoring Devices without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 analyzer Recalled by Radiometer America Inc Due to The analyzer...
The Issue: The analyzer software may cause a mis-match of patient demographics and test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended Recalled...
The Issue: Incorrect expiration being entered for one lot.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Powder Free Vinyl Exam Gloves Recalled by Cypress Medical Products LLC Due...
The Issue: The firm is recalling one lot of McKesson Powder Free Vinyl Exam Gloves...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTOVi Tracker/Scanner Recalled by Hudson Scientific LLC Due to The device...
The Issue: The device and its accessories may not have been manufactured according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.