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. 1,741 recalls have been distributed to Delaware in the last 12 months.
Showing 41061–41080 of 48,330 recalls
Recalled Item: Sterile Water for Injection Recalled by Flawless Beauty LLC Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vitamin C (ascorbic acid) Injection Recalled by Flawless Beauty LLC Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Parenteral product is sold over the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Red Yeast Rice High Potency Dietary Supplement Recalled by Independent...
The Issue: Marketed Without An Approved NDA/ANDA: Product is being recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Laroscorbine Platinium (vitamin C/collagen) injectable I.V. solution...
The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Saluta (reduced glutathione) Powder for Injection Recalled by Flawless...
The Issue: Marketed Without An Approved NDA/ANDA: Parenteral product is labeled for use...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Relumins Advanced Glutathione (lyophilized glutathione/vitamin C) injectable...
The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Coaxial Micro-Introducer Kit. Greatbatch Part Number/Bard Access Systems...
The Issue: Greatbatch identified that the documentation does not support the five-year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...
The Issue: Connection issues between the PD transfer set catheter connector and an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PediaCare brand DAY & NIGHT Value Pack DAYTIME MULTI-SYMPTOM Cold Recalled...
The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PediaCare brand NIGHTTIME MULTI-SYMPTOM Cold Recalled by Prestige Brands...
The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Revision K Actuator Test Boards sold as replacement parts for Recalled by...
The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BG3515-5 US 5mL BioGlue Surgical Adhesive. BioGlue Surgical Adhesive...
The Issue: Serum albumin component monomer failed to meet internally established end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation software version 4.0.3.4 RayStation is a software system designed...
The Issue: This notice concerns a problem with the computation of ROI voxel volumes for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oasis Coil Extension Cable used with Hitachi Oasis MRI System Recalled by...
The Issue: The firm received a complaint stating the Coil Extension Cable accessory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008T Hemodialysis Machine with Revision K Actuator Test Boards...
The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PATIENT TRACKER 9733534XOM ENT 1PK Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UPGRD PRGM 9734638 ADD AxiEM NAVIGATION Recalled by Medtronic Navigation,...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRAPE 9732722 TUBE STERILE O-ARM 20PK Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUMOR RES. PACK 9733553 AxiEM S.M. Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT Recalled by Medtronic Navigation, Inc. Due to Medtronic Navigation is...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.