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. 960 recalls have been distributed to Delaware in the last 12 months.
Showing 34441–34460 of 48,330 recalls
Recalled Item: ZI XIU TANG BEAUTY FACE & FIGURE Capsules Recalled by Bee Extremely Amazed...
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lindane Lotion Recalled by Morton Grove Pharmaceuticals, Inc. Due to...
The Issue: Super-Potent Drug: Out of Specification Assay test results were reported for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oasis Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Anesthesia device service kits. ASSY-MSN Recalled by GE Medical Systems, LLC...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-10 Rack Loader Recalled by Bio-Rad Laboratories, Inc. Due to On a rare...
The Issue: On a rare occasion, there is a potential to assign a patient result to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and...
The Issue: The door latch may not fully close and the door may open unexpectedly. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A Recalled...
The Issue: An issue with the Panorama Central Station may cause the system to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FMC7 FITC Recalled by Becton, Dickinson and Company, BD Biosciences Due to...
The Issue: Becton, Dickinson and Company (BD) has determined that the FMC7 FITC (ASR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI¿ H/S Cuvette The intended use for the CDI¿ H Recalled by Terumo...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received complaints of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FUEL UP PLUS Recalled by Reesna, Inc Due to Undeclared Hydroxythiohomosildenafil
The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FUEL UP HIGH OCTANE Recalled by Reesna, Inc Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IBA Dosimetry GmbH Lift Table Type 4320 Recalled by Iba Dosimetry Gmbh Due...
The Issue: When the electric lift table is connected to the mains power, in a very rare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-i Anesthesia System Product Usage: The indication for the Flow-i...
The Issue: Electrical issues in the control, monitoring or panel sub-systems, caused by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crazy about Cookies 2lb HELLO KITTY COLLECTION Decorated SUGAR COOKIE...
The Issue: Pre-portioned sugar cookie dough contains undeclared milk and pre-portioned...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Crazy about Cookies 2lb Holiday Gathering COLLECTION Decorated SUGAR COOKIE...
The Issue: Pre-portioned sugar cookie dough contains undeclared milk and pre-portioned...
Recommended Action: Do not consume. Return to store for a refund or discard.