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. 1,816 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,816 in last 12 months

Showing 2530125320 of 48,330 recalls

DrugJune 8, 2018· Ingenus Pharmaceuticals Llc

Recalled Item: Irinotecan Hydrochloride Injection Recalled by Ingenus Pharmaceuticals Llc...

The Issue: Superpotent Drug: High out of specification assay value results for potency.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJune 8, 2018· T R Toppers, Inc.

Recalled Item: TR Toppers Brand Chopped Chocolate Pretzel Pieces. Item number B160-075...

The Issue: Recalling TR Toppers Brand Chopped Chocolate Pretzel Pieces due to the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Bio-Rad Laboratories, Inc

Recalled Item: MRSASelect Recalled by Bio-Rad Laboratories, Inc Due to Abnormal coloration...

The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Bio-Rad Laboratories, Inc

Recalled Item: MRSASelect II Recalled by Bio-Rad Laboratories, Inc Due to Abnormal...

The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2018· GE Medical Systems, LLC

Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...

The Issue: The latest on-site software version may not have been reinstalled at some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2018· GE Medical Systems, LLC

Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...

The Issue: The latest on-site software version may not have been reinstalled at some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2018· GE Medical Systems, LLC

Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...

The Issue: The latest on-site software version may not have been reinstalled at some...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJune 6, 2018· Pharmalucence, Inc.

Recalled Item: Kit for the Preparation of Technetium Tc99m Medronate Recalled by...

The Issue: Lack of assurance of sterility: Technetium TC-99M Medronate Kit has a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 6, 2018· GE Medical Systems, LLC

Recalled Item: Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the...

The Issue: GE Medical Systems has discovered a small area on the bore surface of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2018· Tosoh Bioscience Inc

Recalled Item: G8 Automated HPLC Analyzer: HLC-723G8-ST Recalled by Tosoh Bioscience Inc...

The Issue: HbAE is known to interfere with the HbA1c assay on the current version of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...

The Issue: The firm has learned that some RayStation/RayPlan users have commissioned...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJune 5, 2018· PharMEDium Services, LLC

Recalled Item: HYDROmorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride Recalled by...

The Issue: Superpotent and Subpotent

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund