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. 1,747 recalls have been distributed to Delaware in the last 12 months.
Showing 34881–34900 of 48,330 recalls
Recalled Item: SyrSpend SF Recalled by Fagron, Inc Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rocuronium Bromide 50 MG/5ML INJ. Recalled by RemedyRepack Inc. Due to...
The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Humulin 70/30 Recalled by RemedyRepack Inc. Due to Labeling: Incorrect...
The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SyrSpend SF Recalled by Fagron, Inc Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novolin 70/30 Recalled by RemedyRepack Inc. Due to Labeling: Incorrect...
The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam 2 mg/mL Inj. Recalled by RemedyRepack Inc. Due to Labeling:...
The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SyrSpend SF Recalled by Fagron, Inc Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ascorbic Acid 500 MG/ML Inj. Recalled by RemedyRepack Inc. Due to Labeling:...
The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prednisone 20 mg Recalled by Northwind Pharmaceuticals LLC Due to Labeling:...
The Issue: Labeling: Not elsewhere classified. NDC number is incorrect on the container.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PerCoBa 1 Recalled by Immuno - Dynamics, Inc Due to The PerCoBa brand and...
The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PerCoBa Whey Protein Isolate with Colostrum Recalled by Immuno - Dynamics,...
The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Colostrum Lozenges Recalled by Immuno - Dynamics, Inc Due to The PerCoBa...
The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PerCoBa Colostrum Capsules Recalled by Immuno - Dynamics, Inc Due to The...
The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Colostrum Powder Recalled by Immuno - Dynamics, Inc Due to The PerCoBa brand...
The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips Healthcare DigitalDiagnost stationary X-ray system Recalled by...
The Issue: The detector may signal that it is ready for acquisition when it actually is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DuraDiagnost stationary X-ray system Recalled by Philips...
The Issue: The detector may signal that it is ready for acquisition when it actually is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reagent Management System (RMS) Dimension RxL Max HM STM Product Recalled by...
The Issue: Siemens has identified RMS compressors that are missing the safety cover on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniAxial Pedicle Screw & UniAxial Reduction Pedicle Screw The Response...
The Issue: Response Spine UniAxial Pedicle & UniAxial Reduction Pedicle Screws may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Screw Driver SJ706R Recalled by Aesculap, Inc. Due to The flexible...
The Issue: The flexible shaft of the instruments may break during orthopedic spinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Bone Awl Recalled by Aesculap, Inc. Due to The flexible shaft of...
The Issue: The flexible shaft of the instruments may break during orthopedic spinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.