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. 961 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
961 in last 12 months

Showing 30041–30060 of 48,330 recalls

DrugFebruary 17, 2017· Pharmedium Services, LLC

Recalled Item: VANCOMYCIN HCl 1.75g in 300 mL 0.9% Sodium Chloride Injection USP Recalled...

The Issue: Labeling: Not Elsewhere Classified: Incorrect volume printed on the product...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2017· Pharmedium Services, LLC

Recalled Item: Potassium PHOSphate added to 0.9% Sodium Chloride Recalled by Pharmedium...

The Issue: Labeling: Not Elsewhere Classified: Incorrect volume printed on the product...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 17, 2017· Pharmedium Services, LLC

Recalled Item: Potassium PHOSphate added to 0.9% Sodium Chloride Recalled by Pharmedium...

The Issue: Labeling: Not Elsewhere Classified: Incorrect volume printed on the product...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 17, 2017· Pharmedium Services, LLC

Recalled Item: Potassium CHLORide added to 0.9% Sodium Chloride Recalled by Pharmedium...

The Issue: Labeling: Not Elsewhere Classified: Incorrect volume printed on the product...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 17, 2017· Pharmedium Services, LLC

Recalled Item: Potassium PHOSphate added to 0.9% Sodium Chloride Recalled by Pharmedium...

The Issue: Labeling: Not Elsewhere Classified: Incorrect volume printed on the product...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Hips Active Articulation ArComXL Bearings...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Custom parts Product Usage: Custom Recalled by...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Extremities Recalled by Zimmer Biomet, Inc....

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants BIO PLUG 10MM Product Usage: Non-weight...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Knees Revision Tibial Tray Systems Oxford...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Sports Med Repicci II Tibial Components...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2017· Merit Medical Systems, Inc.

Recalled Item: 7F Prelude¿ Short Sheath Introducer. Catalog Numbers: K15-00070 Recalled by...

The Issue: Merit Medical Systems, Inc. announces a voluntary field action for sheaths...

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

Class I — Serious Health HazardOngoing
DrugFebruary 16, 2017· Organic Herbal Supply

Recalled Item: XtraHRD Natural Male Enhancement Capsules Recalled by Organic Herbal Supply...

The Issue: Marketed without an Approved NDA/ANDA: Product contains N-desmethyl...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 16, 2017· Allegiant Health

Recalled Item: HealthA2Z CHEWABLE Aspirin (NSAID) 81 mg Recalled by Allegiant Health Due to...

The Issue: cGMP deviations - presence of rubber particles found loose in the bulk product.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2017· Pharmedium Services Llc

Recalled Item: Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Recalled by Pharmedium...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

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

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zenatane (isotretinoin) capsules Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed dissolution specifications - low dissolution results at S3 stage.

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

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2017· Pharmedium Services Llc

Recalled Item: Bupivacaine HCl 0.25% 400 mL Total Volume in an ON-Q Recalled by Pharmedium...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

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

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2017· Pharmedium Services Llc

Recalled Item: Ropivacaine HCl 0.2% 550 mL Total Volume in an AutoFuser Recalled by...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

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

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zenatane (isotretinoin) capsules Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed dissolution specifications - low dissolution results at S3 stage.

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

Class III — Low RiskOngoing
Refund
DrugFebruary 15, 2017· AVKARE Inc.

Recalled Item: Famciclovir tablets Recalled by AVKARE Inc. Due to Failed impurities/...

The Issue: Failed impurities/ degradation specifications: Product was above...

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

Class II — Potential Health HazardOngoing
Refund