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. 1,677 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,677 in last 12 months

Showing 4294142960 of 48,330 recalls

DrugSeptember 23, 2013· Tolmar, Inc.

Recalled Item: Ketoconazole Shampoo Recalled by Tolmar, Inc. Due to Subpotent

The Issue: Subpotent

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

Class III — Low RiskOngoing
Refund
DrugSeptember 23, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: Irinotecan Hydrochloride Injection Recalled by West-Ward Pharmaceutical...

The Issue: Superpotent Drug: a recent review of the USP revealed that an incorrect...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: Irinotecan Hydrochloride Injection Recalled by West-Ward Pharmaceutical...

The Issue: Superpotent Drug: a recent review of the USP revealed that an incorrect...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Alere San Diego, Inc.

Recalled Item: Alere Triage¿ TOX Drug Screen Control 1 Product Generic Name: Recalled by...

The Issue: Alere San Diego, Inc. initiated a voluntary recall of Alere Triage TOX Drug...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Regional Anesthesia Tray with Drugs Recalled by Smiths Medical ASD,...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Saddleblock Tray with Drugs 26g Quincke Recalled by Smiths Medical...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 22g/25g Quincke Recalled by Smiths Medical...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Baylis Medical Corp *

Recalled Item: Baylis Medical TorFlex Transseptal Guiding Sheath Recalled by Baylis Medical...

The Issue: The TorFlex Transseptal Guiding Sheath Kits are being recalled due to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 22g Whitacre/25g Whitacre Recalled by Smiths...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Saddleblock Tray with Drugs  25g Quincke Recalled by Smiths Medical...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Saddleblock Tray with Drugs 22g Quincke (Without Introducer)...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2013· Maquet Cardiovascular, LLC

Recalled Item: Ultima OPCAB System Recalled by Maquet Cardiovascular, LLC Due to MAQUET has...

The Issue: MAQUET has identified a potential issue with the ULTIMA OPCAB (part numbers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2013· Midmark Corp dba Progeny Inc

Recalled Item: The Vantage Digital Panoramic System delivers high-value features standard...

The Issue: An error was identified in the Real Time Controller (RTC) firmware versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2013· Medrad Inc dba Bayer R&I

Recalled Item: MEDRAD¿ Stellant CT Injector System with Certegra Workstation Recalled by...

The Issue: The root cause investigation showed that the under-volume hazard can occur...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2013· Aesculap, Inc.

Recalled Item: Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)...

The Issue: The trial insertion instrument may disassemble during use due to a...

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

Class II — Potential Health HazardOngoing
FoodSeptember 20, 2013· Garden-Fresh Foods, Inc.

Recalled Item: Market Pantry Reduced Fat American Potato Salad Recalled by Garden-Fresh...

The Issue: Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 20, 2013· Garden-Fresh Foods, Inc.

Recalled Item: Finest Traditions Smoky Baked Beans Recalled by Garden-Fresh Foods, Inc. Due...

The Issue: Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip...

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

Class I — Serious Health HazardOngoing
Refund