Abbott Removes Power Cord Associated with HeartMate Mobile Power Unit

by Pill Pals Customer Service | Aug 29, 2025 | News

This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it.  Affected ProductProduct Name: AC Power Cord (model:...

Ambu Removes SPUR II Resuscitators Due to Blocked Manometer Port

by Pill Pals Customer Service | Aug 29, 2025 | News

This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it. Affected Product What to DoDo not use Ambu SPUR II...

Green Lumber Holding, LLC Issues Consumer Alert on Counterfeit Products Following FDA Findings

by Pill Pals Customer Service | Aug 29, 2025 | News

Summary Company Announcement Date: August 28, 2025 FDA Publish Date: August 29, 2025 Product Type: Drugs Reason for Announcement: Recall Reason Description Undeclared prescription drug-Tadalafil Company Name: Green Lumber Holding, LLC. Brand Name: Product Description:...

DermaRite Industries Expands Voluntary Nationwide Recall Due to Potential Burkholderia cepacia Contamination

by Pill Pals Customer Service | Aug 28, 2025 | News

Summary Company Announcement Date: August 27, 2025 FDA Publish Date: August 28, 2025 Product Type: Drugs Reason for Announcement: Recall Reason Description Device & Drug Safety – Potential Burkholderia cepacian contamination Company Name: DermaRite...

Aquastar (USA) Corp Recalls Cocktail Shrimp 6oz Because of Possible Health Risk

by Pill Pals Customer Service | Aug 28, 2025 | News

Summary Company Announcement Date: August 28, 2025 FDA Publish Date: August 28, 2025 Product Type: Food & Beverages Shellfish Contaminants Reason for Announcement: Recall Reason Description Potential Contaminant – cesium-137 (Cs-137) Company Name: Aquastar Corp...

Recall: Integra LifeSciences Recalls Extended Tip Applicator

by Pill Pals Customer Service | Aug 28, 2025 | News

This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it.Affected ProductCatalog NumberProduct Name...