All Recalls

95,102 total recalls in our database

Firm's dietary supplements were being promoted for conditions that caused the products to be drugs under the FD&C Act.

Jul 31, 2015 Produce View Details →

Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter (human hair).

Jan 28, 2015 Prescription Drugs Nationwide View Details →

Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the aluminum tube and potentially introducing the particle into the product.

Aug 24, 2015 Other Drugs Nationwide View Details →

Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the aluminum tube and potentially introducing the particle into the product.

Aug 24, 2015 Prescription Drugs Nationwide View Details →

Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the aluminum tube and potentially introducing the particle into the product.

Aug 24, 2015 Prescription Drugs Nationwide View Details →

Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter (human hair).

Jan 28, 2015 Prescription Drugs Nationwide View Details →

Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter (human hair).

Jan 28, 2015 Prescription Drugs Nationwide View Details →

Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter (human hair).

Jan 28, 2015 Prescription Drugs Nationwide View Details →

Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter (human hair).

Jan 28, 2015 Prescription Drugs Nationwide View Details →

Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter (human hair).

Jan 28, 2015 Prescription Drugs Nationwide View Details →

Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the aluminum tube and potentially introducing the particle into the product.

Aug 24, 2015 Other Drugs Nationwide View Details →

Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter (human hair).

Jan 28, 2015 Prescription Drugs Nationwide View Details →