95,114 total recalls in our database
Tradewind Foods de Puerto Rico
Goya de Puerto Rico is recalling the following products due to a possible can seam defect that may compromise the integrity of the product.
Tradewind Foods de Puerto Rico
Goya de Puerto Rico is recalling the following products due to a possible can seam defect that may compromise the integrity of the product.
Tradewind Foods de Puerto Rico
Goya de Puerto Rico is recalling the following products due to a possible can seam defect that may compromise the integrity of the product.
Tradewind Foods de Puerto Rico
Goya de Puerto Rico is recalling the following products due to a possible can seam defect that may compromise the integrity of the product.
Presence of Particulate Matter: particulate matter was found during the manufacturing process.
Presence of Particulate Matter: Confirmed customer complaint of discolored solution with visible metal particles embedded in the glass vial and visible in the solution.
Actavis Laboratories, FL
Failed Tablet/Capsule Specifications: Recall due to complaints of split or broken tablets.
Lack of Assurance of Sterility; leaking of premix bags
Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.
Baxter Healthcare
Lack of Assurance of Sterility: A small cut in the solution bag may have been introduced during the manufacturing process, resulting in a leak of the bag into the overpouch.
New England Home Therapies
Lack of Assurance of Sterility: All compounded products.
Presence of Foreign Tablets/Capsules; Presence of co-mingled LipaCreon 13000.
Eugene Oregon
Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.
Eugene Oregon
Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.
Actavis Laboratories, FL
Failed Tablet/Capsule Specifications: Recall due to complaints of split or broken tablets.
Cubist Pharmaceuticals
Presence of Particulate Matter: Potential presence of glass particulate matter in the vials.
Ingenuity CT system can mislabel the exposure that results in an image in the incorrect order that it was taken by the user.
Two malfunctions posing potential risk to patients were identified with Siemens Ysio Max, AXIOM Luminos dRF Max, Uroskop Omnia Max, and Luminos Agile Max systems with a specific set of serial numbers that will cause lost images due to an automatic Radiology Information System (RIS) worklist update, thus causing examinations to be repeated. Image label may also be displayed incorrectly after images
Additional caution statements have been added to the Instructions For Use for monopolar electrodes. 1) To avoid tissue carbonation, the operation voltage of the HF generator must not exceed 650 peak voltage (Vp) for all monopolar electrodes. and 2) For all monopolar electrodes, the useful life of this product is less than or equal to 50 cycles and less than or equal to 2 years.
Additional caution statements have been added to the Instructions For Use for monopolar electrodes. 1) To avoid tissue carbonation, the operation voltage of the HF generator must not exceed 650 peak voltage (Vp) for all monopolar electrodes. and 2) For all monopolar electrodes, the useful life of this product is less than or equal to 50 cycles and less than or equal to 2 years.