95,075 total recalls in our database
Seggiano Usa
The Tuscan Kale Pesto was mislabeled as Seggiano Artichoke & Garlic Sauce & Spread and therefore, contains undeclared cashews.
Schmidt Baking Co.
Schmidt Baking Company has decided to initiate a recall of various bread products, after being informed by one of their vendors that the ingredient supplied to them by the vendor is under recall. Potential of foreign material in product.
Schmidt Baking Co.
Schmidt Baking Company has decided to initiate a recall of various bread products, after being informed by one of their vendors that the ingredient supplied to them by the vendor is under recall. Potential of foreign material in product.
Subpotent Drug: product not meeting the iodine assay level requirements through the labeled expiry.
Non-sterility: confirmed microbial contamination with Achromobacter xylosoxidans
Presence of Foreign Tablet/Capsule; cartons labeled to contain Acyclovir tablets may contain Torsemide tablets in some of the blister cavities.
Presence of Particulate Matter; contains visible particulate matter identified as mold.
Microbial contamination of Non-Sterile Product; product contamination with yeast and mold (Paecilomyces saturatus and Aspergillus fumigatus).
Failed Stability Specifications: Product stability testing results did not meet specifications for iron content.
Presence of Particulate Matter: Customer complaint of particulate matter which has been identified as polyethylene, which is consistent with the material used to manufacture the container cap was received.
Subpotent Drug: Out of specification for an active ingredient cysteamine hydrochloride.
There is an increase in the failure rate of certain Anode Drive Units (ADU5) used in these products. Early life failure of the ADUs only occurs when the hospital mains provide 480V to the system. This current voltage may lead to saturation and overheating of the coils that protect the IGBTs (insulated-gate bipolar transistor) of the ADU. The overheating may also generate a peculiar burning smell that may be noticed. In some instances this burning smell may be noticed before the ADU fails. When the ADU fails the X-ray performance of the system is reduced to Emergency Fluoroscopy. Exposure will not be possible and image quality is reduced.
On June 15, 2017, STERIS identified that the purple ink located on the outside label of Vis-U-All Pouches may migrate following steam processing causing cosmetic defects on the exterior of the pouch and in some instances, transference of the ink onto the device(s) contained within the pouch.
Product packaged in a syringe that is not a lure lock syringe and the tip cold come off when expressing the material.
A faulty footswitch may result in unintended ultrasonic fragmentation activation. There are two scenarios when the failure mode may occur: 1) Ultrasonic fragmentation may be inadvertently activated at start-up or at the initial use once the footswitch is connected to the console and after the user primes the system, performs a handpiece test, and enters the Main Screen. 2) Ultrasonic fragmentation may remain activated during surgical use once the foot pedal is disengaged slowly.
Siemens Medical Solutions USA
Potential for liquid entry
An 8mm diameter bone tap was laser marked as 7mm diameter and was packed with a 7mm label.
Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or inconsistent flow rates.
Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.