Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
The first time an operator selects a new procedure type during a single examination,the shutter position resets to the open position for the new procedure type. If the shutters had…
The placing of weight on the VRAD detector, of the Brivo XR385 digital radiographic system, can introduce image artifacts, which can result in patient exam retakes.
The diameter of the drill sleeve guide raw material was found to be under tolerance, potentially resulting in the drill bit seizing in the guide during surgery.
A review of product complaints in 2010 identified a trend for the Coring Removal Drill of premature wear and/or breakage. This recall occurred in 2013.
The CryoLife L6318 (Label, BioGlue 12mm Spreader Tip, Indicator Label 2 1/8" x 1 1/4") was incorrectly applied to the Syringe Applicator Tip pouches and Syringe Spreader Tip pouches were…
Two lots of femoral stems were labeled as Size 11. However, they are actually Size 12. Potential adverse effects include poor joint mechanics, improper fit, loosening, and additional…
It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. This may cause media to leak out of the primary sterile packaging…
It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. This may cause media to leak out of the primary sterile packaging…
Possibility that the retaining ring in the 2M inlay 15degree for MUTARS RS Cup and LUMiC TiN is incorrectly mounted.
During manual LAO/RAO rotation at maximum speed or a combination of LAO/RAO and Cran/Caud rotation at maximum speed, the possibility exists for the safety monitoring within the system…
Abbott is advising customers that a small number of CardioMEMS(R) Hospital Electronics Systems (Model CM3000) and Patient Electronics Systems (Model CM1100) may deliver a system error,…
An improper wiring connection on the chiller assembly may result in overheating of the connection and potential failure of certain components in the system.
The product label has missing information, such as the lot number and expiration date, as well as other information.
The main vial label lists the incorrect part number, but the cap label is correct.
Potential to contain metal fragments
Whey powder may have the potential to be contaminated with Salmonella.
This recall has been identified due to the detection of cyclamates (artificial sweetener). Use of or consumption of cyclamates may include potential health hazard. Cyclamates and its salts…
This recall has been identified due to the detection of cyclamates (artificial sweetener). Use of or consumption of cyclamates may include potential health hazard. Cyclamates and its salts…
an ingredient in this product was manufactured during the time-frame and on the same piece of equipment that was associated with a salmonella outbreak.
It was discovered that a bulk salad kit was produced using the wrong components. Instead of cashews, peanuts were packed for the kit
Product labeling does not list milk in the contains statement; however milk is listed as in ingredient.
This recall has been identified due to the detection of cyclamates (artificial sweetener). Use of or consumption of cyclamates may include potential health hazard. Cyclamates and its salts…
Potential to contain metal fragments
Product is decomposed.
Browse recent months with enough recall history for useful comparison.
