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.
Possible inner labeling and packaged device not matching the outer label on the box.
Issue 1: The MedNet Meds 6.1 and 6.21 programs, under certain conditions, can change the piggyback medication entry set settings for existing defined medication entries. This includes (a)…
For the Fukuda Denshi patient monitor model DS-8100, in less than 0.003% (17) of the 6227 devices sold worldwide, a Short-term Battery Error message has appeared and has been traced back to…
Contraindication language updated in the Instructions For Use (IFU) to indicate that Pentaray Catheters should not be used in patients with prosthetic valves.
Device does not produce a visual or audible impedance respiration APN alarm when an impedance respiration apnea event occurs.
Distribution of unapproved devices with incorrect air compression level setup
Potential unexpected movement of robot arm
The firm received reports of two breakages of the pin tips which occurred during two identical surgery procedures. The breakage occurred at the very distal end of the conical part of the…
Possible inner labeling and packaged device not matching the outer label on the box.
Generator may inadvertently deliver RF energy if the foot pedal is placed in close proximity and oriented toward the Stereotaxis magnets.
Certain iOS and Android App versions contain a program error (bug) in the Bolus Advisor feature. After pairing a meter with the app for the first time, a customer may encounter the rare…
Listeria monocytogenes contamination of non-sterile plated media
A defect in the wire-reinforced tubing may result in a partial of total occlusion when the cuff is over-inflated.
Custom surgical kits contain Aplicare Povidone Iodine Prep Pads which were subsequently recalled by Medline Industries for incorrect expiration date.
A small number of batches may crack or break if exposed to certain chemicals, like certain cleaning agents.
The imported products were found to contain undeclared milk (casein) based on analyses by the Canadian Food Inspection Agency (CFIA).
The firm had a deviation from the Standard of Procedure in the manufacture of Clover Hill Dairy, Soft Ricotta. The facility was temporarily storing whey in a raw milk silo, without cleaning…
Juanita 's Brand OJOS Mexican Pastry, 6 counts in plastic bag, is recalled due to undeclared coconut.
Foreign Matter (a 1/8 long x 8mm, white & blue strand) was found on the product.
Firm received reports of flexible pieces of yellow plastic found in Fit & Active Chocolatey Chip Protein Meal Bars.
Plow and Hearth was notified by a manufacture of their product labeled as chocolate covered cashews were actually salted peanuts. The firm has decided to initiate a recall of the product.…
The imported products were found to contain undeclared milk (casein) based on analyses by the Canadian Food Inspection Agency (CFIA).
Virginia Diner, Inc. is initiating a voluntary recall of Chocolate Covered Cashews that were placed in 60 cans and sold to one direct account because of mislabeling and peanuts were found…
The imported products were found to contain undeclared milk (casein) based on analyses by the Canadian Food Inspection Agency (CFIA).
Browse recent months with enough recall history for useful comparison.
