Teleflex Medical Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079 recall — FDA Z-1829-2017
Some of the individual unit packaging (pouches) may be missing the lot number an expiration date.
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.
Some of the individual unit packaging (pouches) may be missing the lot number an expiration date.
During internal testing, Neodent determined that the body diameter (3.8mm) of the Neodent 108.139 CM Exact Intraoral Scan body is not compatible with the platform diameter of CM Implants…
Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming
The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling.
Due to a leak in the detector cooling system, cooling liquid may leak outside the drip tray of the chiller. If this occurs the liquid may drip onto electrical components in the R cabinet…
BD has confirmed reports that lower than expected RFU values were generated on customer BD Viper LT Systems after the installation of software version 3.00H. As RFU values decrease, results…
Endotoxin levels higher than process maximum limits were discovered in the identified polyethylene components.
Mizuho has discovered that the 5319-37 Wilson Frame Pads have a design deficiency in the construction of their mounting sleeves that may allow the patient to contact the underlying carbon…
Beckman Coulter is recalling the Access Ferritin Calibrators kit because it contains a calibration card with an incorrect S5 calibrator concentration.
The BD MAX System software version 4.44A contains a software anomaly that has the potential to affect some Open System Reagent (OSR) customers utilizing User Defined Protocol (UDP) assays.…
The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling.
Endotoxin levels higher than process maximum limits were discovered in the identified polyethylene components.
Product has the potential to be contaminated with Salmonella.
Product has the potential to be contaminated with Salmonella.
Product has the potential to be contaminated with Salmonella.
Product has the potential to be contaminated with Salmonella.
Product has the potential to be contaminated with Salmonella.
Product has the potential to be contaminated with Salmonella.
Possible contamination with E. coli O157
Product has the potential to be contaminated with Salmonella.
Product has the potential to be contaminated with Salmonella.
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
Product has the potential to be contaminated with Salmonella.
Product may be contaminated with listeria monocytogenes
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