Complete FDA and NHTSA recall records dated in January 2022.
These records include useful source details for the selected month.
Wireless foot switch connection issues causing interruption of Fluoroscopy and exposure
Stems may have an undersized spigot bore diameter therefore separating the proximal body from the stem may not be possible without surgical delay and/or bone damage
A potential chemical degradation of Sevoflurane by Lewis acids (metal oxides and metal halides) has been discovered that may result in inhalation and/or skin exposure of hydrogen fluoride.
Due to dose discrepancy when delivering a plan to a patient in a Non-HFS (Head First Supine) orientation specifically in Feet First Supine (FFS).
Customers reported that the device jaws were difficult to open or would not open following application on tissue. Use of a device with this potential assembly issue could result in the…
When a measurement with a PTW detector array is performed with the software BeamAdjust 2.2 or VeriSoft 8.0, a measurement error can occur under specific conditions. This error can lead to a…
Abnormal images such as horizontal stripes may be displayed and recovery may not not be possible by restarting the system. The worst case scenario is an operator who is working without a…
Stems may have an undersized spigot bore diameter therefore separating the proximal body from the stem may not be possible without surgical delay and/or bone damage
Proton Therapy System (PTS) software can be started in the clinical environment (clinical user) while some processes are still running in the test environment (tcs user). Initiating the…
Stems may have an undersized spigot bore diameter therefore separating the proximal body from the stem may not be possible without surgical delay and/or bone damage
Increase in premature device failures
This recall has been initiated to provide a labeling update with revised instruction how to operate the unit with Cold Therapy pads.
(1)Start-up problem: Intermittently at start-up of the system, the communication of the control unit that manages the movement of the stand is not established; (2) Emergency stop recovery…
There is a high risk of the blue hub detaching from the corkscrew needle, resulting the the needle remaining in the patient's scalp.
Stems may have an undersized spigot bore diameter therefore separating the proximal body from the stem may not be possible without surgical delay and/or bone damage
Stems may have an undersized spigot bore diameter therefore separating the proximal body from the stem may not be possible without surgical delay and/or bone damage
Product is labeled as non-pyrogenic but endotoxin testing was not performed.
During an FDA investigation the firm was notified that the product contains undeclared milk.
During an FDA investigation the firm was notified that the product contains undeclared milk.
During an FDA investigation the firm was notified that the product contains undeclared milk.
Undeclared Wheat, Milk, Egg, Soy, or Sesame on retail packaged bread products due to no ingredient statements.
During an FDA investigation the firm was notified that the product contains undeclared shellfish.
Undeclared Wheat, Milk, Egg, Soy, or Sesame on retail packaged bread products due to no ingredient statements.
During an FDA investigation the firm was notified that the product contains undeclared milk.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
