Instrumentation Laboratory Co Hemosll ReadiPlasTin (10 mL Size), Part Number 0020301300 recall — FDA Z-0077-2019
There is a potential for increased imprecision, out of range quality controls and prolonged sample results.
Complete FDA and NHTSA recall records dated in October 2018.
These records include useful source details for the selected month.
There is a potential for increased imprecision, out of range quality controls and prolonged sample results.
Bayer has received reports of loose particulate in the filter when the dust cap is removed. Bayer conducted further testing confirming the dust cap may generate particulate which may…
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
Product marketed in U.S. does not have sufficient data to ensure that it will meet the internal burst pressure specifications at the end of 5 yrs shelf-life
Potential for the tethered plug on the hub of the NeoMed Enteral Feeding Tubes with Enteral Only Connectors to inadvertently open after closure.
When multiple CARESCAPEMonitor B450 or B850 units are connected to the same network and a network overload occurs for a prolonged time, the monitors may simultaneously restart as designed.…
The anterior and posterior markers on the cage were on the incorrect/opposite sides of the cage.
Firm received sporadic reports of discoloration on certain lots of the product, which has been identified as common mold.
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
The reason for this field action is due to the mounting of a non-tamper-resistant (ordinary) battery drawer on some BABY440 hearing aids. The correct battery drawer is tamper-resistant and…
Reprocessed Agilis Steerable Introducers may not meet endotoxin requirements per product specification for biological residues determined by LAL testing.
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
The seal of the sterile pouch may be compromised, thereby increasing the risk of infection.
Undeclared wheat and soy lecithin
Incorrect ingredients listed: Does not include Amaranth flour nor baking soda, but does include baking powder and vanilla
Undeclared wheat and soy lecithin
Undeclared wheat, soy lecithin, and milk
Product may contain undeclared milk.
Undeclared wheat, soy lecithin, and milk
Lloyd s Ice Cream of Evansville, IN is voluntarily recalling pre-packed quarts of Reese s Oreo Ice Cream because the product label does not declare peanuts.
Labeling: Not Elsewhere Classified: mislabeling of the Altavera generic name on the packaging component that may cause confusion.
Correct Labeled Product Mispack: confirmed report involving a single unit of properly labeled Heparin in 0.45% Sodium Chloride for Injection (NDC 0409-7651-03, Lot 87903FW) that was found…
CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
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.