Philips Achieva 3.0T, Magnetic Resonance System recall — FDA Z-1553-2024
Patient support table floor plate may be incorrectly installed.
Complete FDA and NHTSA recall records dated in 2024, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
Patient support table floor plate may be incorrectly installed.
Patient support table floor plate may be incorrectly installed.
Patient support table floor plate may be incorrectly installed.
Specific lots of Neria Soft Infusion Sets, which have been shipped into the US Market, have been shipped with the incorrect Instruction for Use (IFU) within the final pack. The IFU included…
Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
Patient support table floor plate may be incorrectly installed.
Salmonella contamination
Product recalled due to the presence of yellow oleander and its components in the product.
Undeclared allergen milk (whey) and undeclared lard
Product recalled due to the presence of yellow oleander and its components in the product.
Foreign material (metal) in donuts
Sea Salt Almond Allegator candy has a back label for chocolate covered cherries.
Product recalled due to the presence of yellow oleander and its components in the product.
Product recalled due to the presence of yellow oleander and its components in the product.
Foreign material (metal) in donuts
Product recalled due to the presence of yellow oleander and its components in the product.
Product recalled due to the presence of yellow oleander and its components in the product.
Product recalled due to the presence of yellow oleander and its components in the product.
Product recalled due to the presence of yellow oleander and its components in the product.
Product recalled due to the presence of yellow oleander and its components in the product.
Product has been recalled because it may exceed FDA guidance levels for leachable lead.
Coconut is declared in the ingredient list, but not declared in the contains statement in coconut paste.
Product recalled due to the presence of yellow oleander and its components in the product.
Product recalled due to the presence of yellow oleander and its components in the product.
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.