Baxter Healthcare Compella Therapy Air Supply Unit recall — FDA Z-0821-2022
Potential damage to the power cord may cause the power conductors to be exposed, thereby creating a risk of shock from the power mains.
Complete FDA and NHTSA recall records dated in 2022, 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.
Potential damage to the power cord may cause the power conductors to be exposed, thereby creating a risk of shock from the power mains.
Labelled with an incorrect expiry date on the outer label with an extended expiry date than the validated shelf life. The correct expiry date for the device is 2022-02 and not 2023-05 as…
Contains statement declares Fish but does not specify the name of fish.
Packaged of Dark Chococlate Covered Cherries may contain Dark Chocolate covered almonds. Undeclared allergen - tree nuts (almonds).
Flow Beverages Inc., 33 Lakeview CT., Verona, VA, 24482 is initiating a recall of Flow Alkaline Spring Water - Organic lemon & ginger flavored water, 500 ml 12 units per case, Lots…
Thai Noodle Salad Kits is being recalled due to potential foreign material present in an ingredient.
Contains statement declares Fish but does not specify the name of fish.
Contains statement declares Fish but does not specify the name of fish.
Flow Beverages Inc., 33 Lakeview CT., Verona, VA, 24482 is initiating a recall of Flow Alkaline Spring Water - Organic lemon & ginger flavored water, 500 ml 12 units per case, Lots…
Undeclared Coconut in the Contains statement.
Undeclared Egg Allergen
Undeclared Almond and Coconut in the Contains statement.
Potential to contain foreign material (metal).
Firm is recalling Dried Plums due to potential high lead content.
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Product found to be Sub Potent or Exceeded reconstitution time
Sub Potent
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
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.