Complete FDA and NHTSA recall records dated in March 2024.
These records include useful source details for the selected month.
Due to two complaints, has come to our attention that additional guidance is required on the correct interpretation of the carton label Size and Type columns to avoid misinterpretation…
Siemens Healthcare Diagnostics has confirmed an average negative bias of -35% compared to the 3rd World Health Organization (WHO) International Standard (NIBSC code: 11/170) that is…
Due to two complaints, has come to our attention that additional guidance is required on the correct interpretation of the carton label Size and Type columns to avoid misinterpretation…
The needle cannula of a retractable needle may detach from the needle holder in the patient.
Due to two complaints, has come to our attention that additional guidance is required on the correct interpretation of the carton label Size and Type columns to avoid misinterpretation…
Siemens Healthcare Diagnostics has confirmed an average negative bias of -35% compared to the 3rd World Health Organization (WHO) International Standard (NIBSC code: 11/170) that is…
Medos has received an increase in complaints for CEREBASE DA Guide Sheath with reports of fractures at the distal end, which may result in surgical procedural delay, vascular injury and in…
Due to a manufacturing issue, device under process validation phase were inadvertently mixed into the main manufacturing process.
Retroactively reported corrections from 2023: 1) A software defect may cause an incorrect (Fail-Stop) alarm when an administration set is loaded or coupled while the pump is executing the…
Pack and pouch label is missing the manufacturing and expiration date.
Due to two complaints, has come to our attention that additional guidance is required on the correct interpretation of the carton label Size and Type columns to avoid misinterpretation…
Retroactively reported correction from 2022: A software defect may cause an incorrect (Fail-Stop) Alarm when an administration set is loaded with an upstream occlusion present, resulting in…
The product is labeled as Chocolate Cake. However, the packaging contains slices of carrot cake. The Carrot Cake contains soy which is not listed in the ingredient or allergen contain…
Potential cross contact with sesame.
Undeclared sesame.
Potential cross contact with sesame.
Undeclared sesame.
Product ingredient may be contaminated with Listeria monocytogenes.
Undeclared allergens FD&C Yellow #5, Yellow #6
potential allergen contact with almonds, pecans and coconut.
Potential cross contact with sesame.
Potential cross contact with sesame.
The product is labeled as Carrot Cake on the top but the ingredient panel on the bottom is for Chocolate Cake. The Chocolate Cake ingredient statement does not include soy which is in the…
Kia America, Inc. (Kia) is recalling certain 2020-2024 Telluride vehicles. The intermediate shaft and right front driveshaft may not be fully engaged, which can result in vehicle roll away…
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.
