CareFusion 303 BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software recall — FDA Z-1304-2025
Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).
Complete FDA and NHTSA recall records dated in March 2025.
These records include useful source details for the selected month.
Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Damage to the sterile barrier pouch of catheter, which could potentially compromise its sterility.
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
Unexpected loose material in the male luer used in the aortic root cannula has been identified. Potential harms when identified prior to use - procedure delay. Potential harm if not…
Increase in complaints concerning "pullwire" breakage that may result in the broken pullwire remaining in the anchor implant body after deployment.
Nissan North America, Inc. (Nissan) is recalling certain 2025 Murano, Pathfinder, and INFINITI QX60 vehicles. One or both front brake caliper assemblies may have reduced strength and could…
Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
Product may contain incorrect salad dressing, resulting in fish and wheat being undeclared.
Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
The firm received complaints of spoilage and illness with the use of the products.
Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
Undeclared egg
Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
The firm received complaints of spoilage and illness with the use of the products.
Undeclared almonds
Elevated levels of MBC (carbendazim) thiophanate-methyl.
Undeclared wheat and egg
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.