Complete FDA and NHTSA recall records dated in January 2024.
These records include useful source details for the selected month.
Cardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the products…
Hole(s) to the outer pouch of the Introducer Kits (both trayed and non-trayed) may compromise the sterile barrier of the Introducer Kits. Non-sterile product exposes patients to the…
In rare cases, the lever of the throttle can get temporarily stuck during the movement and does not come back to its neutral point by itself. If this happens during usage, an unwanted…
Instructions for Use-User Deviations related to the reprocessing of the videoscope detailed in the Reprocessing Manual Instructions. The steps are required for the proper reprocessing of…
Daily recommended consumption of Cholesterol and Sodium are listed in grams instead of milligrams. Product content information is accurate.
Undeclared Allergens - Milk and Soy
Undeclared Allergens - Milk and Soy
Daily recommended consumption of Cholesterol and Sodium are listed in grams instead of milligrams. Product content information is accurate.
Undeclared Allergens - Milk and Soy
Undeclared Allergens - Milk and Soy
Undeclared Allergens - Milk and Soy
Undeclared Allergens - Milk and Soy
Daily recommended consumption of Cholesterol and Sodium are listed in grams instead of milligrams. Product content information is accurate.
Undeclared Allergens - Milk and Soy
FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.
Presence of Foreign Tablets/Capsules
Defective Container: powder may leak out of the pouch
The following was missing from the Contraindications Statement: The AVAPS-AE therapy mode is contraindicated for invasive use and patients less than 10 kg. The AVAPS feature is…
A decrease in the reactivity of HSV Type 1/2 lgM in the Serology ToRCH lgM Positive Control when tested on the DiaSorin Liaison XL.
The sterility of microcatheter and infusion system devices cannot be guaranteed.
Spinal fixation system 7.5mmx 50mm screws are packaged with the correct labeling, but the screws themselves were laser marked with an incorrect size description of 7.5 x 40; use of…
Firm is recalling all kits containing recalled lots of Nurse Assist Sterile 0.9% Normal Saline. Nurse Assist identified product in distribution for which the required sterility assurance…
The following features have been disabled from the web-based portal because the FDA has not evaluated these features for safety and effectiveness: Notifications via email feature; AIC alarm…
Firm is recalling all kits containing recalled lots of Nurse Assist Sterile 0.9% Normal Saline. Nurse Assist identified product in distribution for which the required sterility assurance…
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.
