The latest food, drug and medical device recalls reported by the U.S. Food and Drug Administration, newest first. Data updated Oct 21, 2026.
87,918 recalls · page 22 of 30
CGMP Deviations: Potential contamination of raw material
Reported Sep 9, 2026 · D-0829-2026
CGMP Deviations
Reported Sep 9, 2026 · D-0806-2026
Presence of Foreign Tablets/Capsules
Reported Sep 9, 2026 · D-0822-2026
CGMP Deviations
Reported Sep 9, 2026 · D-0809-2026
CGMP Deviations
Reported Sep 9, 2026 · D-0820-2026
CGMP Deviations
Reported Sep 9, 2026 · D-0819-2026
Cross Contamination with Other Products
Reported Sep 9, 2026 · D-0837-2026
Failed Stability Specifications: Out of specification stability result for the protein concentration profile.
Reported Sep 9, 2026 · D-0838-2026
Failed Dissolution Specifications; product failed to meet 18-month stability testing acceptance criteria
Reported Sep 9, 2026 · D-0839-2026
CGMP Deviations
Reported Sep 9, 2026 · D-0818-2026
CGMP Deviations
Reported Sep 9, 2026 · D-0805-2026
CGMP Deviations
Reported Sep 9, 2026 · D-0816-2026
Failed Dissolution Specifications
Reported Sep 9, 2026 · D-0830-2026
Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution
Reported Sep 9, 2026 · D-0847-2026
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding which may extend to the seal area. If the sterile barrier is compromised, patients and users may be exposed to microbial contamination. Potential health consequences may include no injury, localized infection, or, less commonly, more serious infection requiring medical treatment, antimicrobial therapy, procedural intervention, or hospitalization. In rare cases, particularly in critically ill or immunocompromised patients, severe infection could become life-threatening.
Reported Sep 9, 2026 · Z-3057-2026
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.
Reported Sep 9, 2026 · Z-3046-2026
A positive drift in QC values within the reagent's stated 4-hour onboard stability period was identified
Reported Sep 9, 2026 · Z-3047-2026
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.
Reported Sep 9, 2026 · Z-3103-2026
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.
Reported Sep 9, 2026 · Z-3095-2026
Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovolemia.
Reported Sep 9, 2026 · Z-3087-2026
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.
Reported Sep 9, 2026 · Z-3102-2026
Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is encountered during insertion, withdraw cannula and reassess the insertion conditions (i.e. insertion angle, incision size, etc.) before proceeding because forcing the cannula may cause corneal abrasion, iris trauma or descemet's membrane detachment.
Reported Sep 9, 2026 · Z-3064-2026
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.
Reported Sep 9, 2026 · Z-3099-2026
There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed notification of an AF Burden Alert may delay clinical evaluation or therapeutic intervention of an atrial arrhythmia.
Reported Sep 9, 2026 · Z-3081-2026
Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.
Reported Sep 9, 2026 · Z-3043-2026
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.
Reported Sep 9, 2026 · Z-3044-2026
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.
Reported Sep 9, 2026 · Z-3073-2026
Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovolemia.
Reported Sep 9, 2026 · Z-3084-2026
Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.
Reported Sep 9, 2026 · Z-3042-2026
Software issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation or instrument positioning.
Reported Sep 9, 2026 · Z-3088-2026