Safety recalls that rarely make the news, straight from the official U.S. agency records (FDA, USDA, CPSC, NHTSA). Every listing links to its official notice. We only copy what the record says.
Checked Nov 3, 8:55 PM ET · refreshed about every 2.5 hours · RSS · Get recall alerts
State filter: shows recalls whose official distribution lists that state, plus nationwide ones. CPSC and NHTSA recalls apply nationwide.
1107 recalls
FoodClass IIUpdated
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.
· FDA · 49 states
Medicines & devicesClass II
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
· FDA · Nationwide
FoodPublic Health Alert
Public Health Alert · Public Health Alert
· USDA FSIS · CA, FL, TX
FoodClass I
Product may be contaminated with Salmonella Typhimurium
· FDA · Nationwide
FoodClass I
Undeclared peanuts
· FDA · WA
Medicines & devicesClass II
10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes (VSWVN1010).
· FDA · Nationwide
Medicines & devicesClass II
Pedicle screw system intended to provide immobilization/stabilization of spinal segments as adjunct to thoracic/lumbar/sacral spine fusion may have anti-torque instrument with undersized condition which could prevent mat
· FDA · Nationwide
Medicines & devicesClass I
Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system under certain procedural or anatomical conditions due to a man
· FDA · Nationwide
Medicines & devicesClass II
Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to maintain the cuff pressure set by the user.
· FDA · Nationwide
Medicines & devicesClass IIUpdated
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
· FDA · Nationwide
Medicines & devicesClass IIUpdated
Potential sterile breach of the pouches in which devices are packaged.
· FDA · Nationwide
Medicines & devicesClass IIUpdated
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent
· FDA · Nationwide
Medicines & devicesClass IUpdated
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, whi
· FDA · Nationwide
Medicines & devicesClass IUpdated
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
· FDA · Nationwide
FoodClass II
Foreign material found in product (identified as metal shavings)
· FDA · DE, MD, NJ, NY, PA
Medicines & devicesClass II
The active ingredient concentration in the lysing bag solution of specific GEM Premier 7000 with iQM3 PAK lots did not meet established manufacturing specifications. The malfunction could result in delayed recognition an
· FDA · Nationwide
Medicines & devicesClass II
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
· FDA · Nationwide
Medicines & devicesClass II
Flexible hysteroscopes indicated for use during diagnostic and operative hysteroscopic procedures may contain an expired single use endoscopic seal for gynecology use, which could impact the assurance of sterility.
· FDA · Nationwide
Medicines & devicesClass II
Potential for brush heads to break.
· FDA · Nationwide
Medicines & devicesClass II
Under extended clinical use conditions (e.g., long duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing or at the hydrophobic filter and waterproof pressur
· FDA · Nationwide
Medicines & devicesClass IUpdated
External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus delivery. The primary failure mode is pump under-delive
· FDA · Nationwide
Medicines & devicesClass IIUpdated
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
· FDA · Nationwide
Medicines & devicesClass II
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
· FDA · Nationwide
Medicines & devicesClass II
Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session, the user is not notified of the change.
· FDA · Nationwide
Medicines & devicesClass II
cGMP deviations
· FDA · CA, FL
Medicines & devicesClass II
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 variab
· FDA · Nationwide
Medicines & devicesClass II
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 variab
· FDA · IA, MN, MO
Medicines & devicesClass II
Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage.
· FDA · Nationwide
Medicines & devicesClass II
Due to catheter separation
· FDA · Nationwide
Medicines & devicesClass II
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
· FDA · MN, NC, TX
Recall data comes from official U.S. government sources: openFDA (food, drugs, devices), USDA FSIS (meat, poultry, egg products), CPSC (consumer and children’s products) and NHTSA (vehicles, equipment, car seats). openFDA notes its data should not be relied on for medical decisions. Always confirm with the official notice. Check your vehicle by VIN at nhtsa.gov/recalls.