Medicines & devicesClass II
American Health Packaging recalls Metoclopramide Tablets
Presence of Foreign Tablets/Capsules
· FDA · Nationwide
Recalls
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 2, 12:57 PM ET · refreshed about every 2.5 hours · RSS · Get recall alerts
FDA drug and medical device recalls.
State filter: shows recalls whose official distribution lists that state, plus nationwide ones. CPSC and NHTSA recalls apply nationwide.
482 recalls
Medicines & devicesClass II
Zydus Pharmaceuticals (USA) Inc recalls Hydrocortisone Sodium Succinate for Injection
Failed Impurities/Degradation Specifications.
· FDA · Nationwide
Medicines & devicesClass II
Teva Pharmaceuticals USA, Inc recalls Metoclopramide Tablets
Presence of Foreign Tablets/Capsules
· FDA · Nationwide
Medicines & devicesClass II
Preferred Pharmaceuticals, Inc. recalls Lidocaine Ointment USP
Failed Content Uniformity Specifications
· FDA · Nationwide
Medicines & devicesClass II
Houston Rx LLC recalls 2 products
Lack of assurance of sterility. Lack of process control
· FDA · Nationwide
Medicines & devicesClass III
SUN PHARMACEUTICAL INDUSTRIES INC recalls 3 products
Failed Impurities/Degradation Specifications
· FDA · Nationwide
Medicines & devicesClass II
INTEGRATED MEDCRAFT LLC recalls FORWARD Gunshot Wound Kit
Subrecall of a kitted device from SafeGuard Medical due to internal testing identified an issue affecting the device's sterile pad, potentially causing the sterile pad to degrade over time. The degradation may cause remn
· FDA · Nationwide
Medicines & devicesClass II
Apothecary Pharma LLC recalls 2 products
Lack of Assurance of Sterility
· FDA · Nationwide
Medicines & devicesClass II
J&J INNOVATIVE MEDICINE recalls IMAAVY (nipocalimab-aahu) Injection
Presence of particulate matter.
· FDA · OH
Medicines & devicesClass II
Apotex Corp. recalls Paroxetine Extended-Release Tablets
Failed dissolution specifications.
· FDA · Nationwide
Medicines & devicesClass II
Steris Corporation recalls HexaVue Focus Integration System
A software issue may result in unintended mismatch of patient information on manually printed images. Incorrect patient information appearing on printed images could create a documentation discrepancy or incorrect associ
· FDA · Nationwide
Medicines & devicesClass II
Steris Corporation recalls 3 products
If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid chemistry may escape from the bottle when the cap is twisted during
· FDA · Nationwide
Medicines & devicesClass II
Cipla USA, Inc. recalls Fosfomycin Tromethamine Granules for Oral Solution
Failed Impurities/Degradation Specifications
· FDA · Nationwide
Medicines & devicesNot Yet Classified
Aurobindo Pharma USA Inc recalls amazon
Discoloration: consumer complaints received for discolored tablets
· FDA · Nationwide
Medicines & devicesClass II
Aurolab Trust recalls FOCUS PI Hypromellose 0
Lack of Assurance of Sterility
· FDA · VA
Medicines & devicesClass II
Ajanta Pharma USA Inc recalls Ranolazine Extended-Release Tablets
Failed Dissolution Specifications: below specification
· FDA · Nationwide
Medicines & devicesClass II
Howmedica Osteonics Corp. recalls 4 products
Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual mo
· FDA
Medicines & devicesClass II
Cook Incorporated recalls Williams Cystoscopic Injection Needles
The female Luer lock adapter component in the affected device lots may not have been correctly seated due to misalignment and inadequate torquing during manufacturing. Potential events that may occur as a result of this
· FDA · FL, IL, NM, TX, WA
Medicines & devicesClass II
Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company recalls 2 products
Lack of Assurance of Sterility
· FDA · Nationwide
Medicines & devicesClass II
Baxter Healthcare Corporation recalls Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Code: 3122005 Product
Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift strap lowers more quickly than expected during use. Patients a
· FDA · Nationwide
Medicines & devicesClass II
NOXBOX LTD recalls NOxBOXi Nitric Oxide Delivery System
Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxygen sensors.
· FDA · Nationwide
Medicines & devicesClass II
K.C. Pharmaceuticals, Inc. recalls 8 products
Lack of Assurance of Sterility
· FDA · Nationwide
Medicines & devicesClass II
Medline Industries, LP recalls Medline convenience kit labeled as: FOOT ANKLE
Discrepancy in the shelf-life of a component
· FDA · Nationwide
Medicines & devicesClass II
Carolina Infusion, LLC recalls 16 products
Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product. Lack of Assurance of Sterility: Related to processing equipment used in compoun
· FDA · Nationwide
Medicines & devicesClass II
Boston Scientific Corporation recalls NaviFlex LW Pusher
Device was incorrectly manufactured with a guidewire exit port (referred to in the IFU as the RX port), which is not a design feature associated with this device configuration.
· FDA · Nationwide
Medicines & devicesClass II
In2bones USA, LLC recalls REF: P65 ST862 CoLag SCREW
Due to labeling error, bone screws specified as fully threaded, are actually partially threaded screws.
· FDA · Nationwide
Medicines & devicesClass II
Amneal Pharmaceuticals, LLC recalls Estradiol Gel
Defective Container; packets were found to be either empty or partially full.
· FDA · Nationwide
Medicines & devicesClass II
Par Health USA, LLC recalls Buprenorphine Hydrochloride
Crystallization
· FDA · Nationwide
Medicines & devicesClass II
Ethicon, LLC recalls PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical Suture
Silk sutures, indicated for use in cardiovascular, ophthalmic and neurological procedures, packaged with alcohol-based fluid, not part of product design, that if discovered prior to use may cause surgical delay. If used,
· FDA · Nationwide
Medicines & devicesClass II
Nihon Kohden America LLC recalls Product Name: Nihon Kohden CNS-6200 Series Central Nurse Station
Due to a cybersecurity issue associate with a NULL Pointer Dereferences vulnerabiity. If exploited would potentially cause disruption of the centralized monitoring of multiple beds and the visualization of alarms.
· FDA · Nationwide
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.