Recall watch
Supplement recalls from the last 12 months, plus FDA's latest MedWatch safety alerts, pulled from FDA's public data.
20 alerts · covers drugs, medical devices and supplements · updated Oct 13, 2026 3:11pm MST
Certain Medline convenience kits containing recalled BD ChloraPrep applicators should be removed from use due to potential fungal contamination
Read the full notice on FDA.gov →FOR IMMEDIATE RELEASE - ROCHESTER, MI– October 8, 2026 –Par Health is voluntarily recalling two lots of Brevital® Sodium 500 mg/vial CIV (Methohexital Sodium for Injection, USP) to the hospital level. The product is being recalled due to the presence of particulate matter identified as cellulose.
Read the full notice on FDA.gov →A software app or transducer connection problem with the Philips Lumify diagnostic ultrasound system can result in loss of or delays in scanning functionality.
Read the full notice on FDA.gov →WALTHAM, Mass., October 5, 2026 – Nova Biomedical initiated a global Medical Device Correction on July 24, 2026, for the StatStrip® Glucose Hospital Meter System due to a software issue that may cause a glucose result to be associated with the wrong patient. When a patient ID barcode is scanned, pri
Read the full notice on FDA.gov →Black specks and particulate reported in drip chambers of certain ICU Medical IV tubing sets does not affect device safety, performance, or intended use.
Read the full notice on FDA.gov →BD Alaris Pump Infusion Sets are being removed and discontinued; Alaris Pump Module model 8100 has updated performance data
Read the full notice on FDA.gov →Removal of VentStar Resus Neo hoses due to the potential for cracks resulting in restricted ventilation or delayed therapy.
Read the full notice on FDA.gov →IMMEDIATE RELEASE - Tomball, Texas – October 1, 2026 – Greenwich Rx, a 503A compounding pharmacy, is voluntarily recalling specific lots of its compounded glutathione to the consumer level. The product is being recalled due to potential elevated endotoxin levels.
Read the full notice on FDA.gov →Boston Scientific Imager II Angiographic Catheters removed due to a manufacturing issue leading to tip detachment; could result in procedural delays, embolism
Read the full notice on FDA.gov →Abiomed is removing Automated Impella Controllers due to purge cassette recognition failures that may lead to prolonged delayed in mechanical circulatory support.
Read the full notice on FDA.gov →BD is correcting convenience kits and procedural trays containing recalled Huons Co. sodium chloride ampules
Read the full notice on FDA.gov →IFT cable connector on VOCSN devices may become unseated and lose communication with internal flow transducer board leading to reboots, System Fault 10 Alarms.
Read the full notice on FDA.gov →Abiomed is removing certain Impella Controllers with various hardware, firmware, and/or software updates based on a retrospective review of servicing records.
Read the full notice on FDA.gov →The cannula sets may exhibit a loose connection between the flexible tubing and the nasal cannula resulting in reduced effectiveness and decreased oxygenation.
Read the full notice on FDA.gov →Otsuka ICU Medical LLC is issuing a voluntary recall for one lot of 0.9% SODIUM CHLORIDE Injection, USP, 100mL single pack to the user level due to a potential mix-up. The affected lot of 0.9% SODIUM CHLORIDE Injection, USP (NDC: 0990-7984-23 Lot 1042188) may potentially contain the overwrap with la
Read the full notice on FDA.gov →AVID Medical is correcting convenience kits containing recalled Huons Co. sodium chloride ampules.
Read the full notice on FDA.gov →ROCHESTER, MI– September 18, 2026 –Par Health is voluntarily recalling two lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection 400 mcg/100 mL (4 mcg/mL) to the hospital level. The product is being recalled due to the presence of particulate matter identified as cellulose or stopper materia
Read the full notice on FDA.gov →Spectra Medical Devices is removing Sodium Chloride Flush products that were manufactured by Huons Co,. Ltd.
Read the full notice on FDA.gov →The NOxBOX NOxBOXi System may leak oxygen during inhaled nitric oxide therapy
Read the full notice on FDA.gov →The Medtronic and Given Imaging Bravo CF esophageal pH monitoring capsule can fail to attach to the esophagus or detach from its delivery device.
Read the full notice on FDA.gov →Supplement recalls come from openFDA's food enforcement reports, which include dietary supplements, and are shown as FDA published them. We filter for records that mention supplements, so a few may be other products. A recall listed here has nothing to do with PillWatch's verification of any brand. For official notices, see FDA's recalls page. FDA safety alerts come from FDA's MedWatch feed and cover drugs, medical devices and supplements. To report a problem with a supplement, use FDA's Safety Reporting Portal.
This page uses FDA public data but is not endorsed by FDA.
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