495 recalls tagged with “suffocation risk”.
B BRAUN MEDICAL INC recalls 5,770 PERIFIX FX Epidural Anesthesia Trays nationwide after a potential lid misalignment in the catheter connector. The issue could affect catheter administration. Stop using the device and follow recall instructions immediately. Healthcare providers should contact B Braun for guidance.
B Braun Medical has an active recall of the PERIFIX FX Continuous Epidural Anesthesia Tray nationwide. The recall cites a potential mispositioned catheter connector lid. Healthcare providers and patients should stop using the device and follow manufacturer instructions.
Taproom Gourmet brand bulk Broadway Mix recall covers 3,547 cases distributed across six states. The recall cites no ingredient label and undeclared allergens including peanuts, sesame, wheat and soy. Consumers should not consume the product and should seek refund or replacement through Egress Capital Partners Inc.
Taproom Gourmet recalled 3,547 cases of 18lb and 20lb bulk Fifth Avenue Mix sold in six states after undeclared peanuts, almonds, cashew, and soy were found. The recall classifies the hazard as HIGH. Consumers should discard the product or return for refund or replacement via Egress Capital Partners Inc.
B Braun Medical recalled 2,840 NES1727KFX anesthesia tray kits distributed nationwide to healthcare facilities. The recall cites a potential mispositioned lid on the catheter connector. Healthcare providers should stop using the device immediately and follow recall instructions.
Enterix recalled 201,426 InSure ONE Fecal Immunochemical Test kits after a sensitivity failure linked to Test Card Lot TT241102. The issue may cause false negative results. Healthcare providers and patients should stop using the affected kits and follow the manufacturer’s recall instructions.
Percussionaire recalled 59,160 Phasitron 5 IPV In-Line Valve sets worldwide after an IFU update flagged a pressure-relief leak when used with ventilators. The defect endangers neonates and infants and patients under 10 kg with tidal volumes under 50 mL. Healthcare providers should halt use immediately.
FUJIFILM Healthcare Americas Corp recalled 16 CH-200 X-ray machines in the domestic market. The shaft that mounts the X-ray tube unit on the support may break. Protective parts may fail when the shaft breaks during frontward lifting. Healthcare providers should stop using the device immediately and follow recall instructions.
Private Label Skin Care Inc. recalled edunn clarity BP Treatment Cleanser 10% after benzene was detected. The recall covers lot numbers 58170A and 58172A with expiration September 2025. The product was distributed in California and Georgia.
Private Label Skin Care recalls Artisan of Skin Benzoyl Peroxide 10% cream after benzene detected. The product was distributed in California and Georgia. Consumers should stop use immediately and contact the company for guidance.
Skin MD by Dr Monika Kiripolsky recalled its Body Acne Cleanser after detecting elevated benzene levels. The recall covers products associated with Lot # 58170A and Lot # 58172A distributed in CA and GA. Consumers should stop use and seek guidance from a healthcare provider.
GE Medical Systems Israel recalls 11 Elscint Cardial dual-head gamma cameras used for cardiac imaging worldwide. The recall concerns detector mounting that could fail if the unit is moved without proper support. Hospitals should stop using these devices immediately and follow GE’s recall instructions.
Shanghai United Imaging Healthcare recalled 22 CT X-ray systems, including the uCT 550 MD, sold to healthcare facilities in the United States. A third-party outer cover can become trapped between the patient table and gantry, causing mechanical interference during table movement. Stop using the device and follow the manufacturer’s recall instructions immediately.
UIH Technologies recalls 3 units of Shanghai United Imaging Healthcare uMI 780 PET/CT systems after a third-party outer cover can trap between the patient table and gantry. The issue can obstruct table movement. Hospitals are urged to stop using the devices and follow recall instructions.
Epoca International recalls Paris Hilton mini beauty fridges sold before August 2024 due to a shorting electrical switch that can overheat and cause a fire. Consumers should stop using the recalled units and seek a full refund. Details and how to claim are on Epoca’s recall page or by phone.
Olympus Corporation of the Americas recalls its BF-P150 bronchoscope after updates to the instruction for use. The recall covers 1,019 units outside the U.S. Distribution was nationwide in the U.S. The agency classifies this as a high-hazard issue.
CareFusion 303 BD Alaris infusion pump modules and compatible infusion sets are recalled nationwide in the U.S. and multiple international markets. The recall covers reference numbers including C24101E and 10015414 and related SmartSite components. The defect may cause flow rate and bolus accuracy deviations, and incorrect occlusion timing. Stop using the device and follow recall instructions from
Olympus Corporation of the Americas recalls 361 units in the US and 258 units overseas as of September 11, 2025. The recall targets the EVIS EXERA b Bronchovideoscope BF-XT190. The update adds safety instructions for using bronchoscopes with laser, argon plasma coagulation, and high-frequency therapy equipment. Patients and healthcare providers should stop using the device immediately and follow a
Medline Recall: Excelsior Medical 0.9% Sodium Chloride Injection, USP, 10 mL fill prefilled saline flush syringes EMZ111240 is being recalled. The notice covers 8,267,150 syringes distributed across the United States and Canada. The risk is a concentration deviation of sodium chloride. Healthcare facilities should stop using the product and follow recall instructions. See the FDA recall page for完整
Harris Teeter recalls 295 units of Asiago Texas Toast distributed in eight states after discovering undeclared milk. The allergen milk was not listed in the ingredient statement. Consumers with milk allergies should avoid the product and seek refunds or replacements.