Hawaii recalls

Sold nationwide. Medline is recalling 7 kit products that contain Olympus single-use biopsy valves, totaling about 14,379 kits. Olympus found more complaints of rubber fragments detaching from a slit in the valves. A loose fragment could lodge in a patient's airway and may need to be removed in a procedure. No injuries have been reported.

Serious·FDA·Apr 8, 2026·Medline7 products

Sold nationwide. Summa Therapeutics is recalling certain Finesse BTK Multicath injectable angioplasty balloon catheters because the balloon may not meet burst strength specifications. This could cause the balloon to rupture unexpectedly during a medical procedure. The recall affects 22 units distributed in New Jersey and Florida.

Moderate·FDA·Apr 8, 2026·Summa Therapeutics

Sold nationwide. Synthes is recalling two bone screw taps, the VOLT Locking Screw Tap and the VOLT Cortex Screw Tap, because two production lots were swapped, so the taps may have an incorrect thread. The recall covers 110 units across 21 states, and no injuries have been reported.

Moderate·FDA·Apr 8, 2026·Synthes2 products

Sold nationwide. Intuitive Surgical is recalling two da Vinci S and Si reusable surgical instruments, totaling 8,247 units, after the company received complaints of frayed or broken pitch cables. The products were distributed across the U.S. and in many other countries. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·Intuitive Surgical2 products

Sold nationwide. Intuitive Surgical is recalling four reusable instrument models used with da Vinci S and Si robotic surgical systems. The company received increased complaints of broken or frayed grip cables. No injuries have been reported, and the instruments were distributed in the U.S. and in many other countries.

Moderate·FDA·Apr 8, 2026·Intuitive Surgical4 products

Sold nationwide. Olympus is recalling some SOLTIVE laser systems because a 24V power supply module may fail and make the system inoperable. The defect may also cause smoke or a burning smell, which is designed to stay inside the laser console and extinguish itself. No injuries have been reported. The recall covers 2 products, with 440 units affected, distributed in the US and several other countries.

Moderate·FDA·Apr 8, 2026·Olympus2 products

Sold nationwide. Medline Industries identified a potential breach in the sterile pouch packaging of one lot of Sterile Radiology Procedure Kits (Model DYNDH1491B). This breach may allow the kit to lose its sterile condition. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·Medline

Sold nationwide. Philips Vue Motion V12 cardiac imaging software (Product Number 1017979, software versions 12.2.0 through 12.2.8.500) may display image frames out of sequence during dynamic cine runs. This could cause medical staff to review cardiac images in the wrong order, potentially affecting diagnosis.

Moderate·FDA·Apr 8, 2026·Philips

Sold nationwide. Medline recalled two products: ENFit G-tube connectors and kits that contain them. The connectors were not made to required dimensions, so they may not seal properly with ENFit-style devices and can leak. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·Medline2 products

Ultradent Products is recalling Jiffy Original Composite Polisher Cups (Coarse) 12pk because the cups may crumble or break apart during use. This could delay dental treatment. The affected product has lot number 529983 and expiration date of September 2, 2031.

Moderate·FDA·Apr 8, 2026·Ultradent Products

Sold nationwide. The surgical light assembly in Stryker CHROMOPHARE Softlit Ring systems may not adequately support the weight of the ceiling cover. This could potentially cause the cover to fall. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·Stryker

Sold nationwide. Mentor is recalling 7 product lines of breast tissue expanders, including CPX 4 US and Artoura models. The recall notice says the needle tip may be dull or blunt, which could make it hard to advance or cause it to break. No injuries have been reported. The notice refers to infusion sets, while the listed products are tissue expanders, so check the notice for details.

Moderate·FDA·Apr 8, 2026·Mentor7 products

Sold nationwide. Philips is recalling 22 models of its Allura Xper and Azurion X-ray imaging systems. The recall covers a wired foot switch that may fail to start X-ray imaging or may start it intermittently. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·Philips22 products

Sold nationwide. Siemens has recalled certain lots of its Atellica CH A1c_E hemoglobin test kit because when used with another reagent (RCRP) on the same analyzer, the A1c test may give lower-than-accurate results. Lower results could delay diabetes diagnosis or lead to inadequate treatment. This issue does not affect labs using separate analyzers for each test.

Moderate·FDA·Apr 8, 2026·Siemens

Sold nationwide. ReCor Medical distributed one Paradise ultrasound renal denervation catheter (Model PRDS-068-02, Lot M4907) that did not meet manufacturing standards and was supposed to be destroyed. The device was distributed in nine U.S. states. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·ReCor Medical2 products

Sold nationwide. Philips is recalling four Trilogy ventilator models running Software Version 1.05.15.00, covering 113,717 units in total. In some situations, the Obstruction Alarm does not sound within the time required by applicable standards and may take up to four breaths to trigger. No injuries have been reported.

Serious·FDA·Apr 8, 2026·Philips4 products

Sold nationwide. Abiomed's Impella Controller may display a delayed "Purge System Blocked" alarm when used with first-generation Impella 5.5 pumps. This could prevent timely detection of a blocked purge system. The issue affects 62 controllers with specific serial numbers in software versions 8.2.2 through 8.5.

Serious·FDA·Apr 8, 2026·Abiomed

Sold nationwide. Abiomed is recalling purge cassettes used in Impella heart pump systems because Generation 1 cassettes have an increased risk of leaking during use. This affects multiple Impella pump models sold globally, with specific batch numbers identified from 2024.

Serious·FDA·Apr 8, 2026·Abiomed

Imu-Tek Animal Health is recalling two products: Imu-Tek Colostrum-5 120-capsule bottles and Imu-Tek Colostrum-5 powder bottles. The company says the product may not have been fully processed. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·Imu-Tek2 products

Sold nationwide. Lone Star Dairy Products LLC is recalling spray dried milk powder products because Salmonella bacteria was found during testing of finished products. The recall affects specific lot codes of NFDM Low Heat, NFDM High Heat, and SMP Medium Heat products sold in 25 kg bags and 1 metric ton totes.

Serious·FDA·Apr 8, 2026·Lone Star Dairy Products

Sold nationwide. Some cartons of Amneal Magnesium Sulfate IV bags were mislabeled and contained Tranexamic Acid (a different medication) instead. This mix-up affects lot AH250162 with an expiration date of 8/31/2027. The error was discovered before the product reached patients.

Serious·FDA·Apr 8, 2026·Amneal Pharmaceuticals

Sold nationwide. Appco Pharma LLC is recalling prazosin hydrochloride 1mg capsules (100-count bottles) because they may contain higher-than-acceptable levels of a nitrosamine impurity. This impurity was detected during manufacturing quality checks. The recall affects specific lot numbers distributed nationwide.

Moderate·FDA·Apr 8, 2026·Appco Pharma3 products

Sold nationwide. K.C. Pharmaceuticals is recalling eight sterile eye drop products because the company cannot confirm they are sterile. The drops were sold under store and pharmacy brands including Best Choice, Walgreens, GERI CARE, LEADER, Good Sense, Industrial Eye Relief and Rugby. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·K.C. Pharmaceuticals8 products

Sold nationwide. Amneal Pharmaceuticals is recalling specific lots of tramadol 50 mg tablets because they contain higher-than-allowed levels of a chemical impurity called N-nitroso-desmethyl-tramadol (NDSRI). The impurity was discovered during stability testing of tablets nearing the end of their shelf life. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·Amneal Pharmaceuticals

Sold nationwide. Alembic Pharmaceuticals is recalling specific lots of Bromfenac Ophthalmic Solution 0.07% because the medication failed purity and degradation tests during stability testing at 20 months. The affected eye drops may contain higher-than-acceptable impurity levels, which could affect safety and effectiveness.

Moderate·FDA·Apr 8, 2026·Alembic Pharmaceuticals

Sold nationwide. Liquid Blenz Corp. is recalling all Good Brain Tonic beverages (16 oz and 32 oz bottles) due to a potential botulism risk. Botulism is a serious form of food poisoning. No illnesses have been reported yet, but the product was distributed nationwide.

Serious·FDA·Apr 6, 2026·Liquid Blenz

Sold nationwide. Raw Farm has recalled specific batches of raw cheddar cheese products (blocks and shredded) due to a potential link to an E. coli O157:H7 outbreak. The recall includes multiple batch numbers and expiration dates listed on the Raw Farm website. No pathogens have been found in Raw Farm products tested so far.

Serious·FDA·Apr 2, 2026

Sold nationwide. The canopy beams on certain Samson International bed frames can collapse, especially when the bed is moved. The company has received five reports of the canopy collapsing and striking people, resulting in shoulder and head injuries.

Serious·CPSC·Apr 2, 2026·Samson

Sold nationwide. Tuymec Minoxidil Hair Growth Spray bottles sold on Amazon do not have child-resistant caps, violating federal safety rules. Minoxidil is toxic if swallowed by young children and can cause serious injury or death.

Serious·CPSC·Apr 2, 2026·DrHealBeauty

Sold nationwide. Sam's Club is recalling Member's Mark Valentine-themed children's pajama sets because they don't meet mandatory flammability standards for sleepwear. This poses a risk of burn injuries. About 18,000 sets were sold online between December 2025 and January 2026.

Serious·CPSC·Apr 2, 2026·Hansoll Textile