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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, 20264 products

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, 20262 products

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

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

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, 20262 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

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

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

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, 202622 products

BD Kiestra ReadA lab automation systems (Catalog No. 446948) may occasionally lose remote connectivity after a system reboot, which could temporarily delay plate retrieval from the incubator. The issue is intermittent and does not affect test results, assay performance, or sample integrity. This affects 82 units distributed across the United States and internationally.

Moderate·FDA·Apr 8, 2026·BD Kiestra

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

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

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

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

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, 20268 products

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

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

The labeling on BD Alaris System with Guardrails Suite MX does not specify which version of Transport Layer Security (TLS) must be enabled on hospital networks for secure Wi-Fi communication with Point-of-Care Units. This could create confusion during setup and potentially leave devices with inadequate security settings.

Moderate·FDA·Apr 1, 2026

Olympus is recalling seven models of bipolar and PK/PKS cutting forceps, 3,788 units in total, used in medical procedures. The supplier did not adequately validate a welding process for components, and defective welds could cause the forceps' jaw to break during clinical use. No injuries have been reported.

Moderate·FDA·Apr 1, 20267 products

Tandem Diabetes Care insulin pumps distributed in the Czech Republic and Slovakia have translation errors in their Czech language user guide. The most serious error tells users to verify the infusion set is connected to the body when it should say the opposite—that it should NOT be connected. Following these incorrect instructions could cause unintended insulin delivery and dangerously low blood sugar.

Moderate·FDA·Apr 1, 2026

AMO has recalled certain TECNIS Eyhance intraocular lenses (IOLs) used in cataract surgery because a small number may have a defect where the lens haptic (support arm) sticks to the optic, preventing proper unfolding during implantation. This affects 361 lenses distributed across 12 U.S. states. No injuries have been reported.

Moderate·FDA·Apr 1, 2026·AMO

Straumann is recalling two custom abutment products, 20 units in total, for dental implant use. A raw material bar of TAN material was mislabeled as titanium Grade 4, so some RC Titanium abutments were made from the wrong material. The affected units were distributed in several U.S. states and in Canada. No injuries have been reported.

Moderate·FDA·Apr 1, 20262 products

Koven Technology's BiDop 3 Pocket Doppler ultrasound device was distributed with labeling that claims it can be used for fetal applications, but the FDA never approved it for that use. The device is only cleared to detect blood flow in blood vessels, not for fetal monitoring. Using it for unapproved purposes could lead to incorrect results or missed diagnoses.

Moderate·FDA·Apr 1, 2026·Koven Technology

Orthalign drill plates (Trimax-Pegged, Sizes 1–5, REF 402566) in one lot may have been made outside specifications. This could cause bone cuts larger than intended during knee surgery. Seven units were distributed in Utah.

Moderate·FDA·Apr 1, 2026·Orthalign2 products

Olympus is recalling four endoscope products because the MAJ-1443 and MAJ-1444 valves are no longer compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. The recall covers about 139,000 units across the US, and no injuries have been reported.

Moderate·FDA·Apr 1, 20264 products

Beckman Coulter has recalled MicroScan Neg MIC 56 antimicrobial susceptibility testing panels (Catalog C42464, Lot 2026-01-03) due to potential contamination in the test wells. These panels are used by laboratories to identify bacteria and test antibiotic resistance. Contaminated panels could produce inaccurate test results.

Moderate·FDA·Apr 1, 2026

I.T.S. is recalling 17 orthopedic implant product lines, including bone plates and screw systems. Updated MRI safety testing found that these implants can heat up more during certain MRI conditions than the product instructions previously stated. No injuries have been reported.

Moderate·FDA·Apr 1, 2026·I.T.S17 products

GE Medical Systems' Imactis CT-Navigation System (Models E85101LA and E85101LP) has a potential issue where the needle's simulated path shown to the doctor may not match where the needle actually goes during CT-guided procedures. This discrepancy could affect the accuracy of needle placement during medical procedures. No injuries have been reported.

Moderate·FDA·Apr 1, 2026

American Health Packaging is recalling specific batches of Meclizine Hydrochloride 12.5 mg tablets because they failed to meet required tablet specifications. The affected product is Lot #1024852 with an expiration date of 9/30/2026. No injuries have been reported.

Moderate·FDA·Apr 1, 2026

Teva Pharmaceuticals is recalling specific lots of Octreotide Acetate injectable suspension due to sterility concerns identified at the manufacturing facility. The FDA found quality system deficiencies that could affect the safety of the medication.

Moderate·FDA·Apr 1, 20263 products