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Aesculap Inc. is recalling certain MINOP Trocar 150mm surgical instruments (model FF399R) because the shaft may be longer than intended. This surgical tool is used during minimally invasive procedures. No injuries have been reported so far.

Moderate·FDA·Mar 11, 2026·Aesculap

Siemens Healthcare Diagnostics recalled its Atellica CH Urine Albumin test kits because they may report falsely low results for high-protein urine samples. If a sample contains more than 40.0 mg/dL of albumin, the test may incorrectly show a value between 6.2 and 40.0 mg/dL instead. This affects all lot numbers of Material Number 11537225 distributed worldwide.

Moderate·FDA·Mar 11, 2026

B. Braun is recalling three models of 21-gauge winged infusion sets because the needle tip may be dull or blunt, difficult to advance, or break. The recall covers about 177,850 units distributed nationwide in the United States and in Costa Rica. No injuries have been reported.

Moderate·FDA·Mar 11, 20263 products

Staar Surgical EVO+ Visian Toric Implantable Collamer Lenses (Model VTICM5) were labeled as 12.1 mm but are actually 12.6 mm in length. The larger size can cause the lens to sit too high in the eye, potentially reducing eye drainage and increasing eye pressure, which may lead to discomfort, vision problems, or the need for lens removal.

Serious·FDA·Mar 11, 2026·Staar Surgical

Olympus is recalling three ShockPulse-SE lithotripsy system products, including the generator and reusable and single-use probes, with about 3,368 units affected. The generator can stay stuck in a blinking state and fail to recognize the transducer, which may be caused by damage to the transducer plug or generator receptacle. No injuries have been reported.

Moderate·FDA·Mar 11, 20263 products

Roche Diagnostics' cobas pro automated laboratory analyzer has a software defect that can cause it to accept incorrect calibrations. When this happens, the machine repeats the same result for multiple patient and quality-control tests instead of calculating new values, potentially leading to inaccurate lab results. This affects specific blood tests including ferritin, vancomycin, and light chain measurements.

Moderate·FDA·Mar 11, 2026·Roche Diagnostics

GE Healthcare has identified a software issue in certain versions of its Centricity Universal Viewer Zero Footprint Client where patient information displayed in the viewer may not match the medical images being shown. This could occur in specific workflows on systems with Patient Timeline installed. The issue affects approximately 250 units.

Serious·FDA·Mar 11, 2026

Abiomed is recalling three Impella RP heart pump models because the differential pressure (dP) sensor may malfunction and its readings may drift. The recall covers 4,966 units in total and was distributed in the US and several other countries. No injuries have been reported.

Serious·FDA·Mar 11, 20263 products

Mylan Pharmaceuticals is recalling specific lots of Amnesteem (isotretinoin) 40 mg capsules because they failed to meet dissolution specifications—meaning the medication may not break down and be absorbed by your body as intended. This could affect how well the medicine works. The recall affects two lots (3116110 and 3116130) with an expiration date of July 2026.

Moderate·FDA·Mar 11, 2026

New Life Pharma is recalling four sterile multi-dose vials of semaglutide and tirzepatide injection, all sold under the Nomida name, because the company cannot assure they are sterile. The recall covers 2 mg and 10 mg semaglutide vials and 10 mg and 15 mg tirzepatide vials, and the products were distributed in Ohio. No injuries have been reported.

Moderate·FDA·Mar 11, 2026·New Life Pharma4 products

Radnostix Sodium Iodide (I-131) Solution, a prescription oral therapeutic medication, is being recalled because some vials contain particulate matter due to production issues. The affected medication is in 1 ml, 2 ml, and 3 ml vials with batch number I012626R-01 and expiration date 02/09/2026. No injuries have been reported.

Moderate·FDA·Mar 11, 2026·Radnostix

Kirkman is recalling three topical numbing products, distributed by Dermal Source of Portland, OR: Five-Star Vasocaine spray, Maximum Zone 1 lidocaine cream, and Maximum Zone 2 lidocaine cream. The company's stability testing does not support the expiry dates printed on these products. No injuries have been reported.

Moderate·FDA·Mar 11, 2026·Kirkman3 products

Rising Pharmaceuticals is recalling specific bottles of Temozolomide 5mg capsules because testing found the medication didn't meet quality standards for purity and stability. The issue was discovered during routine 9-month stability testing. This affects 1,200 bottles distributed nationwide with expiration date 09/2026.

Moderate·FDA·Mar 11, 2026·Rising Pharma

Major Pharmaceuticals is recalling midodrine hydrochloride 5 mg tablets (Lot N02640, expiring 08/2027) because some blister packages are not properly sealed. Defective packaging could allow the medication to degrade or become contaminated. No injuries have been reported.

Moderate·FDA·Mar 11, 2026

Cipla USA is recalling specific lots of Nilotinib 150 mg capsules because testing found the capsules did not meet appearance and description standards after six months of storage. The affected lots are 5GJ0220, 5GJ0221, and 5GJ0222, with expiration date 04/30/2027. No injuries have been reported.

Moderate·FDA·Mar 11, 20262 products

Harbin Jixianglong Biotech distributed semaglutide (an injectable medication for compounding) without completing required manufacturing process and bacterial endotoxin testing. This means the drug may not meet safety and purity standards. The affected lot is CP-030-20250711 with an expiration date of July 24, 2027.

Moderate·FDA·Mar 11, 2026·Jixianglong2 products

Acme United Corporation is recalling 21 antiseptic and hand sanitizing towelette and wipe products nationwide for manufacturing (CGMP) deviations, a Class II classification. The products are sold under names including First Aid Only, Med-Nap, Dukal, Dynarex, Piedmont Sanitizing, Max Packaging, Savannah, Medi-First, Wipes Plus, WP WipesPlus, Green Guard, and Children's Healthcare of Atlanta, among others. No injuries have been reported.

Moderate·FDA·Mar 11, 2026·Acme21 products

Teva is recalling four strengths of metoprolol succinate extended-release tablets (25 mg, 50 mg, 100 mg and 200 mg), sold in 100- and 1,000-tablet bottles. The tablets did not meet the required dissolution specification, which means they may not release the medicine at the expected rate. No injuries have been reported.

Moderate·FDA·Mar 11, 20264 products

Remel's Campy CVA Medium (lot R01272, UDI 848838001055) is not reliably recovering Campylobacter Jejuni bacteria during laboratory culture testing. Customers reported low to no bacterial growth on this specific lot, which could lead to missed or delayed diagnoses.

Moderate·FDA·Mar 4, 2026

Medtronic found a manufacturing error in 2 units of the Octopus Nuvo Tissue Stabilizer where the tubing was installed backwards—the short tube was attached to the bottom and the long tube to the top, opposite of the correct design. This could affect how the device functions during use.

Moderate·FDA·Mar 4, 2026

Agiliti Health's Adapt Pump (used in Adapt Air and Adapt Convertible mattresses) has a software issue that prevents the temperature control (Microclimate Management) function from restarting after the Autofirm button is used for 10 minutes during initial setup. This only happens if you let the timer run out without manually stopping it, and it only affects temperature management—not the mattress's air support.

Moderate·FDA·Mar 4, 2026·Agiliti Health

Medline is recalling six kits that include Tego Connectors, including dialysis, central line, and dressing change kits from Medline and Centurion. Affected lots may have silicone seal doming or tearing, which can block fluid flow, delay or interrupt therapy, cause leakage, or allow air or biological contaminants into the body. No injuries have been reported.

Moderate·FDA·Mar 4, 20266 products

Edermy is recalling two PIE medical device products that did not have the required FDA 510(k) clearance. The recall covers 27 PIE Trolley System units and 11,202 PIE PAK units, sold nationwide in 18 states. No injuries have been reported.

Moderate·FDA·Mar 4, 2026·Edermy2 products

Encore Medical is recalling 3 implant products, 54 units in total, because the labeling on the knee and humeral socket implants is incorrect. The implants were distributed across the US in 17 states. No injuries have been reported.

Moderate·FDA·Mar 4, 2026·Encore Medical3 products

Olympus is recalling 20 urological and gynecological resection sheath and inner sheath models sold across the US. The company received complaints that the ceramic tip of the resection sheath can break. No injuries have been reported, and the agency has not specified a remedy.

Moderate·FDA·Mar 4, 202620 products

Olympus is recalling the Cystoscope Outer Sheath model WA22810A because it is incompatible with GreenLight Laser systems used for prostate (BPH) treatment. Using this sheath with the laser can damage the tip of the device, potentially affecting the safety and function of the cystoscope.

Moderate·FDA·Mar 4, 2026

MRIMed's SL-111 battery for the Mobile Exam Light (model SL-110) can overheat while charging, causing internal components to melt and create smoke. This affects 314 batteries with specific lot numbers distributed nationwide and internationally.

Moderate·FDA·Mar 4, 2026

Medline reported that the manufacturer of its sterile saline wound wash may not have made the products to the required sterility assurance level. The recall covers five products: a saline wound wash sold under the Medline and Meijer names, plus several Medline convenience kits. No injuries have been reported, and the products were distributed across the US and to the Bahamas, Bermuda, and the Cayman Islands.

Moderate·FDA·Mar 4, 20265 products

Hitachi is recalling two proton beam therapy systems because a software problem in the patient positioning system may cause the patient's position to be slightly off target. The recall covers two products, with one unit affected in each, distributed to Texas and Washington, D.C. No injuries have been reported.

Moderate·FDA·Mar 4, 2026·Hitachi2 products

Wizcure Pharma is recalling seven eye products sold nationwide: Vista dry eye drops (Vista Tears, Vista Gel, Vista Meibo Tears and Vista Gonio), Bio Glo and BioGlo fluorescein diagnostic test strips, and CHNaO fluorescein test strips. The FDA says the products were not made under current good manufacturing practices, so the company cannot assure they are sterile. No injuries have been reported.

Moderate·FDA·Mar 4, 2026·Wizcure Pharma7 products