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Medtronic has recalled certain MiniMed 780G insulin pumps due to software defects that can cause the pump to deliver too much insulin, too little insulin, or stop delivering insulin entirely. These defects appeared after software updates (versions 6.60, 6.61, and 6.62) and may result in dangerously high or low blood sugar levels. The recall affects over 26,000 pumps with specific serial numbers.

Serious·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

Philips is recalling 11 ultrasound transducer models to clarify and update labeling that defines how long these devices are expected to remain in use. The recall was filed for clarification, and no injuries have been reported.

FDA·Apr 1, 202611 products

Philips is recalling four Trilogy ventilator models running software version 1.05.15.00: Trilogy Evo, Trilogy Evo O2, Trilogy EV300, and Trilogy Evo Universal. When non-pneumatic nebulizers are used with these ventilators, the breath volume the patient receives may differ from the amount the device is set to deliver. No injuries have been reported. The recall covers about 113,717 units per model and was distributed nationwide and in many other countries.

Serious·FDA·Apr 1, 20264 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

The Handy Solutions Neck & Shoulders Heating Pad (model 25607) can overheat and cause burns if folded while in use or placed under your body. When folded, the device's safety temperature sensor cannot detect the excessive heat, so it does not shut off. The pad may emit a burning smell before melting or catching fire.

Serious·FDA·Apr 1, 2026

Merit Medical is recalling five products, including CentrosFLO and DuraMax dialysis catheters and 16F dual valved splittable sheath introducers. The sheath introducer may not split as intended, which can cause bleeding, pieces left in the body, procedure delays, or blood clots. No injuries have been reported.

Serious·FDA·Apr 1, 20265 products

Erbe is recalling three models of flexible cryoprobes used in surgery because the probes may rupture or burst during activation. The recall covers about 40,900 units sold nationwide, including Puerto Rico. No injuries have been reported.

Serious·FDA·Apr 1, 2026·Erbe3 products

SiluetaYa Mexican Tejocote Roots Supplement Pieces contain yellow oleander, a toxic plant that can cause serious illness. The affected product was sold online in Arizona, California, New Mexico, New York, Texas, and Utah. This is a Class I recall, the FDA's most serious category.

Serious·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

Macleods Pharma USA is recalling Levothyroxine Sodium Tablets USP 150 mcg because they may contain less active ingredient than labeled. This means the medication may not work as intended to treat thyroid conditions. The affected lot is 16240062A with an expiration date of March 2026.

Moderate·FDA·Apr 1, 2026

Chiesi USA is recalling specific lots of CUROSURF, a medication given to premature infants to help them breathe. The company cannot confirm that all vials are sterile, which means they may be contaminated. No infections have been reported so far.

Moderate·FDA·Apr 1, 2026

Radnostix Gelatin Capsule Packs used with Sodium Iodide I-131 Kit have failed quality specifications. The affected capsules may not perform as intended. Three specific lots distributed nationwide are involved.

Moderate·FDA·Apr 1, 2026·Radnostix

Datascope's Battery Charging Station (Model 0998-00-0802) for Cardiosave IABP batteries has a protruding screw in the left bay that can prevent certain batteries from inserting fully and charging properly. The right bay works normally. This affects 28 units distributed in select U.S. states and international locations.

FDA·Mar 25, 2026

Hologic's Aptima HPV Assay test kits (Master Lot 929785) may produce invalid results or false negatives, meaning they could fail to detect HPV infection. The affected kits were distributed to healthcare facilities in California, Florida, Iowa, Illinois, Missouri, North Carolina, New Mexico, Puerto Rico, and Tennessee.

Moderate·FDA·Mar 25, 2026

Diagnostica Stago's STA Liatest D-Di blood test kits are giving inaccurate measurements for D-dimer (a marker used to help rule out blood clots). The kits are showing higher-than-actual results across all test ranges. These kits are used in hospital and reference laboratories on specific analyzer machines.

Moderate·FDA·Mar 25, 2026

ConvaTec's EsteemBody Drainable Pouch (model REF:423643, 10–45mm) may leak because of a manufacturing issue. The affected pouches have lot numbers 5K00011 or 5K00714 and have been distributed worldwide. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·ConvaTec3 products

LeMaitre Vascular is recalling one unit of Artegraft Vascular Graft (Model AG740) distributed in Illinois due to a labeling mix-up on the outer packaging. The product box was labeled with an incorrect lot number, which could cause confusion during clinical use. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·LeMaitre Vascular

The Welch Allyn Spot Vision Screener VS100 (software version 3.2.0.1) may display an unintended flickering screen due to a software issue. Flickering lights can trigger seizures in people who are photosensitive.

Moderate·FDA·Mar 25, 2026

The external screws that secure the cover on the Howmedica Osteonics MICS3 Angled Sagittal Saw Attachment may loosen during use and detach. This affects all units with part number 210490 distributed across the United States and several other countries. No injuries have been reported.

Moderate·FDA·Mar 25, 2026

GE is recalling three versions of Centricity Universal Viewer software, a program that displays medical images, including mammograms. User login credentials may be exposed on the local workstation, which could let an unauthorized person affect system availability or manipulate data. The recall covers 2,405 affected units, and no injuries have been reported.

Moderate·FDA·Mar 25, 20263 products

Abbott Diagnostics has recalled certain lots of the ID NOW Influenza A & B 2 test kit because they produce an unusually high number of invalid results compared to what the instructions say to expect. Invalid results mean the test does not give a clear positive or negative answer, requiring a retest.

Moderate·FDA·Mar 25, 2026

Winder Laboratories is recalling certain batches of their grape-flavored multivitamin with fluoride chewable tablets because they contain less vitamin D than stated on the label. The FDA discovered this during an inspection. The affected products are the 0.25 mg and 1 mg formulations with specific lot numbers and expiration dates in October and November 2025.

Moderate·FDA·Mar 25, 2026·Winder Laboratories