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VistaPharm is recalling four sizes of Kerr Insta-Char activated charcoal with cherry flavor, in aqueous and sorbitol bases. The product did not meet the FDA over-the-counter monograph M023 standard. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·Pain Train Salsa4 products

Glenmark Pharmaceuticals is recalling specific lots of Alyacen 7/7/7 (a birth control pill) because testing found higher-than-allowed impurity levels in the tablets. The affected lots were distributed nationwide. No injuries have been reported.

Moderate·FDA·Jun 24, 2026

Ricon S-Series and K-Series wheelchair platform lifts may have a faulty electrical contactor that prevents the controls from stopping the lift. This means a lift could continue moving while someone is on it, creating an injury risk.

Moderate·NHTSA·Jun 23, 2026·Ricon Corporation

Certain Rockford Fosgate amplifier models (20GLADR-STG5, 24WRNGLR-FOX, 24WRNGLER-STG3, and 18WRNGLER-STG5) contain a 150-amp fuse that may not protect the circuit properly if a short circuit occurs. This inadequate protection could increase the risk of fire.

Moderate·NHTSA·Jun 23, 2026·Rockford Corporation

MorningStar Farms is recalling two products because they may contain plastic pieces. The affected items are Buffalo Chik'n Nuggets (10.5 oz) and Hot & Spicy Sausage Patties (8 oz) with specific "Better if Used Before" dates in early July 2027.

Moderate·FDA·Jun 18, 2026·Morningstar Farms

Power Plate Meals frozen meatloaf with garlic mashed potatoes contains soy, a known allergen, that is not listed on the package label. The affected products were produced between June 25, 2025, and June 10, 2026, and were sold in Minnesota, North Dakota, and South Dakota. No injuries have been reported.

Moderate·USDA·Jun 18, 2026

Boston Scientific is removing Orca Sterile Single Use Air/Water and Suction Valves from distribution because the suction button is sticking more often than expected. These valves are used during gastrointestinal endoscopic procedures to control air and water flow on endoscopes. No injuries have been reported.

Moderate·FDA·Jun 17, 2026

AVID Medical is recalling four Halyard kit types because sealed pouches were distributed without validated sterilization. The kits may not be sterile, and the recall includes 476 kits total, distributed in Iowa. No injuries have been reported.

Moderate·FDA·Jun 17, 20264 products

Elekta's MOSAIQ Oncology Information System software (version 3.2) may fail to load an adapted baseline shift plan during cancer treatment delivery if a communication error occurs. This could affect the accuracy of radiation therapy positioning. No injuries have been reported.

Moderate·FDA·Jun 17, 2026

Abbott's Merlin PCS 3650 programmer software (versions 25.0.1 through 28.7.1) may malfunction during pacing capture threshold tests on pacemakers. When this occurs, the programmer may fail to successfully send the command to stop the test.

Moderate·FDA·Jun 17, 2026

Boston Scientific is recalling the Model SC-4318 Clik X Anchor (Lot #35107836) because sterile anchors may lack proper sterility assurance. Approximately 43 units were distributed across six U.S. states.

Moderate·FDA·Jun 17, 2026

Boston Scientific is recalling two lines of reusable electrodes, CSK and TCN, because they may not meet expected performance levels. The recall covers 2 products with about 81,000 units total, distributed across the US and several other countries. No injuries have been reported.

Moderate·FDA·Jun 17, 20262 products

Fresenius Medical Care's Bicarby Dialysate (Model RFP-400-G) has incorrect barcode labeling on some units. While the case label and printed information are correct, scanning the GTIN barcode alone could lead to identification errors. This could result in use of a dialysate with a potassium concentration different from what was prescribed.

Moderate·FDA·Jun 17, 2026

Some units of Inter-Med's Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit (catalog 504600-28) contain the package insert for Ferric Sulfate Gel instead. The wrong insert gives incorrect first aid instructions—specifically, it tells users to induce vomiting if the gel is swallowed, when the correct instructions say not to induce vomiting.

Moderate·FDA·Jun 17, 2026·Inter-Med

DT MedTech discovered that some Hintermann Series Talar Implant units labeled as left implants actually contained right implants inside the packaging. This mix-up was found through customer complaints. A total of 67 units across five US states and two countries are affected.

Moderate·FDA·Jun 17, 2026·DT MedTech

Three lots of Siemens Dimension Tacrolimus Flex Reagent Cartridges show a potential positive bias in quality control and patient test results. This means the cartridges may report tacrolimus levels that are higher than actual values. The affected lots are FA6254, FA6260, and FA6286.

Moderate·FDA·Jun 17, 2026

The EXENT Analyser, an automated blood-test device, has a software issue where certain test plates were marked as passed without performing required quality checks. This could allow inaccurate M-protein measurements—either missed detections or wrong concentration values—to be reported to clinicians.

Moderate·FDA·Jun 17, 2026·The Binding Site

Medartis has recalled certain APTUS 5.0 headed cannulated compression screws (CCS) used in bone fixation surgery because the central hole in the screw is not properly centered. This affects 13 units across five states. No injuries have been reported.

Moderate·FDA·Jun 17, 2026·Medartis

Sagemax Bioceramics is recalling NexxZr T Multi A3.5 W98-16mm zirconium oxide discs used in dental crowns and bridges. Some discs may have a reduced or missing dentin layer, which can weaken them and cause fractures when patients chew or bite.

Moderate·FDA·Jun 17, 2026·Sagemax

In2bones USA has recalled NeoSpan SuperElastic Compression Staples used in hand and foot surgery because the required Magnetic Resonance Imaging (MRI) safety symbol is missing from the product packaging, inner trays, and patient labels. This labeling omission could prevent patients and healthcare providers from knowing whether the implant is safe to use during an MRI scan.

Moderate·FDA·Jun 17, 2026·In2bones

One Philips DigitalDiagnost C90 Flex/Value/Chest/ER X-ray system was shipped without the required Seismic kit for its Wall Stand VS2. The kit is designed to keep the stand stable and prevent damage during earthquakes or seismic events.

Moderate·FDA·Jun 17, 2026

When using two or four amplifiers together in certain configurations, the SD LTM 64 PLUS may display a 1-second timing delay between channel blocks. This delay could cause doctors to misinterpret EEG test results. The issue affects devices running specific firmware versions.

Moderate·FDA·Jun 17, 2026·Micromed

Avanos Medical is recalling 20 PEG feeding tube kits sold under the CORFLO and MIC Safety names. The kits were made with lidocaine hydrochloride injection that is itself subject to a supplier recall for quality issues. No injuries have been reported.

Moderate·FDA·Jun 17, 2026·Avanos Medical20 products

HF Acquisition Co LLC is recalling the SporeTraq Mail-In Spore Testing Service (52 tests) because some test strips were not incubated for the correct length of time. The test strips are used by healthcare facilities to verify that their sterilization equipment is working properly. Incorrect incubation times can produce unreliable test results.

Moderate·FDA·Jun 17, 2026·HF Acquisition2 products

InspireMD is recalling six sizes of its CGuard Prime Carotid Stent System, covering 1,377 units in total. The stent delivery system may run into complications during deployment, which can cause high resistance or prevent the stent from being deployed. No injuries have been reported.

Moderate·FDA·Jun 17, 2026·InspireMD6 products

D.O.R.C. has recalled certain TDC VELOCE 23G Two Dimensional Cutters used in ophthalmic surgery because the outer knife can become loose during use. An increased number of complaints about this issue prompted the recall. No injuries have been reported.

Moderate·FDA·Jun 17, 2026·D.O.R.C3 products

Fresenius Medical Care is notifying users of potential leaks in Bicarby Dialysate products during setup and use. Fluid leaks from the luer-lock connection can create a slip and fall hazard on the floor where treatment is taking place.

Moderate·FDA·Jun 17, 2026

Some Berlin Heart EXCOR Pediatric Ventricular Assist Device blood pumps have mismatched expiration dates between the inner and outer package labels. The inner package shows an incorrect expiration date, which could cause confusion and delay surgical procedures if the device is not used on time.

Moderate·FDA·Jun 17, 2026·Berlin Heart

Certain lots of Mozarc Medical's Mahurkar Elite PASS Trays are missing the Tegaderm CHG antimicrobial dressing that is supposed to be included in the kit. These trays are used in hospitals and clinical settings for acute hemodialysis, aphaeresis, and infusion procedures. The missing dressing may affect the product's intended sterile barrier protection.

Moderate·FDA·Jun 17, 2026·Mozarc Medical

GE HealthCare found a possible problem with an electrical cable in certain Allia IGS X-ray systems that use Gaia generators. The issue could expose service personnel to electrical shock while working inside the C-FRT cabinet with power on. This recall includes 5 product lines, with 173 affected units in total.

Moderate·FDA·Jun 17, 20265 products