Alaska recalls

IntegraDose Compounding Services LLC is recalling Vasopressin 2 Units/2 mL syringes because the drug may contain less active ingredient than labeled. This affects two specific lots distributed nationwide. No injuries have been reported.

VistaPharm's Kerr Insta-Char activated charcoal product did not meet the required Over-the-Counter (OTC) Monograph standards set by the FDA. The affected product is a 240 mL bottle containing 50 grams of activated charcoal in a sorbitol base with cherry flavor (Lot #AH001, expiring 8/31/2026).

VistaPharm's Kerr Insta-Char activated charcoal suspension did not meet the standards required for over-the-counter products. The product was distributed nationwide, and affected lots should not be used.

VistaPharm's Kerr Insta-Char activated charcoal product did not meet the required OTC Monograph M023 standards set by the FDA. The affected product is a 240 ml bottle containing 50 grams of activated charcoal with cherry flavor (Lot #AE001, expiring 5/31/2026) distributed nationwide.

VistaPharm's Kerr Insta-Char activated charcoal product failed to meet required Over-the-Counter (OTC) monograph standards. The product may not perform as intended or meet quality requirements for safety and effectiveness.

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.

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.

CooCooBaby Classic and Deluxe Baby Loungers have design flaws that create unsafe sleeping conditions for infants. The sides are too short to keep a baby secure, the sleeping pad is too thick and can cause suffocation, and babies can fall out or get trapped at the foot opening.

Joolz Aer2 Car Seat Adapters can fail to attach properly to Joolz Aer2 strollers, allowing the car seat to fall. The company has received one report of the adapters detaching. No injuries have been reported so far.

SHEIN Distribution Corporation is recalling Michley-branded children's pajamas sold online because they don't meet mandatory flammability standards for sleepwear. The recalled one-piece pajamas came in green, pink, yellow, and purple with animal patches, in sizes 80–130. They pose a risk of serious burn injuries.

Arizer Solo III portable vaporizers with certain serial numbers contain a defective lithium-ion battery that can overheat, explode, or ignite, posing a serious fire and burn risk. The company has received four reports of batteries exploding or catching fire. About 5,000 units sold between May 2025 and January 2026 are affected.

Veseacky children's pajama sets sold on Amazon do not meet mandatory federal safety standards for sleepwear and pose a risk of serious burns to children. The sets consist of a long-sleeve button-up top and matching pants, sold in various colors and prints from October 2020 through January 2026.

Arrogantf white spa and hot tub drain covers do not meet federal safety standards for entrapment protection. They pose a risk of serious injury or death from entrapment and drowning, particularly to children. About 340 units were sold online through Amazon between September 2025 and March 2026.

GOPO Toys pull string teething toys have silicone strings that are longer and thinner than safety standards allow. The strings can reach the back of a child's throat and become lodged, causing choking or respiratory distress. The company has received three reports of strings reaching children's throats.

BABESIDE toy sets sold on Amazon contain small parts that pose a choking risk to children under 3: a pacifier and a plush bear with detachable eyes. These pieces are not safe for young children and violate federal small parts rules.

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.

AVID Medical, Inc. distributed 60 kits of Halyard Eye Bag Pack (Kit Code UIEB48-01) with sealed pouches that did not undergo validated sterilization. The affected kits were distributed nationwide in Iowa. No injuries have been reported.

Halyard Drape Pack kits (Code LMDP36-01) were distributed without proper sterilization validation. Approximately 72 kits shipped with sealed pouches that had not undergone the required sterilization process. These kits were distributed nationwide and in Iowa.

AVID Medical inadvertently distributed 224 kits of Halyard Towel Six Pack (Kit Code AMTS70-01) with sealed pouches that had not undergone validated sterilization. The affected kits were distributed nationwide, with concentration in Iowa. No injuries have been reported.

AVID Medical distributed 120 sealed Halyard Pain Pack kits (Kit Code AMPK48-01, Lot 334669) that did not undergo proper sterilization validation. The affected kits were distributed nationwide, with known distribution in Iowa. No injuries have been reported.

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.

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.

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.

Boston Scientific has recalled certain reusable TCN Electrodes used in neuromodulation devices because they may not perform as expected. The affected electrodes come in multiple sizes and configurations, with about 49,251 units distributed worldwide.

Boston Scientific has recalled certain CSK Electrode models used in neuromodulation procedures because they may not perform reliably as intended. The affected electrodes come in multiple configurations and lengths. No injuries have been reported to date.

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.

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.

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.

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.

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.