Massachusetts recalls

Metal springs in the detachable hinged lids of Kitchen HQ brand thermal insulated bowls can catch fire when used in the microwave. HSN has received 30 reports of the bowls smoking, sparking, melting, or catching fire, including one that caused property damage.

Joyin's Sloosh dive sticks (model 40041) are too hard and can cause serious piercing injuries if children fall or land on them in shallow water. Facial and eye injuries are also possible when retrieving sticks underwater. These sticks violate federal safety standards for dive toys.

BD is recalling specific lots of ChloraPrep Clear 1 mL and FREPP Clear 1.5 mL skin preparation applicators due to potential fungal contamination (Aspergillus penicillioides) that could grow under certain environmental conditions. The affected products were distributed to hospitals and medical distributors between March and June 2024.

Target is recalling Up & Up Fragrance Free and Fresh Cucumber Scented Baby Wipes after FDA testing found harmful bacteria (Burkholderia cepacia complex and Burkholderia gladioli) in product samples. Some customers also reported discoloration. These bacteria can cause serious infections, especially in newborns and infants with developing immune systems.

Ballester Hermanos is recalling limited packages of Pearl Milling Company Original Pancake & Waffles Complete mix (5.99 oz) sold in Puerto Rico. The label incorrectly stated "may contain" milk and soy instead of "contains" these allergens, creating a serious risk for people with allergies to these ingredients. No illnesses have been reported so far.

Pearl Milling Company Original Pancake & Waffles mix (5.99 oz pouches) sold in Puerto Rico contains milk and soy but was labeled as "may contain" instead of "contains." People with milk or soy allergies could have a serious allergic reaction if they consume it.

The fan blade in Vornado SRTH tower heaters can detach from the motor shaft, causing the fan to slow or stop. This leads to overheating and melting of internal parts, which can ignite and cause a fire if the safety cutoff fails. Vornado has received 32 reports of overheating, including 8 fires and 1 smoke inhalation.

The SUNS SS6291 interlock switch, used in residential elevators, can get stuck in a retracted position. When this happens, the exterior elevator door may stay unlocked even when the elevator moves to another floor, creating a risk of falling or being crushed.

The hard plastic outer shell on these bottles can bubble or peel, creating loose pieces of film-like plastic that a baby could choke on. The manufacturer has received 135 reports of this issue, though no injuries have been reported yet.

Broqixin-branded pool drain covers do not meet federal safety standards and can trap swimmers underwater, creating a drowning hazard. The white plastic covers (Model 11064W, about 7.36 inches wide) were sold online through Amazon from January to April 2026.

Gudook-branded bicycle helmets (model KY-055) do not meet mandatory safety standards for impact protection. The helmets can fail to protect your head in a crash, creating a serious injury or death risk. Only helmets with batch number 202503 and manufacture date March 2025 are affected.

Crenlux pool drain covers do not meet federal safety standards and can trap swimmers or bathers underwater, creating a serious drowning hazard. The white plastic covers, about 8 inches in diameter, were sold online through Amazon from June 2025 to March 2026.

Tiny Land children's play tents contain fiberglass poles that can shed fibers, causing skin and eye irritation. The company has received eight reports of fiber shedding resulting in irritation. The tents were sold online from November 2025 through March 2026.

Little Grape Land nursing pillows sold on Amazon do not meet federal safety standards and can obstruct an infant's breathing. The U-shaped pillows, sold in various patterns between August 2025 and April 2026, pose a serious risk of suffocation during infant feeding or tummy time.

Wyze Solar Cam Pan security cameras can overheat and catch fire if installed incorrectly. The incorrect assembly instructions may lead users to accidentally puncture the lithium-ion battery's metal casing with a long, flat-head screw, causing the battery to rapidly overheat. The company has received reports of six cameras catching fire and exploding, with six consumers suffering minor burns.

Some Medline EYE TRAY-LF convenience kits (SKU DYNJ21627P) contain syringes labeled as tuberculin syringes on the box, but the actual syringes inside are insulin syringes. Using the wrong syringe type could lead to incorrect dosing.

Hard drives in Philips Allura X-ray imaging systems may degrade after six years of use, potentially causing loss of imaging capability, motorized movement, or data. Some systems may temporarily restore function after a restart.

Hard drives in Philips Azurion imaging systems may degrade after six years of use, potentially causing loss of imaging capability. In some cases, the system may need to be restarted to restore function temporarily. Philips has identified this issue in multiple Azurion models used in medical facilities.

GE HealthCare has identified a situation where the ApexPro CARESCAPE Telemetry Server (versions 5.0 and 6.0) can lose ECG and SpO2 monitoring data if the system loses network connection to the central monitoring station. This affects 14 units used in hospitals and clinical settings.

GE HealthCare identified a rare condition in CARESCAPE Telemetry Server v5.0 and v6.0 where a persistent network communication failure at the central monitoring station can result in loss of ECG and SpO2 (heart rhythm and blood oxygen) monitoring. The problem occurs only when the system is in a "NO COMM" or "OFF NETWORK" state at the central station.

A limited number of Medtronic 2x4 Pocket Adaptor Kits (Models 64001 and 64002) were labeled with incorrect Use-By-Dates. The affected kits are used with deep brain stimulation systems to treat parkinsonian tremor. No injuries have been reported.

Devicor Medical Products is recalling HydroMARK Breast Biopsy Site Marker Model 4010-02-15-T3 due to incorrect labeling on individual packages inside boxes. Some boxes labeled as T3 markers may contain packages labeled as T4 markers, which could lead to use of the wrong marker type during a breast biopsy procedure.

Certain Impella Controller (AIC) consoles contain electrical faults including alarm failures, power-path problems, and inaccurate motor sensing. Additionally, improper alignment between the purge cassette and motor drive can prevent the purge system from priming correctly, requiring users to switch to a backup console.

Medline distributed multiple spinal anesthesia and nerve block procedure kits containing Bupivacaine Hydrochloride in Dextrose Injection made by Huons Co. The anesthetic was recalled due to quality concerns, including problems with microbiology testing data and reports that the medication may not work as expected.

Halyard Purezero Ultraviolet Nitrile Exam Gloves in sizes XS through XL failed to meet chemical permeation performance standards, meaning they may not provide adequate protection against certain chemicals. This affects approximately 452,500 units distributed nationwide.

Abiomed identified that certain Automated Impella Controller (AIC) units have internal hardware issues that could affect device operation. These include cable and component positioning problems that may interrupt motor controls, cause startup failures, or prevent the device from booting properly. Abiomed is implementing hardware updates through its servicing process.

The proximal clasp on Bolton Medical's RelayPro Thoracic Stent-Graft System may disconnect from the outer control tube during use. This disconnection could prevent the stent graft from being released properly from its delivery system. The FDA has issued a labeling update to inform physicians and hospitals of this potential issue.

Fly By Jing Creamy Sesame Noodles (3.8 oz packets) may contain peanuts due to cross-contamination during production, even though peanuts are not listed on the label. This poses a serious risk to people with peanut allergies. The recall affects approximately 3,419 cases with best-by dates between October 15, 2026 and March 23, 2027.

AbbVie is recalling specific lots of PRED MILD (prednisolone acetate) eye drops because they failed stability testing. The affected product may not maintain its intended strength or safety over time. Two lots are involved, with an expiration date of August 2026.

AVEVA nicotine patches (14 mg) distributed by Rugby Laboratories have elevated levels of chemical impurities that exceed safety standards for shelf life. The issue was discovered during stability testing of specific lots. No injuries have been reported.