All Recalls

Medacta is recalling Short Monobloc Stem Broaches for the Shoulder System due to a risk of humerus fracture during surgery.

Medline recalls convenience kits with Swan-Ganz catheters over leak/breakage risk.

High Valley Orchard Chocolate Covered Raisins are recalled due to undeclared peanuts caused by a mis-packaging error.

Treatlife smoke and CO detectors are recalled because they may fail to alert users to a fire, posing a risk of injury or death.

Amana air conditioners and heat pumps are recalled due to a fire and burn hazard caused by a faulty heating element.

Honlyne LED party favors (Model HON-302HE) are recalled due to a button cell battery ingestion hazard that can cause serious injury or death.

Kith is recalling children's loungewear sets due to a violation of federal flammability standards, posing a risk of serious burn injuries.

Small Fish Montessori Busy Board (model 2512JX02) is recalled due to a magnet ingestion hazard that can cause serious injury or death.

Raychy children's light-up sneakers are recalled due to a serious battery ingestion hazard from accessible lithium coin batteries.

Lomi Roll-On Waxing Kits are recalled because the warmer's power cord can overheat, posing fire, burn, and shock hazards.

Sunderwell XW-A17 youth electric ATVs are recalled for missing brake lights, which poses a crash hazard and violates federal safety standards.

Elevate Oral Care is recalling Povi-One 10% Povidone-Iodine Oral Antiseptic due to sub-potency.

Boston Scientific recalls Intera 3000 pump over drug pathway leakage risk.

Medline recalls convenience kits with 10mL syringes over unapproved design changes.

Abiomed recalls Impella CP introducer kit over thrombus risk.

Sun Pharmaceutical is recalling 6mg Perampanel CIII tablets due to a labeling mix-up where bottles may contain 10mg tablets.

Camber Pharmaceuticals is recalling Lacosamide 100mg tablets due to a potential mix-up with Selexipag 1000 mcg tablets.

ANI Pharmaceuticals is recalling Hydroxyzine Hydrochloride Oral Solution, 10 mg/5 mL, due to the presence of a foreign substance.

Philips is recalling Telemetry Monitor 5500 units due to a potential reset error that prevents connection to the central monitoring system.

IPG Medical is recalling the Thuvera Laser Console due to a software anomaly that may cause a false error code 5018 display.

Medline recalls convenience kits with recalled lidocaine and bupivacaine injections due to supplier quality issues.

GE Healthcare is recalling the AW Server 3.2 ext.6.5 image processing system due to a software error that may display the wrong patient's data.

Medtronic recalls Octopus Evolution Tissue Stabilizer over incorrect tubing assembly.

Surgify Halo 3.0 mm Extendable drill recalled over burr breakage risk during spinal surgery.

Stryker is recalling the InZone Detachment System due to premature battery drain that may prevent coil detachment during medical procedures.

Direct Rx is recalling 30 mg Duloxetine Delayed-Release capsules due to N-nitroso-duloxetine impurity levels exceeding FDA limits.

Acumed is recalling various hexalobe screws used in wrist fixation systems due to a risk of the screws breaking during use.

Amgen recalls Corlanor and Sensipar tablets over foreign substance contamination.

Zimmer recalls Off-Axis Shoulder Reamer Guide Model 110040240 due to breakage risk.

PFM Medical is recalling Multi-Snare Set catheter devices due to a failure to meet biocompatibility requirements for in-vitro cytotoxicity.

Ventec is recalling the VOCSN+Pro respiratory system because a damaged battery may prevent the backup alarm from sounding during power loss.

Major Pharmaceuticals is recalling 0.2 mg Methylergonovine Maleate Tablets due to subpotency.

Ajanta Pharma is recalling Fenofibrate Capsules, USP 200 mg, due to manufacturing process deviations.

Philips recalls Avalon Fetal Monitor FM20 over speaker connector assembly issue causing cable pull-out and loss of speaker output.

Intuitive Surgical is recalling the Da Vinci surgical system E-brake retainer pin due to a risk of uncontrolled motion and patient injury.

TMJ Solutions is recalling custom temporomandibular joint implants due to incorrect components causing a poor fit and potential open bite.

Arizer is recalling Solo III portable vaporizers due to fire and burn hazards affecting specific serial prefixes and UPC 628078802274.

BABESIDE doll and stroller sets are recalled due to a choking hazard from small parts that violate federal safety standards.

GOPO Toys is recalling pull string teething toys due to a serious choking hazard caused by strings that violate federal safety standards.

Joolz is recalling Aer2 car seat adapters because they can fail to attach to the stroller, posing a fall hazard to children.

CooCooBaby is recalling Classic and Deluxe baby loungers due to suffocation and fall hazards that violate federal infant sleep safety standards.

Michley children's pajamas are recalled for failing to meet federal flammability standards, posing a serious burn injury or death risk.

Veseacky children's pajama sets are recalled for violating federal safety standards, posing a serious burn injury or death risk to children.

Keystone recalls 20% benzocaine gels from 7 brands over defective container seals.

HeartMate 3 LVAS kits recalled due to backup battery failures.

Staar Surgical is recalling Version 8.00 of its ICL Calculation Software due to a coding error affecting toric lens orientation diagrams.

Inspire Medical recalls Respiratory Sensing Lead Model 4340 due to incorrect Use By dates that may cause premature revision surgery.

BD is recalling Connecta Luer-Lok stopcocks due to a potential connection failure at Port C when using plastic luer-lok syringes.

Merit Medical is recalling various Splashwire Hydrophilic Guide Wire models due to unsealed pouches that may compromise device sterility.

Par Health is recalling Buprenorphine HCl Injection due to crystallization identified as Buprenorphine free base.