All Recalls

Macleods Pharma recalls Levothyroxine Sodium 150 mcg tablets (NDC 33342-401-44) nationwide due to subpotency.

The Lantern Knee System drill plate is recalled due to a manufacturing error that may cause excessive bone cuts during surgery.

Medtronic is recalling MiniMed 780G insulin pumps (models MMT-1884, MMT-1886) over software defects that may cause inaccurate insulin delivery.

Straumann recalls Custom Abutment Ti for Straumann RC due to material mix-up.

AMO is recalling TECNIS Eyhance IOLs with Simplicity Delivery System (model DIB00) because the lens may fail to unfold properly.

Koven Technology is recalling the BiDop 3 Pocket Doppler due to unauthorized fetal indication labeling.

I.T.S. is recalling Headless Compression Screw System components due to updated MRI safety testing showing higher temperature risks.

Handy Solutions Neck & Shoulders Heating Pad (Model 25607) may overheat and cause burns if folded or placed under the body.

Western Mixers recalls Chilli Spanish Peanuts (First Street 11 oz, Treasured Harvest 25 lb) due to possible glass contamination.

Radnostix is recalling Sodium Iodide I-131 Kit capsule packs due to failed product specifications.

Erbe USA recalls Flexible Cryoprobes because probes may rupture or burst during use.

Olympus recalls endoscope valves MAJ-1444 and MAJ-1443 over reprocessor incompatibility.

GE Medical Systems is recalling Imactis CT-Navigation System (Models E85101LA, E85101LP) due to potential needle trajectory/tip position discordance.

The full list of affected model numbers and serial ranges is available on the CPSC recall page.

Amazon is recalling Basics Camping Folding Pocket Knives due to a laceration hazard caused by a faulty blade folding mechanism.

Tainoki is recalling Noah, Owen, and Warren office chairs because the base can bend, posing a fall hazard.

Goregent infant walkers are recalled for failing to meet federal safety standards, posing a serious fall and injury hazard to infants.

Aisstxoer adult bike helmets (model GH018L) are recalled for failing federal safety standards, posing a serious head injury risk.

Specialized is recalling all Turbo Como SL electric bicycle forks due to a fatigue crack that poses a fall hazard.

Lifetime Brands is recalling BUILT LUUM light up tumblers due to choking and battery ingestion hazards.

Somerset Therapeutics is recalling Dexamethasone Sodium Phosphate Injection (NDC 70069-025-10/01) due to out-of-specification impurities at expiry.

Datascope is recalling the Cardiosave battery charging station due to a screw defect in the left bay that prevents proper charging.

Elekta is recalling Leksell Gamma Knife Perfexion, Icon, and Esprit systems due to potential adapter misalignment during radiation delivery.

LeMaitre Vascular is recalling the Artegraft Vascular Graft due to a labeling mix-up on the outer packaging.

ConvaTec recalls EsteemBody drainable pouches over possible leakage from a manufacturing issue.

Hologic is recalling the Aptima HPV Assay due to the potential for the test to generate invalid or false negative results.

Stryker is recalling Cub Pediatric Crib Model FL19H over missing access door warning labels.

Diagnostica Stago is recalling the STA Liatest D-Di kit due to a positive bias in D-Dimer measurements that may cause inaccurate test results.

Zydus Pharmaceuticals is recalling Icosapent Ethyl Capsules due to oxidation, which can cause capsule melting and discoloration.

Cardinal Health is recalling Webcol Alcohol Prep Pads (200-count boxes) due to microbial contamination that may pose infection risk.

Welch Allyn is recalling the Spot Vision Screener VS100 (software v3.2.0.1) due to a screen flickering issue that may trigger seizures.

Frito-Lay recalls Miss Vickies Spicy Dill Pickle chips 8 oz bags for undeclared milk allergen.

Taro Pharmaceuticals is recalling Children's Ibuprofen Oral Suspension 100 mg/5mL (120 mL) due to gel-like masses and black particles.

GE recalls Centricity Universal Viewer software over credential exposure risk.

Playground swing seats (model 999604) are being recalled due to a fall hazard caused by potential rivet failure.

Abbott is recalling ID NOW Influenza A & B 2 test kits (Model 427-000) due to an increased rate of invalid results.

Insulet is recalling Omnipod 5 Pods due to a cannula defect that can cause insulin under-delivery and severe health risks.

17 Stories 14-Drawer dressers are recalled due to tip-over and entrapment hazards that violate federal safety standards.

ProRider is recalling various bicycle helmets that fail federal safety standards, posing a serious risk of head injury or death in a crash.

LIVEHOM 11-Drawer Dressers are recalled due to tip-over and entrapment hazards that pose a risk of serious injury or death to children.

Stoney Games is recalling Kluster magnet chess games due to a serious magnet ingestion hazard that can cause severe internal injury or death.

Medline is recalling cardiac procedure kits to clarify that the included chest drainage units are intended for adult patients only.

Medline is recalling Medcrest surgical gowns due to fabric delamination risks that may lead to infection or delays in patient care.

Lutronic is recalling CLARITY II Laser System (Model 1110200210) due to sparking and burn hazard.

Rising Pharmaceuticals is recalling Temozolomide Capsules 5mg (NDC 16571-816-51) due to failed impurities and degradation specifications.

Mylan is recalling Amnesteem Isotretinoin 40 mg capsules (NDC 0378-6614-93) due to failed dissolution specifications.

Radnostix is recalling Sodium Iodide (I-131) Therapeutic Oral Solution due to the presence of particulate matter.

Artelon FlexBand Dynamic Matrix recalled over failed endotoxin testing.

Beckman Coulter recalls DxC 700 AU and AU5800 analyzers over software delay risk.

HealthCast is recalling Vital Sync software due to a failure to transmit or receive critical patient bedside monitor alarms.