All Recalls

BD Kiestra ReadA modules may experience connectivity issues after a reboot, potentially delaying plate retrieval.

Datascope is recalling the Cardiosave Battery Charging Station due to a design flaw in the left bay that prevents proper battery charging.

Hitachi is recalling its Proton Beam Therapy System due to a software error that may cause inaccurate patient positioning during treatment.

EnHomee 10-Drawer Dresser (Model 55SCWMSCXLBR) poses tip-over and entrapment hazards to children if not wall-anchored; violates STURDY Act.

Andy & Evan is recalling children's pajama sets (sizes 2T–6X) due to flammability standard violation and serious burn hazard risk.

DriBiz is recalling Ammo Tabs desiccant tiles (Model AMT-010) that may fail to prevent moisture damage to firearms and ammunition, increasing malfunction risk.

Clark Associates is recalling 180 item numbers of Lancaster Table & Seating outdoor chairs and barstools due to legs that can bend or break, posing a fall hazard.

Fixwal 7-Drawer Dressers (55.1"L × 11.8"W × 31.5"H) sold on Amazon pose tip-over and entrapment hazards without wall anchoring.

PurSteam is recalling Elite Travel (PS-510) and Mighty Lil (PS-550) steamers with specific date codes due to risk of hot water expulsion and serious burn injury.

Dresbe LED Christmas Headbands (HB-052) recalled; easily accessible button cell batteries pose ingestion hazard to children.

Cobelae Busy Book model 2025-Q3-0702 recalled for detachable beads posing choking hazard.

Furnulem recalls five-drawer dressers (Model HK-DS-017-CL-5D-1-W) over tip-over and entrapment risk to children.

Little Cow Co. is recalling 9 oz soy wax candles in glass jars due to risk of cracking or breaking during use.

GM Gumili Wintergreen Essential Oil bottles lack required child-resistant packaging, posing poisoning risk to young children.

YITA is recalling 16-drawer dressers (Dextrus, ModFusion, Uforic, Yintatech, Yitahome) due to tip-over and entrapment hazards; wall anchoring required.

Lotus Joy Sweet Birch Essential Oil recalled for lack of child-resistant packaging; methyl salicylate poisoning risk.

Shintenchi 6-drawer dresser (model SHX12077-WH) recalled for tip-over and entrapment hazards; requires wall anchoring.

Semfri children's helmets (size M) sold at Walmart.com June–Nov 2025 fail safety standards and pose serious head injury risk.

Lola + The Boys is recalling five youth hooded clothing styles with drawstrings due to strangulation hazard in children.

Kitosun Submersible LED Lights recalled for easily accessible lithium coin batteries posing serious ingestion hazard to children.

Organic Zing Birch Essential Oil bottles lack required child-resistant packaging, posing poisoning risk to children.

Tippy Toes Apple Pear Banana baby food is recalled due to potential patulin contamination.

Fagron Sterile Services is recalling Thiamine HCl 500 mg injection due to a lack of assurance of sterility.

Remel is recalling Campy CVA Medium (R01272) due to low recovery of Campylobacter Jejuni on identified lots.

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

Scepter B62 fuel containers lack flame mitigation and child-resistant spouts, posing flash fire and burn risks.

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

Diagnostica Stago is recalling STA Liatest Free Protein S kits due to the risk of inaccurate test results for normal patient plasma levels.

React Health PHOENIX 5L Oxygen Concentrator recalled due to devices not meeting quality specifications.

Fresenius Kabi is recalling the Ivenix Infusion System LVP due to a risk of the cassette loading lever breaking during use.

Mays Chemical recalls 46,315 lbs of frozen pork boneless loins imported without U.S. reinspection; discard or return.

Pure Solutions recalling 1 fl oz sleep formula bottles due to undeclared milk allergen from bovine colostrum.

Coco's Italian Market is recalling Cannoli Making Kits due to undeclared wheat and milk allergens.

Prime Food Processing is recalling Dried Croaker Fish due to the risk of botulism from uneviscerated fish.

Northstar Rx LLC is recalling Pitavastatin Tablets, 2 mg (NDC 72603-479-01) due to a foreign 1 mg tablet found in bottles.

Exactech is recalling the Equinoxe Ergo Modular Impactor Handle due to a missing cross-pin that may cause device failure.

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

IBA PROTEUS 235 proton therapy systems may fail to stop beam delivery if external gating device signal is lost, risking patient mistreatment.

Pro Numb is recalling 5% Lidocaine Tattoo Numbing Spray due to cGMP manufacturing deviations.

B. Braun is recalling 21GA Winged Infusion Sets (Model 7M2802) due to potential needle tip dullness or breakage.

Howmedica Osteonics is recalling MICS3 Angled Sagittal Saw Attachments because external screws may loosen and detach during use.

On-X is recalling Model ONXMC-25/33 Mitral Heart Valve due to incomplete testing before distribution.

Kirkland Signature Mini Beignets are recalled due to undeclared hazelnut, posing a risk to those with hazelnut allergies.

Reser's Fine Foods is recalling Molly Kitchen's Tuna Salad due to undeclared fish allergen from incorrect lid labeling.

Karns Foods is recalling 8 oz Mini Dark Chocolate Raspberry Cups due to undeclared peanuts.

Tiki Bar Dark Chocolatey Peanut Butter & Pretzel is recalled due to an undeclared peanut allergen.

Beckman Coulter is recalling chemistry analyzers due to a software error that may cause system delays and impact patient diagnosis.

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

Medtronic is recalling MiniMed 780G insulin pumps (models MMT-1884, MMT-1886) running software 6.60-6.62 due to insulin delivery inaccuracies.

GE is recalling Centricity Universal Viewer software versions 5.0 and 7.0 due to a cybersecurity vulnerability that may expose user credentials.