All Product Recalls

Gold Star Distribution Recalls Feminine Hygiene Products Due to Rodent Exposure

Potential exposure of rodents and rodent activity in the distribution center.

Haleon Recalls parodontax Mouthwash Over Labeling Issues

Haleon recalled 84,764 bottles of parodontax Mouthwash on December 26, 2025. The product may have missing or illegible lot and expiration dates. Consumers should stop using the mouthwash immediately.

Gold Star Distribution Recalls Liquid DayQuil 12/8oz for CGMP Issues (2025)

CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

Gold Star Distribution Recalls Vaseline and Other Petroleum Jelly Products for CGMP Violations (2025

CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

Gold Star Distribution Recalls Excedrin Migraine 2's 25 CT Over Rodent-Contamination Risk (2026)

CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

Gold Star Distribution Motrin 2's Disp.-50ct Recall Active Over Rodent Exposure

CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

GOLD STAR DISTRIBUTION TUMS 12-Count Recall 2026 for Rodent-Contamination CGMP Deviations

CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

Colgate and Crest Toothpaste Recall 2025 by Gold Star Distribution for CGMP Deviations

CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

Gold Star Distribution Recalls Pepto Bismol 32-Count in 2025 Over CGMP Sanitation Violations

CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.

Zimmer Tourniquet Systems Recalled Due to Screen Freezing Hazard

Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternate device is located.

Medline Recalls Medical Kits Over Seal Integrity Issues

Medline Industries, LP recalled 7,380 medical convenience kits on December 24, 2025. The recall affects the PowerGlide Dressing Change Kit and Central Line Tray with ChloraPrep swabsticks. An open seal on packaging may compromise sterility and patient safety.

Medline Suction Catheter Kits Recalled Due to Serious Health Risk

Medline Recalls Medical Kits Due to Seal Integrity Issues

Medline Industries, LP recalled 7,570 medical convenience kits on December 24, 2025. The kits contain BD ChloraPrep Triple Swabsticks with an open seal risk. Healthcare providers and patients should stop using these kits immediately.

Medline Recalls Sterile Resection Kits Due to Open Seal Hazard

Medline Industries, LP announced a recall of 216 kits packaged as Sterile Resection Packs on December 24, 2025. The kits contain BD ChloraPrep Triple Swabsticks that may have an open seal. The recall affects healthcare providers and patients nationwide.

GE Healthcare Omni Legend Recalled Due to Image Artifact Risk

Southern Rocklobster LTD Recalls Frozen Abalone Over Listeria Risk

Zimmer Tourniquet Systems Recalled Due to Screen Malfunction

Zimmer Surgical Inc recalled 206 A.T.S. 5000TS Tourniquet Systems on December 24, 2025. The device can freeze or become unresponsive in certain non-English language settings. This issue may delay patient care during emergencies.

Medline Recalls Medical Kits Over Hazardous Packaging Seal

Medline Industries, LP recalled 120 medical convenience kits on December 24, 2025. The kits contain BD ChloraPrep Triple Swabsticks with potentially open seals. This recall affects products distributed nationwide in the U.S.

Medline Recalls Medical Kits Over Open Seal Hazard

Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.

Medline Recalls Blood Culture Kits Due to Open Seal Hazard

Medline Industries, LP recalled 4,300 blood culture kits on December 24, 2025. The recall affects kits containing BD ChloraPrep Triple Swabsticks with packaging that may exhibit an open seal. This defect poses a high risk to patient safety.