{"id":970777,"date":"2026-06-04T14:35:02","date_gmt":"2026-06-04T18:35:02","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/haleon-issues-voluntary-nationwide-recall-of-gas-x-extra-strength-softgels-125mg-120-ct-and-72-ct\/"},"modified":"2026-06-04T14:35:02","modified_gmt":"2026-06-04T18:35:02","slug":"haleon-issues-voluntary-nationwide-recall-of-gas-x-extra-strength-softgels-125mg-120-ct-and-72-ct","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/haleon-issues-voluntary-nationwide-recall-of-gas-x-extra-strength-softgels-125mg-120-ct-and-72-ct\/","title":{"rendered":"Haleon Issues Voluntary Nationwide Recall of Gas-X Extra Strength Softgels 125mg, 120 ct. and 72 ct."},"content":{"rendered":"

<\/p>\n

Haleon Issues Voluntary Nationwide Recall of Gas-X Extra Strength Softgels 125mg, 120 ct. and 72 ct.<\/b><\/p>\n

WARREN, N.J.–(BUSINESS WIRE<\/a>)–
\nHaleon (NYSE: HLN) is voluntarily recalling four lots of Gas-X Extra Strength Softgels 125mg, 120 ct. and 72 ct. distributed on or about April 13, 2026 to the consumer level. The lots are being recalled due to potential contamination with a diluted propylene glycol-based coolant from a machine leakage during the packaging process.<\/p>\n

This press release features multimedia. View the full release here: https:\/\/www.businesswire.com\/news\/home\/20260604056780\/en\/<\/a><\/p>\n

\"Gas-X<\/p>\n

Gas-X Extra Strength Softgels (120 ct.) Front of Carton<\/p>\n<\/div>\n

\nThere is a potential that ingestion of the Softgels contaminated with the diluted propylene glycol-based coolant may result in adverse events such as nausea, vomiting, abdominal pain and diarrhea.<\/p>\n

\nTo date, Haleon has not received any reports of adverse events related to this recall.<\/p>\n

\nGas-X Extra Strength Softgels are indicated to quickly break up gas bubbles in the digestive tract and relieve pressure, bloating, and discomfort. Gas-X Extra Strength Softgels are uniquely identified as a green capsule and found in packaging with a green band.<\/b>Only the lots in the table below are impacted.<\/b>No other lots of Gas-X Extra Strength, Gas-X Ultra, Gas-X Maximum and Gas-X Ultimate are impacted by this recall.<\/b><\/p>\n\n\n\n\n
\n

Product<\/b><\/p>\n<\/td>\n

\n

UPC<\/b><\/p>\n<\/td>\n

\n

Lot Number<\/b><\/p>\n<\/td>\n

\n

Expiry Date<\/b><\/p>\n<\/td>\n

\n

Dates of Distribution<\/b><\/p>\n<\/td>\n<\/tr>\n

\n

Gas-X Extra Strength Softgels<\/i><\/p>\n

(120 ct.)<\/i><\/p>\n<\/td>\n

\n

\n300674350419<\/p>\n<\/td>\n

\n

\nTL8K<\/p>\n

\nYH9X<\/p>\n

\nYH9Y<\/p>\n<\/td>\n

\n

\n30 Nov 2028<\/p>\n

\n30 Nov 2028<\/p>\n

\n30 Nov 2028<\/p>\n<\/td>\n

\n

\n13 Apr 2026 \u2013 05 May 2026<\/p>\n<\/td>\n<\/tr>\n

\n

Gas-X Extra Strength Softgels<\/i><\/p>\n

(72 ct.)<\/i><\/p>\n<\/td>\n

\n

\n300439005721<\/p>\n<\/td>\n

\n

\nX78N<\/p>\n<\/td>\n

\n

\n30 Nov 2028<\/p>\n<\/td>\n

\n

\n05 May 2026 \u2013 14 May 2026<\/p>\n<\/td>\n<\/tr>\n<\/table>\n

\nThis recall is being conducted with the knowledge of the U.S. Food and Drug Administration (FDA).<\/p>\n

\nHaleon is notifying its distributors and customers by letter, email, and phone notification, and is arranging for the return of all recalled products.<\/p>\n

\nConsumers who have purchased Gas-X Extra Strength Softgels on or after April 13, 2026, should review the lot number. If the lot number matches those impacted by this recall, stop taking the product immediately and contact the Haleon Consumer Relations team at +1-800-245-1040 (Monday through Friday 8 a.m. to 6 p.m. ET), or via mystory.us@haleon.com<\/a> or https:\/\/haleon.help\/en-us\/contact-form<\/a> to arrange for return of the product and request reimbursement.<\/p>\n

\nConsumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product. They should also report any adverse events to our Consumer Relations Team at +1-800-245-1040 (Monday through Friday 8 a.m. to 6 p.m. ET) or via mystory.us@haleon.com<\/a> or https:\/\/haleon.help\/en-us\/contact-form.<\/a><\/p>\n

\nAdverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.<\/p>\n