Medline Semi-Rigid Suction Liners (Medline) – Adverse Events (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medline Semi-rigid suction liners labeled as follows: a) SEMI RIGID SUCTION LINER, REF OR515; b) SEMI RIGID SUCTION LINER WITH TUBING, REF OR526K; c) SEMI RIGID SUCTION LINER WITH TUBING, REF OR527K; d) SEMI RIGID SUCTION LINER WITH TUBING, REF OR529K
Brand
MEDLINE INDUSTRIES, LP Northfield
Lot Codes / Batch Numbers
a) OR515: UDI/DI 10884389968093, Lot Numbers: 93023082618C, 93023082730C, 93023090602C, 93023090902C, 93023091309C, 93023091409C, 93023091428C, 93023091506C, 93023091609C, 93023091806C, 93023093A10C, 93023098426C, 93023098623C, 93023098811C, 93023099605C, 93023099705C, 93023099806C, 93023099826C, 93023102613C, 93023102718C, 93023102815C, 93023102920C, 93023103015C, 93023103120C, 93023103316C, 93023103B08C, 93023106628C, 93023106721C, 93023107028C, 93023107225C, 93023108512C, 93023108712C, 93023112721C, 93023112828C, 93023113027C, 93023113327C, 93023113626C, 93023113C12C, 93023116906C, 93023117013C, 93023117106C, 93023117118C, 93023117212C, 93023117301C, 93023117317C, 93023117401C, 93023117420C, 93023117506C, 93023117512C, 93023117618C, 93023117721C, 93023117806C, 93023117917C, 93023118018C, 93023123D02C, 93024013602D, b) OR526K: UDI/DI 10888277253087, Lot Numbers: 93023103026C, 93023103126C, 93023106626C, 93023113621C, 93023113725C, 93023116708C, 93023117809C, 93023117920C, 93023118025C, c) OR527K: UDI/DI 10888277253094, Lot Numbers: 93023091427C, 93023093227C, 93023093327C, 93023098827C, 93023106629C, 93023113615C, 93023116708C, 93023117815C, 93023117817C, 93023117915C, d) OR529K: UDI/DI 10888277253100, Lot Numbers: 93023091709C, 93023091824C, 93023092709C, 93023098824C, 93023101409C, 93023103209C, 93023103309C, 93023106629C, 93023116710C, 93023117815C, 93023117922C, 93023118022C, 93023124606C.
Products Sold
a) OR515: UDI/DI 10884389968093, Lot Numbers: 93023082618C, 93023082730C, 93023090602C, 93023090902C, 93023091309C, 93023091409C, 93023091428C, 93023091506C, 93023091609C, 93023091806C, 93023093A10C, 93023098426C, 93023098623C, 93023098811C, 93023099605C, 93023099705C, 93023099806C, 93023099826C, 93023102613C, 93023102718C, 93023102815C, 93023102920C, 93023103015C, 93023103120C, 93023103316C, 93023103B08C, 93023106628C, 93023106721C, 93023107028C, 93023107225C, 93023108512C, 93023108712C, 93023112721C, 93023112828C, 93023113027C, 93023113327C, 93023113626C, 93023113C12C, 93023116906C, 93023117013C, 93023117106C, 93023117118C, 93023117212C, 93023117301C, 93023117317C, 93023117401C, 93023117420C, 93023117506C, 93023117512C, 93023117618C, 93023117721C, 93023117806C, 93023117917C, 93023118018C, 93023123D02C, 93024013602D; b) OR526K: UDI/DI 10888277253087, Lot Numbers: 93023103026C, 93023103126C, 93023106626C, 93023113621C, 93023113725C, 93023116708C, 93023117809C, 93023117920C, 93023118025C; c) OR527K: UDI/DI 10888277253094, Lot Numbers: 93023091427C, 93023093227C, 93023093327C, 93023098827C, 93023106629C, 93023113615C, 93023116708C, 93023117815C, 93023117817C, 93023117915C; d) OR529K: UDI/DI 10888277253100, Lot Numbers: 93023091709C, 93023091824C, 93023092709C, 93023098824C, 93023101409C, 93023103209C, 93023103309C, 93023106629C, 93023116710C, 93023117815C, 93023117922C, 93023118022C, 93023124606C.
MEDLINE INDUSTRIES, LP Northfield is recalling Medline Semi-rigid suction liners labeled as follows: a) SEMI RIGID SUCTION LINER, REF OR515; b) SE due to Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 0. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
Recommended Action
Per FDA guidance
Medline Industries issued a MEDICAL DEVICE RECALL notice to its consignees on 06/27/2024 via US mail and email. The notice explained the problem with the device, potential risk to the patient, and requested the consignee immediately check their stock for the affected item number and the affected lot numbers and destroy any affected inventory. Distributors were directed to notify their customers of the recall and request the affected products be destroyed. For questions: contact the Recall Department at 866-359-1704 or recalls@medline.com.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026