Bayer recalls MEDRAD Twist & Go Disposable Syringes due to labeling error with Mark 7 Arterion system. Affected units may be misused if not properly identified. Contact for details.
Labeling error: MEDRAD Mark 7 Arterion Injection System Syringes (ART 700 SYR) labeled as Twist & Go Syringes (TAG 150 SYR)
Bayer is recalling MEDRAD Twist & Go Disposable Syringes (150 mL) because they are incorrectly labeled as part of the Mark 7 Arter:ion Injection System. This labeling error could lead to improper use if the syringe is not correctly identified with the right system.
The syringe is labeled as a Twist & Go Syringe (TAG 150 SYR) but is part of the Mark 7 Arterion Injection System (ART 700 SYR). This labeling error could cause confusion if the syringe is not correctly identified with the right system, potentially leading to improper use.
Healthcare professionals using the syringe with the MEDRAD Mark 7 Arterion Injection System may be affected. Those who have the syringe with batch number 8415317 are most at risk.
Check for the batch number 8415317 on the syringe. The syringe is part of the MEDRAD Mark 7 Arterion Injection System and is labeled as a Twist & Go Syringe (TAG 150 SYR).
Look for the batch number 8415317 on the syringe to confirm if it is affected.
The syringe is labeled as a Twist & Go Syringe (TAG 150 SYR) but is part of the Mark 7 Arterion Injection System (ART 700 SYR).
Check for the batch number 8415317 on the syringe. The syringe is part of the MEDRAD Mark 7 Arterion Injection System and is labeled as a Twist & Go Syringe (TAG 150 SYR).
The recall record does not specify a remedy, so contact Bayer Medical Care for further instructions.
We’ve drafted a message you can send Bayer Medical Care to request your refund or repair — edit it as you like.
Subject: Recall Z-0199-2022 — Bayer Medical Care Bayer Medical Care Hello, I own a Bayer Medical Care that is covered by recall Z-0199-2022 from Bayer Medical Care. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
