Getinge recalls Flow-c Anesthesia Systems with serial numbers 4003-5050 for potential suction switch cracks that could prevent suction activation, risking patient harm during anesthesia procedures.
Potential for crack to form on the on/off switch of the suction unit, which may result in an unreasonable risk of harm to the patient. In the worst case, the switch can break, preventing the suction unit from being activated.
Getinge is recalling anesthesia systems that could develop cracks in the suction switch, potentially preventing suction from working during surgery. This could cause serious harm to patients if the switch breaks while under anesthesia.
The suction unit's on/off switch can crack under normal use, which might break the switch and stop suction from working. This could prevent critical airway support during anesthesia, risking patient injury or death.
Anesthesia providers using the Flow-c Anesthesia System with specific serial numbers are affected. Patients undergoing surgery with this equipment are at risk if the suction switch cracks.
Check the serial numbers listed: 4003, 4777, 4783, 5024, 5025, 5026, 5027, 5028, 5043, 5044, 5045, 5046, 5047, 5048, 5049, 5050. The product was sold by Getinge Usa Sales Inc.
Inspect the on/off switch for cracks or damage before use. If cracked, stop using the system immediately.
Product code/REF number: 6887700
Serial numbers 4003, 4777, 4783, 5024, 5025, 5026, 5027, 5028, 5043, 5044, 5045, 5046, 5047, 5048, 5049, 5050.
The recall record does not mention a remedy or fix.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-1278-2022 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-1278-2022 from Getinge. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
