Baxter Healthcare recalls specific laryngoscope models due to packaging error. Affected units include MAC F/O Laryngoscope and related sets with product codes 69061, 69696, and 69696-LED. No action needed as the hazard is packaging-related.
Packaging error.
Baxter Healthcare is recalling certain laryngoscope models due to a packaging error. This does not pose a safety risk to users and requires no action.
The recall is for a packaging error, meaning the product codes and lot numbers listed may not match the actual items received. However, this does not create a safety hazard for users.
Healthcare professionals using the specific laryngoscope models with product codes 69061, 69696, or 69696-LED are likely affected. No one is at risk from this packaging error.
Check for product codes 69061, 69696, or 69696-LED on the packaging or label. The lot code 21-056 is also associated with these units.
Look for product codes 69061, 69696, or 69696-LED on the packaging or label.
No action is needed as this is a packaging error recall that does not pose a safety risk.
Product codes 69061, 69696, and 69696-LED are affected, with lot code 21-056.
No, this packaging error does not create a safety hazard for users.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1288-2022 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-1288-2022 from Baxter Healthcare. 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.
