Morrison Medical OB KITs from June 2021-August 2021 may have been exposed to high temperatures, potentially reducing effectiveness. Consumers should check if their kit was manufactured during this period.
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.
Morrison Medical OB KITs produced between June 1 and September 30, 2021, were recalled due to potential temperature exposure during shipping. This could reduce the product's effectiveness but does not pose a safety risk to users.
The kits were exposed to higher temperatures during shipping from June 2021 to August 2021, which could reduce their effectiveness. This is not a safety hazard but may impact the product's intended use in medical settings.
Healthcare facilities that received Morrison Medical OB KITs between June 1 and September 30, 2021, are likely affected. Staff using these kits for obstetric care may be at risk if the product's effectiveness is compromised.
Check if your kit has the catalog number 0967NL and was purchased between June 1 and September 30, 2021. The product is packaged in a hard box sealed with cardboard.
Verify if your kit was manufactured between June 1 and September 30, 2021 using the catalog number 0967NL.
No, this recall is for potential reduced effectiveness due to temperature exposure, not a safety hazard.
Check for the catalog number 0967NL and if it was purchased between June 1 and September 30, 2021.
The recall does not require immediate action; check if your kit is affected and contact Morrison Medical if you have concerns.
We’ve drafted a message you can send Morrison Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1632-2022 — Morrison Medical Morrison Medical Hello, I own a Morrison Medical that is covered by recall Z-1632-2022 from Morrison Medical. 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.
