Mckesson Medical-Surgical recalls Fischer Cone Biopsy Excisors with model 900-157 that may have been affected by temperature excursions between June and August 2021, potentially reducing effectiveness.
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.
Mckesson Medical-Surgical is recalling Fischer Cone Biopsy Excisors with model number 900-157 that were sold between June 1 and September 30, 2021. These devices may have been exposed to higher temperatures during shipping, which could reduce their effectiveness. Affected users should check if their device was sold in the specified timeframe and contact the manufacturer for guidance.
The devices may have been exposed to higher temperatures during shipping from June to August 2021, which could reduce their effectiveness. This is a potential issue for medical procedures requiring precise biopsy sampling.
Healthcare facilities that purchased the Fischer Cone Biopsy Excisor model 900-157 between June 1 and September 30, 2021. Medical staff using these devices for biopsies are most at risk if the product's effectiveness is compromised.
Check for the model number 900-157 on the device. The product was sold between June 1 and September 30, 2021, and may have been affected by temperature excursions during shipping.
Look for the model number 900-157 on the device to confirm if it is affected.
Reach out to Mckesson Medical-Surgical for guidance on whether the device needs replacement or adjustment.
The devices may have been exposed to higher temperatures during shipping from June to August 2021, which could reduce their effectiveness.
Model number 900-157.
Between June 1 and September 30, 2021.
We’ve drafted a message you can send Fischer to request your refund or repair — edit it as you like.
Subject: Recall Z-1612-2022 — Fischer Fischer Hello, I own a Fischer that is covered by recall Z-1612-2022 from Fischer. 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.
