Fisher Scientific recalls Sure-Vue Pipette (500/pack) due to temperature exposure during shipping from June 2021-August 2021, potentially reducing effectiveness. Affected units were shipped between June 1 and September 30, 2021.
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.
Fisher Scientific is recalling Sure-Vue Pipettes that were shipped between June 1 and September 30, 2021, because they may have been exposed to higher temperatures during shipping, which could reduce their effectiveness. This recall does not pose a safety risk but affects product performance.
The pipettes were shipped between June 1 and September 30, 2021, and may have been exposed to higher temperatures during transit. This exposure could impact the product's effectiveness, but it does not pose a safety risk like injury or fire.
Laboratory users who purchased the Sure-Vue Pipette (500/pack) with catalog number 23038015 between June 1 and September 30, 2021. Those using the pipettes for laboratory work may experience reduced effectiveness due to temperature exposure.
Check if your pipettes have catalog number 23038015 and were purchased between June 1 and September 30, 2021. The product is labeled as 'Sure-Vue Pipette, RPR Dispensing (500/PK).'
Verify the catalog number 23038015 and purchase date between June 1 and September 30, 2021.
The pipettes may have been exposed to higher temperatures during shipping from June 2021 to August 2021, which could reduce their effectiveness.
No, this recall is about potential reduced effectiveness, not safety risks like injury or fire.
Check for catalog number 23038015 and purchase dates between June 1 and September 30, 2021.
We’ve drafted a message you can send Fisher Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-1624-2022 — Fisher Scientific Fisher Scientific Hello, I own a Fisher Scientific that is covered by recall Z-1624-2022 from Fisher Scientific. 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.
