Cardinal Health recalls two sterile procedure packs due to potential contamination in recalled components. Affected packs have specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Cardinal Health is recalling two types of sterile procedure packs because they contain recalled components that may be contaminated. This could lead to infection risks during medical procedures if used improperly.
The packs contain equipment drapes, table covers, and surgical room turnover kits that may have been contaminated. Using these components without proper sterilization could lead to infections during medical procedures.
Healthcare providers using the recalled procedure packs are most at risk. Patients receiving procedures with these packs could face infection risks if the equipment is contaminated.
Check for lot numbers: SANV1PIFSB (Lot #67711, expires 3/1/2026) or SAN12BHGT1 (Lot #13526, expires 3/1/2024). These packs are sold by Medstar hospitals.
Look for lot numbers and expiration dates on the pack to confirm if it's recalled.
The recall states the packs contain recalled components that may be contaminated, so they should not be used until the manufacturer provides a remedy.
Check for lot numbers: SANV1PIFSB (Lot #67711, expires 3/1/2026) or SAN12BHGT1 (Lot #13526, expires 3/1/2024). These packs are sold by Medstar hospitals.
The recall does not specify a remedy, so contact Cardinal Health directly for instructions.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0088-2024 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0088-2024 from Cardinal Health. 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.
