Microbiolog: KWIK-STIK 2-Pack with incorrect lot number 218-234-4 printed on foil pouch. Recalled due to misprint risk of using wrong lot number.
The incorrect lot number was printed on the foil pouch that the KWIK-STIK" is placed in. All foil pouches for lot 318-234-4 have the lot number misprinted as 218-234-4. The correct lot number was printed on the KWIK-STIK" canister label and KWIK-STIK" device label.
Microbiologics is recalling KWIK-STIK 2-Packs with a misprinted lot number on the foil pouch. This could lead to using the wrong product if the incorrect lot number is mistaken for the correct one.
The foil pouch has the wrong lot number printed as 218-234-4 instead of the correct 318-234-4. This misprint could cause confusion when verifying the product's lot number, but it does not pose a direct safety risk.
Users of KWIK-STIK 2-Packs with lot number 318-234-4 on the canister label. Those who rely on the lot number for product verification are most at risk.
Check the canister label and device label for lot number 318-234-4. The foil pouch may show lot number 218-234-4 instead.
Verify the lot number on the KWIK-STIK canister label is 318-234-4.
Confirm the lot number on the KWIK-STIK device label matches 318-234-4.
The foil pouch has the incorrect lot number printed as 218-234-4 instead of the correct 318-234-4.
Check the canister label and device label for lot number 318-234-4. The foil pouch may show lot number 218-234-4.
The recall does not require action; verify the lot number on the labels to ensure it's correct.
We’ve drafted a message you can send Microbiologics to request your refund or repair — edit it as you like.
Subject: Recall Z-0581-2022 — Microbiologics Microbiologics Hello, I own a Microbiologics that is covered by recall Z-0581-2022 from Microbiologics. 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.
