Skip to content
Use caution Drug recall · FDA · Published March 16, 2020

The Medicine Shoppe Recalls Gentamicin Irrigation Due to Sterility Risk

The Medicine Shoppe Pharmacy recalls specific Gentamicin 80mg/60mL irrigation containers due to a lack of assurance of sterility.

🇺🇸 FDA recall #D-1072-2020DrugThe Medicine Shoppe Pharmacy ›
Take action

Contact the company

Recalling firmThe Medicine Shoppe Pharmacy3524 B Tamiami Trl · Port Charlotte, FL 33952-8100
✎ GovInfoNow plain-language explainer

What happened, in plain English

The Medicine Shoppe Pharmacy is recalling Gentamicin 80mg/60 mL Irrigation containers because there was a lack of assurance of sterility. This recall affects a small quantity of product distributed in Florida. The record does not specify the exact remedy for consumers other than noting the lot number and discard date. Read more at govinfonow.com/recall/37316-the-medicine-shoppe-recalls-gentamicin-irrigation-due-to-sterility-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/37316-the-medicine-shoppe-recalls-gentamicin-irrigation-due-to-sterility-risk · Updated October 11, 2026 · FDA enforcement record: FDA #D-1072-2020

Cite this page

“The Medicine Shoppe Recalls Gentamicin Irrigation Due to Sterility Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/37316-the-medicine-shoppe-recalls-gentamicin-irrigation-due-to-sterility-risk. Based on FDA recall #D-1072-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1072-2020%22&limit=1).

Why it’s dangerous

The primary hazard is a lack of assurance of sterility, which means the containers may not be free from microorganisms. Using non-sterile irrigation solutions can introduce infections or other complications during medical procedures.

Who’s affected

Patients or healthcare providers in Florida who purchased Gentamicin 80mg/60 mL Irrigation from The Medicine Shoppe Pharmacy. Individuals using this specific irrigation solution are at risk of exposure to non-sterile product.

How to tell if you have this one

Look for Gentamicin 80mg/60 mL Irrigation containers distributed in Florida. The specific lot number is 7016542, and the product should be discarded after 01/12/2021.

  • Brand
    The Medicine Shoppe Pharmacy
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Lot Number

    Verify if your Gentamicin 80mg/60 mL Irrigation containers have lot number 7016542.

  2. Discard Product

    Discard the recalled containers after 01/12/2021 if you possess them.

    01/12/2021

Where it went and when

Where it was distributed

Distributed in Florida.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “Florida” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida.

Recall timeline

FDA terminated this recall 2.7 years after the firm started it.

1. Firm started the recall: Mar 16, 202012. FDA classified it Class II: Mar 31, 202023. Published in FDA’s Enforcement Report: Apr 8, 202034. FDA terminated the recall: Dec 8, 2022420202022
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

Similar recalls

Latest drug recalls

Keep exploring

Where this comes from

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.

  • Official source: FDA Recall #D-1072-2020 (March 16, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1072-2020 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA