CLASS II Device recall · Reported 18 Aug 2021 · FDA Enforcement Report

Medline Knee Arthroscopy Kit, convenience kit recalled

Medline Industries is recalling Medline Knee Arthroscopy Kit, convenience kit, distributed nationwide in the US. The recall was initiated on 1 Jul 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 19WBA897, Exp. 2020-12-31, GTIN (01)10193489225143.
Quantity recalled286 kits total for all products

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-2232-2021
FDA event ID
88268
Recalling firm
Medline Industries, Northfield, IL
Classification
Class II
Status
Terminated
Recall initiated
1 Jul 2021
FDA classified
9 Aug 2021
Reported
18 Aug 2021
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

1 Jul 2021Recall initiated by company
9 Aug 2021Classified by FDA+39 days
18 Aug 2021Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The kits may contain an expired component.

Product as listed by the FDA

Medline Knee Arthroscopy Kit, convenience kit, REF DYNJ902838C, containing expired component NaCl 3000mL Irrigation Bag (exp. date 08/01/2020).

Where it was distributed

US Nationwide distribution in the states of MN, NE, and PA.

Nationwide MinnesotaNebraskaPennsylvania

Questions about this recall

Is Medline Knee Arthroscopy Kit, convenience kit recalled?

Yes. Medline Industries recalled Medline Knee Arthroscopy Kit, convenience kit on 1 Jul 2021. The recall is Class II and its status is Terminated. Recall number Z-2232-2021.

Why was it recalled?

The kits may contain an expired component.

Which lots are affected?

Lot 19WBA897, Exp. 2020-12-31, GTIN (01)10193489225143.

Where was it sold?

US Nationwide distribution in the states of MN, NE, and PA.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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