CLASS II ONGOING Device recall · Reported 13 Dec 2023 · FDA Enforcement Report

Remington Medical Drainage Bag, REF 600-D recalled

Remington Medical is recalling Remington Medical Drainage Bag, REF 600-D, distributed in Florida, Pennsylvania. The recall was initiated on 3 Nov 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUDI/DI 20813079020008, Lot Number 2325111

Quantity recalled3080 devices

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-0487-2024
FDA event ID: 93377
Recalling firm: Remington Medical, Alpharetta, GA
Classification: Class II
Status: Ongoing
Recall initiated: 3 Nov 2023
FDA classified: 5 Dec 2023
Reported: 13 Dec 2023
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

3 Nov 2023	Recall initiated by company
5 Dec 2023	Classified by FDA	+32 days
13 Dec 2023	Published in enforcement report	+8 days

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

Reason for recall

There is an error with the "Use by Date" and "Date of Manufacturer" on the box label.

Product as listed by the FDA

Remington MEDICAL Drainage Bag, REF 600-D;

Where it was distributed

US: PA and FL

Florida Pennsylvania

Questions about this recall

Why was it recalled?

There is an error with the "Use by Date" and "Date of Manufacturer" on the box label.

Which lots are affected?

UDI/DI 20813079020008, Lot Number 2325111

Where was it sold?

US: PA and FL

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

More recalls from Remington Medical

All 4

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4 Jan 2023Device	CLASS II	Automatic Cutting Needle recalled by Remington Medical	Remington Medical	Other	6 states
16 Apr 2014Device	CLASS II	Fas-loc 6 Foot Disposable Extension Cable recalled by Remington Medical	Remington Medical	Other	Nationwide
17 Oct 2012Device	CLASS II	Automatic Cutting Needles, Soft Tissue Biopsy Needle recalled	Remington Medical	Sterility	Nationwide

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