CLASS II ONGOING Device recall · Reported 30 Apr 2014 · FDA Enforcement Report

Nice-En-Smooth Berry Burst recalled by Altasource

Altasource is recalling Nice-En-Smooth Berry Burst, distributed nationwide in the US. The recall was initiated on 3 Feb 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 8-94034

Quantity recalled42

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-1500-2014
FDA event ID: 67976
Recalling firm: Altasource, Roswell, GA
Classification: Class II
Status: Ongoing
Recall initiated: 3 Feb 2014
FDA classified: 24 Apr 2014
Reported: 30 Apr 2014
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

3 Feb 2014	Recall initiated by company
24 Apr 2014	Classified by FDA	+80 days
30 Apr 2014	Published in enforcement report	+6 days

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

Reason for recall

Firm is not registered as a drug manufacturer.

Product as listed by the FDA

Nice-En-Smooth Berry Burst, 4 oz., Manufactured by Meta Labs LLC, UPC 80604-8 Product Usage: Flavored lubricant water based, condom friendly jelly used to enhance or replace a womans natural lubrication.

Where it was distributed

USA Nationwide in the states of AZ, AR, CA, CO, FL, GA, ID, IL,KY, LA, MI, NE, NV, NY, NC, OH, PA, TN, TX, UT, and VA.

Nationwide Arkansas Arizona California Colorado Florida Georgia Idaho Illinois Kentucky Louisiana Michigan North Carolina Nebraska Nevada New York Ohio Pennsylvania Tennessee Texas Utah

Questions about this recall

Is Nice-En-Smooth Berry Burst recalled?

Yes. Altasource recalled Nice-En-Smooth Berry Burst on 3 Feb 2014. The recall is Class II and its status is Ongoing. Recall number Z-1500-2014.

Why was it recalled?

Firm is not registered as a drug manufacturer.

Which lots are affected?

Lot 8-94034

Where was it sold?

USA Nationwide in the states of AZ, AR, CA, CO, FL, GA, ID, IL,KY, LA, MI, NE, NV, NY, NC, OH, PA, TN, TX, UT, and VA.

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.

More recalls from Altasource

All 4

Reported	Class	Recall	Company	Reason	Where
30 Apr 2014Device	CLASS II	Mega-Gen His Personal Lubricant, Meta Labs recalled by Altasource	Altasource	Other	Nationwide
30 Apr 2014Device	CLASS II	Amo-O Herbal Stimulator recalled by Altasource	Altasource	Other	Nationwide
30 Apr 2014Device	CLASS II	Hot Ice, Meta Labs LLC recalled by Altasource	Altasource	Other	Nationwide

Other Other Medical Devices recalls

All 13,778

Reported	Class	Recall	Company	Reason	Where
16 Sep 2026Device	CLASS II	Citric Complete Dry Citric Acid Concentrate recalled	Nipro Renal Soultions USA	Other	Nationwide
16 Sep 2026Device	CLASS I	Kit: Epidural/Pain TQC 20/Cs recalled by Medical Action Industries	Medical Action Industries Inc. 306	Sterility	6 states
16 Sep 2026Device	CLASS II	Halyard IV Start Kit Non-Sterile recalled by Avid Medical	Avid Medical	Sterility	Nationwide
16 Sep 2026Device	CLASS I	Kit: Single Shot Epidural 20/Cs recalled by Medical Action Industries	Medical Action Industries Inc. 306	Sterility	6 states
16 Sep 2026Device	CLASS II	AMS Convenience Kit: Dsaek Pack - RX recalled	Windstone Medical Packaging	Device Malfunction	Nationwide