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FDA (Drug enforcement)Recalled 2014-10-17closedclass ii

Obagi Medical Products: Obagi Nu-Derm Clear, AM PM 3, Skin Bleaching and Corrector Cream, Hydroquinone USP, 4%, Rx Only, Net Wt. 2 OZ. (57 g) bottle, Dist by OMP Inc, Long Beach CA 90802, Made in USA,

Is my product affected?

Obagi Nu-Derm Clear, AM PM 3, Skin Bleaching and Corrector Cream, Hydroquinone USP, 4%, Rx Only, Net Wt. 2 OZ. (57 g) bottle, Dist by OMP Inc, Long Beach CA 90802, Made in USA, NDC 62032-101-36

  • Brand OBAGI NU-DERM SYSTEM NORMAL-OILY SKIN TRANSFORMATION
  • UPC 362032101361

Check against the official notice below — it lists the full affected range.

What happened

Obagi Medical Products has recalled 975 bottles of Obagi Nu-Derm Clear due to a label mix-up. Pre-labeled bottles of Obagi Nu-Derm Clear were accidentally placed into the Obagi Exfoderm Forte packaging line, meaning customers who ordered Clear RX received bottles labeled as Clear but containing Exfoderm Forte instead. The affected product is a hydroquinone 4% cream distributed nationwide as well as in Mexico and Slovenia, with lot number 13I1218, product number 362032101361, and an expiration date of 09/30/2016.

The recall affects bottles with the specific lot and product numbers listed above. The source document does not specify what consumers should do in response to this recall.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Labeling: Label Mix-Up; Containers of the Obagi Nu-Derm Clear pre-labeled bottles were inadvertently introduced into the Obagi Exfoderm Forte packaging line. Therefore customers which ordered Clear RX actually had contents of Exfoderm forte.

Details from the source

Reason for recall: Labeling: Label Mix-Up; Containers of the Obagi Nu-Derm Clear pre-labeled bottles were inadvertently introduced into the Obagi Exfoderm Forte packaging line. Therefore customers which ordered Clear RX actually had contents of Exfoderm forte. Distribution: Nationwide and Mexico and Slovenia Quantity: 975 bottles Lot/code info: Lot #: 13I1218, Product/Part #: 362032101361, Exp 09/30/2016

Source

Official record: FDA (Drug enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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