The Recall Desk
Agency classClass IIOur severity:SevereFDA (Drugs)·D-0397-2018·Announced 2018-02-21

Sage Products Recalls Q.Care Oral Cleansing Systems Due to Cross-Contamination

Sage Products Inc. is recalling Q.Care Oral Cleansing & Suctioning Systems because oral care solutions were manufactured on equipment shared with non-pharmaceutical products.

The agency’s classification

FDA (Drugs): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The FDA classified this as a Class II recall. Per the rubric, FDA Class II recalls are assigned a severity score of 4 (Severe), particularly when involving potential contamination risks in medical devices.

Plain-English summary

Sage Products Inc. is recalling 2,468 cases of the Q.Care Oral Cleansing & Suctioning System q8. The product includes a covered Yankauer suction handle, suction toothbrushes with antiseptic solution, suction oral swabs with Perox-A-Mint solution, and an oropharyngeal suction catheter. The affected lots are 57592, 58202, 59213, 60274, 60718, and 61745, with expiration dates ranging from August 14, 2017, to March 21, 2018.

The recall was initiated because the oral care solutions were manufactured by a third-party supplier on equipment that was shared with non-pharmaceutical products, creating a risk of cross-contamination. The FDA has classified this as a Class II recall, indicating a reasonable probability that use of the product could cause temporary or medically reversible adverse health consequences.

The affected products were distributed nationwide in the United States and Puerto Rico, as well as in Canada, the United Kingdom, Ireland, the Netherlands, and New Zealand. Consumers and healthcare facilities should stop using the affected products and contact Sage Products Inc. for instructions on return or disposal.

The recalled product

Product
Q.Care Oral Cleansing & Suctioning System q8. Contains 1 Covered Yankauer Suction Handle and Y-Connector, 2 Suction Toothbrush packages with Antiseptic Solution,, 1 Suction Oral Swab packages with Perox-A-Mint solution, 1 Oropharyngeal Suction Catheter package. Sage Products…
Manufacturer
Sage Products Inc
Category
Medical Device — Oral Care / Suctioning
Hazard
Affected units
2,468

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (12)

  • Product Code: 6808
  • Lots: 57592
  • EXP 08/14/2017
  • 58202
  • EXP 10/02/2017
  • 59213
  • EXP 11/13/2017
  • 60274
  • EXP 01/02/2018
  • 60718 EXP 02/05/2018
  • 61745
  • EXP 03/21/2018.

Distribution

Distributed nationwide across the United States.

The notice also names 1 state specifically:

Part of a larger recall action

This product is one of 64 recalled by Sage Products Inc under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 64 products in this recall →

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