The Recall Desk
ModerateFDA (Devices)·Z-1907-2017·Announced 2017-05-10

Breg Inc Recalls Dressing Back P/N 09810 Due to Unsealed Pouches

Breg Inc is recalling 2,609 units of Dressing Back P/N 09810 because approximately 0.22% may have unsealed pouches, rendering them non-sterile.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, which typically corresponds to a moderate severity score when no specific injuries or illnesses are reported in the source text.

Plain-English summary

Breg Inc is recalling 2,609 units of Dressing Back, P/N 09810, distributed nationwide in the United States. These sterile dressings are used as an insulation barrier between the Polar Care cold therapy pad and the skin, typically in post-operative settings.

The recall is due to a determination by Breg that a small percentage (approximately 0.22%) of these products may have been sent with unsealed pouches by the contract manufacturer. Products with unsealed pouches may not have been sealed prior to sterilization and will be non-sterile.

Customers will be contacted and instructed to inspect their inventory for any product with unsealed pouches and discard them.

The recalled product

Product
Dressing Back, P/N 09810 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy pad and the skin. Sterile dressings are typically applied in a non-sterile environment after post-op and on occasion may be applied i
Manufacturer
Breg Inc
Category
Medical Device — Sterile Dressings
Hazard
Affected units
2,609

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 (1)

  • D163404

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 8 recalled by Breg Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 8 products in this recall →

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