Health product recall

Kretek International Canada Product Recall (2020-10-28)

Starting date:
October 28, 2020
Type of communication:
Drug Recall
Subcategory:
Drugs
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Product Safety
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-74231

Last updated: 2020-10-29

Summary

  • Product: A. DRYFT nicotine pouches 2mg B. DRYFT nicotine pouches 4mg C. DRYFT nicotine pouches 7mg

A. DRYFT nicotine pouches 2mg

B. DRYFT nicotine pouches 4mg

C. DRYFT nicotine pouches 7mg

Reason

Product sold without market authorization (NPN/DIN) in Canada.

Depth of distribution

Retailers

Affected products

DRYFT nicotine pouches 2mg

DIN, NPN, DIN-HIM

No market authorization

Dosage form

Pouch

Strength

2mg nicotine

Lot or serial number

All lots

Companies

Recalling Firm
Kretek International Canada
985 Westport Crescent
Mississauga
L5T 1E8
Ontario
CANADA
Marketing Authorization Holder
N/A

DRYFT nicotine pouches 4mg

DIN, NPN, DIN-HIM

No market authorization

Dosage form

Pouch

Strength

4mg nicotine

Lot or serial number

All lots

Companies

Recalling Firm
Kretek International Canada
985 Westport Crescent
Mississauga
L5T 1E8
Ontario
CANADA
Marketing Authorization Holder
N/A

DRYFT nicotine pouches 7mg

DIN, NPN, DIN-HIM

No market authorization

Dosage form

Pouch

Strength

7mg nicotine

Lot or serial number

All lots

Companies

Recalling Firm
Kretek International Canada
985 Westport Crescent
Mississauga
L5T 1E8
Ontario
CANADA
Marketing Authorization Holder
N/A

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