Cambridge Baby Crib Recall [Canada]


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Canada/Ottawa: Cambridge Baby Crib Recall [Canada]Benjamin Strollers recalls an estimated 102 Cambridge Baby Cribs due to entrapment and/or laceration hazards. HCSC: http://ht.ly/L4V4305CeZv

Direct link: http://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2016/60614r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports this recall involves certain Cambridge Baby Cribs with a manufacturing date of December 25, 2015 and model number CAM-CR-WH1. The affected Cribs are white in colour and can be converted into a bed.

Please consult the photograph above for details of the product’s packaging, design and retail presentation.

According to Health Canada, its sampling and evaluation program has determined that these Cribs do not meet the Cribs, Cradles and Bassinets Regulations in Canada. Specifically, the mattress support system of the recalled Cribs can break, creating an uneven sleeping surface and/or a gap. If this defect occurs, a child can become entrapped in the Crib, fall or be cut by the broken metal.

Neither Health Canada nor Benjamin Strollers has received any reports of consumer incidents or injuries related to the use of these Cribs in Canada.

If you believe you have purchased or have in your possession any of the recalled Cambridge Baby Cribs, please do not use them for your child. Instead, kindly contact Benjamin Strollers to obtain a replacement mattress support. In the meantime, parents and other caregivers should find an alternate safe sleeping environment for the child. Please consult Heath Canada’s Web page here:

Is Your Child Safe? Sleep Time:
http://www.hc-sc.gc.ca/cps-spc/pubs/cons/child-enfant/sleep-coucher-eng.php

If you have any questions about this recall notification, please contact Benjamin Strollers at 1-647-930-3578.

Please note: the Canada Consumer Product Safety Act prohibits recalled products from being redistributed, sold or even given away in Canada.

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Additional information about this recall:
HCSC ID number: RA-60614
Recalls Direct RIN: 7787-2016
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