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Various Endopath Probe Plus II Shafts (April 19, 2013)
- Starting date:
- April 19, 2013
- Posting date:
- April 19, 2013
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Product Safety
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-29243
Reason
Ethicon Endo-Surgery is initiating a recall for Endopath Probe Plus II shafts because of the possibility that a tear in the Tyvek packaging may compromise the sterility of the device which is sold and labeled as Sterile.Us
Affected products
A. Endopath Probe Plus II Shaft-hook Elec.
Lot or serial number
lots with expiry dates between 2015-09 through 2018-03
Model or catalog number
EPS01, EPS05
Companies
- Manufacturer
- Not Applicable
B. Endopath Probe Plus II Shaft-spatula
Lot or serial number
lots with expiry dates between 2015-09 through 2018-03
Model or catalog number
EPS02, EPS06
Companies
- Manufacturer
- Not Applicable
C. Endopath Probe Plus II Shaft-rtangle
Lot or serial number
lots with expiry dates between 2015-09 through 2018-03
Model or catalog number
EPS03, EPS07
Companies
- Manufacturer
- Not Applicable
D. Endopath Probe Plus II Shaft-curved Dis
Lot or serial number
lots with expiry dates between 2015-09 through 2018-03
Model or catalog number
EPS04, EPS08
Companies
- Manufacturer
- Not Applicable
E. Endopath Probe Plus II Shaft-irrigation
Lot or serial number
lots with expiry dates between 2013-04 through 2018-03
Model or catalog number
EPS10, EPS11
Companies
- Manufacturer
- Not Applicable
F. Endopath Probe Plus II Shaft-stone Ret.
Lot or serial number
lots with expiry dates between 2013-04 through 2018-03
Model or catalog number
EPS12
Companies
- Manufacturer
- Not Applicable
G. Endopath Probe Plus II Shaft-flex Fibre
Lot or serial number
lots with expiry dates between 2013-04 through 2018-03
Model or catalog number
EPS13
Companies
- Manufacturer
- Not Applicable
- Date modified: