SBS - The best value in QMS software

Eliminating Mislabeled Product

Cari Spears

Super Moderator
Staff member
Super Moderator
#11
Dana Stout said:
...the operator then checks to ensure they were given the proper labels. ... The only reason I can find for mislabels at my company is operator's not following procedures.
(My bold in the quote above.) So - the operator has to have been given the incorrect label then. I do not think that operators not following procedures is your root cause - they might not catch the error - but the function providing them the labels is where I would direct my investigation.

Who gives the operator the label and how is it possible for them to give the operator the wrong label?
 
Elsmar Forum Sponsor

Al Rosen

Staff member
Super Moderator
#12
Cari Spears said:
(My bold in the quote above.) So - the operator has to have been given the incorrect label then. I do not think that operators not following procedures is your root cause - they might not catch the error - but the function providing them the labels is where I would direct my investigation.

Who gives the operator the label and how is it possible for them to give the operator the wrong label?
Exactly!
 

qcman

Registered Visitor
#13
Believe me you are not the only one with miss labeling issues.When I came on it was one of the more up front problems not only to the customer but between departments.Compounding the problem here was that part *A* went to machine #2 as one piece/number and left as 2 different part numbers ( a left and right hand).Not only were they miss labeling them but were mixing the loads also.I put flag pole signs on each lay aside cart with the part number on each.Once done they moved to a staging area where a board was put up with certified part samples where the supervisor of that department had to physically verify the correct part/ label with the sample and sign off the move ticket on each box before it could move to the next department.Once finished in that department the parts again were verified using another sample board and a orange dot placed on the box by supervision before it was allowed to be taken to shipping.Once in shipping the clerk enters the information into the computer which creates the label then he is the one who puts the label on. Once labeled each box is scanned and the supervisor downloads the scan info which if not correct the main frame will alert him of a problem.This type of system may not work for you but the general idea is to have multiple verification points in the system.It still happens now and then but it has eliminated most of the problem for us.
 

Miner

Forum Moderator
Staff member
Admin
#14
We had a similar weldment process compounded with RH/LH product. We implemented the Best Practices document I provided earlier, color-coded all paperwork, and added pictures of the product that highlighted unique features.

The final improvement that completely eliminated the errors was to add a bar code to the part specific documentation. The operator scanned this barcode and a printer next to the pallet printed the exact quantity of labels needed to label the pallet.
 

Al Rosen

Staff member
Super Moderator
#15
Miner said:
We had a similar weldment process compounded with RH/LH product. We implemented the Best Practices document I provided earlier, color-coded all paperwork, and added pictures of the product that highlighted unique features.

The final improvement that completely eliminated the errors was to add a bar code to the part specific documentation. The operator scanned this barcode and a printer next to the pallet printed the exact quantity of labels needed to label the pallet.
That's a beutiful thing! Beats all non value added inspections.
 
Thread starter Similar threads Forum Replies Date
M Medical Device News FDA - Eliminating Routine FDA news 14-09-18 - Re-Review of Third Party 510(k) Reviews Other US Medical Device Regulations 0
M Methods of reducing/eliminating the systematic component of error General Measurement Device and Calibration Topics 0
W Eliminating Paperwork using Inspection Stamps AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
J Eliminating Missing Steps In Manual Operations Human Factors and Ergonomics in Engineering 8
T Eliminating "Hard Copy" Manuals from our Office and Shop Floor - Documentation Medium ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
E Wiki vs. Controlled Documents - Eliminating Conflicts Quality Manager and Management Related Issues 5
W Authorizing Product Release while Eliminating In-Process Inspection Records ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
W Eliminating an Army of Inspectors - Batch Manufacturer Philosophy, Gurus, Innovation and Evolution 12
R Eliminating Cosmetic Issues and Customer Complaints Problem Solving, Root Cause Fault and Failure Analysis 14
L Eliminating a Recurring Problem of Missing Weld Nuts/Fasteners Manufacturing and Related Processes 27
P Quality Operating Procedures - Eliminating the term 'Quality' Document Control Systems, Procedures, Forms and Templates 34
T TS 16949 is a way of Eliminating each of your Customers Auditing you - Need to Vent IATF 16949 - Automotive Quality Systems Standard 40
P Eliminating Systemic Errors in the Labeling Process Manufacturing and Related Processes 21
C Eliminating seven wastes - How do I and what are some good information resources? Quality Tools, Improvement and Analysis 5
P Lean Manufacturing - Eliminating Inspection - Can Quality Survive? Lean in Manufacturing and Service Industries 49
J Hardcopy vs. Electronic Training Records - Eliminating Hardcopy Records Records and Data - Quality, Legal and Other Evidence 13
D GMP Inspection Requirements - Eliminating Visual status of finished goods Inspection, Prints (Drawings), Testing, Sampling and Related Topics 6
D Supplier Eliminating Inspection because it is not Economically Feasible Supplier Quality Assurance and other Supplier Issues 5
J Part Approval - Eliminating Incoming Quality Inspection by Customer Inspection, Prints (Drawings), Testing, Sampling and Related Topics 4
M Corrective Action - Customer Received Mislabeled Parts Nonconformance and Corrective Action 6
M Label Error Proofing - Mislabeled parts in a small automotive company Manufacturing and Related Processes 25
A Migrating from whole product CE marking to modular approach CE Marking (Conformité Européene) / CB Scheme 1
H Medical device Product Registration Registrars and Notified Bodies 2
A Can a power Supply be an accessory to a medical device, if it is an 'off-the-shelf' product. IEC 60601 - Medical Electrical Equipment Safety Standards Series 3
M Extension to shelf life of new product under MDR EU Medical Device Regulations 1
lanley liao Are there guidelines for application of all API monogrammal product? Oil and Gas Industry Standards and Regulations 2
S ISO 11137- Simulated product vs SIP Other Medical Device Related Standards 2
K "World Class Product" based QM. I need advice. Quality Management System (QMS) Manuals 14
R IATF 16949 Certification for new site with transferred product--what is the impact with CSR and scorecards? IATF 16949 - Automotive Quality Systems Standard 0
William55401 Distributed By Product - Best Practices for Configuration Management and Purchasing Controls ISO 13485:2016 - Medical Device Quality Management Systems 0
R Compatibility studies - combination product CE Marking (Conformité Européene) / CB Scheme 4
R Compatibility studies - Medicinal Product and Medical Device Other ISO and International Standards and European Regulations 0
J Marking "Distributed By" to product with distributors' reference-code EU Medical Device Regulations 3
dinaroxentool Selling a product in Both UK and EU after Brexit UK Medical Device Regulations 9
P EU MDR Translation of Product Name EU Medical Device Regulations 1
N Is this a single integral drug device combination product EU MDR CE Marking (Conformité Européene) / CB Scheme 1
V New Product Model CE Mark Certification under MDR EU Medical Device Regulations 0
Sidney Vianna Informational APQP4Wind - Advanced Product Quality Planning for the Wind Power Supply Chain APQP and PPAP 3
K 510k FDA review, will they accept Biocompatibility result generated using feasibility product lots? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 8
G Adopting old product - compliance with IEC 62304 IEC 62304 - Medical Device Software Life Cycle Processes 9
S How long does it take to register a product with MHRA? UK Medical Device Regulations 4
D Classification of product for clinical trials EU Medical Device Regulations 14
N Adding unclassified product to the medical device registration US Food and Drug Administration (FDA) 1
B Internal Auditor Competency - Product Auditors Internal Auditing 9
T PFMEA and Control Plans on legacy product FMEA and Control Plans 5
P FDA Approved Product Contact Parts ISO 13485:2016 - Medical Device Quality Management Systems 6
S AS9120B - 8.5.2 Delivering Split Product AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
S Classification of a product according to MDR EU Medical Device Regulations 3
optomist1 Informational Training IMDS - Management of Product Chemical Regulatory Compliance RoHS, REACH, ELV, IMDS and Restricted Substances 2
L AS9100 - Product and Service Provision 8.5.1q AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6

Similar threads

Top Bottom