510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-1298-2017Class II

Eye Plastic Tray, part number PSS1931(A

Windstone Medical Packaging, Inc. / initiated 2017-01-11 / Terminated / root cause: manufacturing process

Windstone Medical Packaging, Inc. began a recall of Eye Plastic Tray, part number PSS1931(A on . FDA classified it as Class II and gives the reason as "The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility". As of , the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number
Z-1298-2017
Classification
Class II
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Windstone Medical Packaging, Inc.
Product
Eye Plastic Tray, part number PSS1931(A
Product code
FSY Light, Surgical, Ceiling Mounted
Reason for recall
The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.
Root cause tag
manufacturing process
FDA root cause
Nonconforming Material/Component
Action
AMS notified their consignees by Email, Fax, and Phone on 11/11/2017. AMS sent the notification letter, dated January 11, 2017, and provided yellow stickers "Recall Notice" to customers. They are advised to over-label the affected AMS kits at their facilities. Customers were instructed to place sticker in such a way that it would be immediately noticed but should not cover up or conceal any pertinent information such as Pack Number, Pack Name, Lot Number or Expiration Date on a kit. Customers with questions can call Vicki Davis at 321-527-7714 or send email to [email protected].
Quantity in commerce
310 kits
Distribution
Distributed in AZ, CA, CO, CT, FL, GA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NV, OH, PA, TX, UT, VA, and WA.
Product codes and lots
Lot number and expiration date  84566, 3/8/2017 85861, 7/5/2017 86513, 8/27/2017 88308, 11/30/2017 88550, 11/12/2017 88986, 11/1/2017 96822, 2/17/2018 97615, 2/5/2018 97993, 7/9/2018

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-1298-2017
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-1258-2017Class IITerminatedVoluntary: Firm initiated
Z-1259-2017Class IITerminatedVoluntary: Firm initiated
Z-1260-2017Class IITerminatedVoluntary: Firm initiated
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Z-1266-2017Class IITerminatedVoluntary: Firm initiated
Z-1267-2017Class IITerminatedVoluntary: Firm initiated
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Z-1270-2017Class IITerminatedVoluntary: Firm initiated
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Z-1364-2017Class IITerminatedVoluntary: Firm initiated
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Z-1366-2017Class IITerminatedVoluntary: Firm initiated
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