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-1280-2017Class II

Catheter Pack, part number AMS4399(A

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

Windstone Medical Packaging, Inc. began a recall of Catheter Pack, part number AMS4399(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-1280-2017
Classification
Class II
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Windstone Medical Packaging, Inc.
Product
Catheter Pack, part number AMS4399(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
1116 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  84598 4/16/2017 84599 5/8/2018 85277 5/11/2018 85342 5/17/2018 85456 6/3/2018 85629 6/11/2018 85630 8/21/2018 87145 10/15/2018 89443 8/23/2018 89892 11/30/2018 95180 8/24/2018 95298 11/21/2018 95789 11/11/2018 96424 12/26/2018 96494 12/17/2018 96945 3/11/2019 97753 4/3/2019 97817 4/12/2019 98124 4/18/2019 98703 5/23/2019 98704 6/7/2019 98940 6/30/2019 99561 6/17/2019 99900 6/29/2019

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-1280-2017
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-1258-2017Class IITerminatedVoluntary: Firm initiated
Z-1259-2017Class IITerminatedVoluntary: Firm initiated
Z-1260-2017Class IITerminatedVoluntary: Firm initiated
Z-1261-2017Class IITerminatedVoluntary: Firm initiated
Z-1262-2017Class IITerminatedVoluntary: Firm initiated
Z-1263-2017Class IITerminatedVoluntary: Firm initiated
Z-1264-2017Class IITerminatedVoluntary: Firm initiated
Z-1265-2017Class IITerminatedVoluntary: Firm initiated
Z-1266-2017Class IITerminatedVoluntary: Firm initiated
Z-1267-2017Class IITerminatedVoluntary: Firm initiated
Z-1268-2017Class IITerminatedVoluntary: Firm initiated
Z-1269-2017Class IITerminatedVoluntary: Firm initiated
Z-1270-2017Class IITerminatedVoluntary: Firm initiated
Z-1271-2017Class 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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