Reported May 10, 2017 · Terminated
11.0cm Long Attachment Product Usage: Pneumatic system
The Anspach Effort, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: The Anspach Effort, Inc. · 4500 Riverside Dr · Palm Beach Gardens, FL · 33410-4235
Is this the product you have?
- 11.0cm
- Long Attachment Product UsagePneumatic system
- Lot codes and dates
- All serial numbers shipped to customers prior to 09/27/2016; DFU 18-0048; Part No. LONG.
- Amount recalled
- 3504
This recall covers 103 products
The agency filed one notice per product. You are reading one of them; the other 102 are below.
90 more are in the archive.
Where it was sold
Why it was recalled
Supplied Directions for Use (DFU) did not contain a recommended service interval.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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