FDA recall, , Moderate risk
Pilling Wecksorb Neurosponges and Neurosponge Strips
Pilling Wecksorb Neurosponges and Neurosponge Strips may have out-of-specification levels of endotoxins.
Summary by Recall Canary from the FDA notice
What happened
Teleflex LLC of Morrisville, North Carolina, recalled Pilling Wecksorb Neurosponges (Cotton) and Pilling Wecksorb Neurosponge Strips (Cotton) due to out-of-specification, or potential out-of-specification, levels of endotoxins. The recall began May 7, 2026, and was added to the FDA's Enforcement Report on July 1, 2026. Distribution included nationwide in the United States and the country of Panama.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the lot code and model/catalog number or model number listed under your product.
Incomplete list: 40 of 172 lot codes shown.
Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips (Cotton)
- Model/Catalog number
- 200100 200101 200102 200103 200104 200105 200106 200108 200110 200112 200120 200121 200123 200131
- Lot code
- 21E1485
- 21H2304
- 21H2594
- 21H2595
- 21K3161
- 21L3593
- 22A0175
- 22C0661
- 22E1386
- 22J2777
- 22K3102
- 22K3269
- 22K3270
- 23A0102
- 23D0796
- 23D0900
- 23E1180
- 23H1834
- 24C0647
- 24E1133
- 24G1865
- 24G1864
- 24K2820
- 21E1503
- 21E1546
- 21H2596
- 21K3162
- 21L3594
- 22B0456
- 22C0677
- 22D1299
- 22K3271
- 23A0103
- 23E1235
- 23H1835
- 24G1863
- 24H2070
- 24K2821
- 21E1397
- 21E1547
- Recall number
- Z-2639-2026
- Model number
- 200100
- 200101
- 200102
- 200103
- 200104
- 200105
- 200106
- 200108
- 200110
- 200112
- 200120
- 200121
- 200123
- 200131
Recall details
- Company began the recall
- Sold in
Worldwide - U.S. Nationwide distribution including in the states of Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, and West Virginia. The country of Panama.
- Company
- TELEFLEX LLCMorrisville, North Carolina
- Hazard
- Quality testing problem
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98962
- Recall number
- Z-2639-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
