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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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High RiskFDA Device
Medical Devices/Surgical Equipment

Stryker Neptune SafeAir Smoke Evacuation Pencils Recalled for Burn Risk

Agency Publication Date: November 13, 2024
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Summary

Stryker Corporation is recalling approximately 3,840,470 Neptune SafeAir Smoke Evacuation Pencils because the devices may activate unintentionally when plugged into a power source or remain active after the buttons are released. This malfunction can cause the device to carry electrical currents through objects or fluids, leading to localized burns for patients and medical staff. The recall includes various coated and non-coated models with rocker-switch and push-button controls. Medical or surgical intervention may be required to treat injuries caused by these unintentional activations.

Risk

The product can activate without manual input or fail to turn off, which may cause localized burns to patients or physicians from electrical currents carried through conductive fluids or objects. If injuries occur, they may require surgical or medical treatment to correct.

What You Should Do

  1. This recall affects multiple models of Stryker Neptune SafeAir Smoke Evacuation Pencils, including coated and non-coated versions with rocker-switch or push-button controls.
  2. Identify your device by checking the catalog number and lot number printed on the product packaging. Affected catalog numbers include 0703-047-000, 0703-047-002, 0703-047-001, 0703-046-000, 0703-046-001, and 0703-046-002. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.
  4. Call the FDA: 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls for additional information.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Stryker Neptune SafeAir Rocker-Switch Smoke Evacuation Pencil, Coated, 70mm
Variants: Coated, 70mm
Model / REF:
0703-047-000
Lot Numbers (183):
53863666
54409859
56319954
56945653
57699375
59053479
65178945
53863667
54409860
56319955
56945654
57699376
59053480
65178946
53863668
54409862
56319956
57699353
57699377
59053481
65178947
53863669
54409919
56319957
57699354
57699378
59053482
65178949
53863670
54409920
56319958
57699355
57699379
59053483
65347997
53863671
54409921
56319959
57699359
57699380
61288937
65784636
54403959
54409922
56319960
57699360
57699381
61288943
65784637
54403960
UDI:
07613327117202

Recall #: Z-0365-2025

Product: Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Rocker-Switch, Bulk Non-Sterile
Variants: Bulk Non-Sterile, Coated, Rocker-Switch
Model / REF:
0703-047-002
Lot Numbers (53):
53700305
53864207
53864241
53864247
60308905
62012084
64112630
65342955
53700306
53864212
53864243
53864248
60308906
62291715
64112631
65869470
53700307
53864213
53864244
53864249
60308907
62291717
64142443
65869471
53700308
53864214
53864245
53864257
61283868
62821201
64968515
65954806
53864205
53864219
53864246
60308904
61283869
64112629
64968516
66005707
53864206
64917537
65342956
66487443
67787272
67840867
68672644
64917538
66487442
67787271
GTIN:
07613327379471

Recall #: Z-0366-2025

Product: Stryker Neptune SafeAir Rocker-Switch Smoke Evacuation Pencil, Non-coated, 70mm
Variants: Non-coated, 70mm
Model / REF:
0703-047-001
Lot Numbers:
64117291
GTIN:
07613327117219

Recall #: Z-0367-2025

Product: Stryker Neptune SafeAir Smoke Evacuation Pencil, Coated, 70mm Blade, Push Button Switch
Variants: Coated, 70mm Blade, Push Button
Model / REF:
0703-046-000
Lot Numbers (204):
54409778
59692168
62016967
63292654
64324200
64855491
65961907
67325428
57699286
60313543
62016978
63292655
64324201
64855498
65961908
67377503
57738329
60313544
62296666
63632847
64324207
64855499
65961909
67481708
57738330
60313545
62296667
63632848
64324208
64855500
66012917
67481709
57738331
60313546
62296668
63632851
64354844
64855501
66012918
67481710
57738332
60313547
62382103
63632852
64354845
64973248
66133412
67481711
57738333
60313549
GTIN:
07613327117202

Recall #: Z-0368-2025

Product: Stryker Neptune SafeAir Smoke Evacuation Pencil, Non-coated, 70mm Blade, Push-Button
Variants: Non-coated, 70mm Blade, Push-Button
Model / REF:
0703-046-001
Lot Numbers:
53867671
54409847
59053476
64855502
66494932
GTIN:
07613327117196

Recall #: Z-0369-2025

Product: Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Push-Button, Bulk Non-sterile
Variants: Bulk Non-sterile, Coated, Push-Button
Model / REF:
0703-046-002
0703
Lot Numbers (61):
53864143
57458172
58761873
63837701
64258041
65777003
66126554
66751061
68311144
54406823
57458173
58761874
63837702
64258042
65777004
66487383
67200500
68311145
54406824
57458174
60308898
63866394
64258044
65954742
66487384
67200501
68672590
54406825
57458175
60308899
63866395
64850548
65954743
66487385
67200502
68728239
54406826
57694644
62291709
64052771
64850549
65954744
66487386
67715714
68728240
54406827
57733684
62377382
64112622
64968511
GTIN:
07613327379488

Recall #: Z-0370-2025

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95502
Status: Active
Manufacturer: Stryker Corporation
Sold By: Authorized Medical Distributors; Hospitals; Surgical Centers
Manufactured In: United States
Units Affected: 6 products (1,120,860 eaches; 295,760 eaches; 2,620 eaches; 1,996,010 eaches; 21,490 eaches; 403,730 eaches)
Distributed To: Nationwide
Agency Last Updated: October 14, 2025

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.