CLASS II ONGOING Device recall · Reported 23 Apr 2025 · FDA Enforcement Report

Welch Allyn Green Series 777 Wall System recalled by Baxter Healthcare

Baxter Healthcare is recalling Welch Allyn Green Series 777 Wall System. The recall was initiated on 21 Mar 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes1) Product Code/Part # 77791-2MP2X, UDI/DI 00732094066890; 2) Product Code/Part # 77791-2MP2XL, UDI/DI 00732094201833; 3) Product Code/Part # 77791-2MPX, UDI/DI 00732094066876; 4) Product Code/Part # 77791-2MPX-HS, UDI/DI 00732094231045; 5) Product Code/Part # 77791-2MPXL, UDI/DI 00732094201826; 6) Product Code/Part # 77796-2MPX, UDI/DI 00732094066289; 7) Product Code/Part # 77796-2MPXL, UDI/DI 00732094184013; Lot Number 24-314 & lower

Quantity recalled135 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1566-2025
FDA event ID: 96364
Recalling firm: Baxter Healthcare, Deerfield, IL
Classification: Class II
Status: Ongoing
Recall initiated: 21 Mar 2025
FDA classified: 15 Apr 2025
Reported: 23 Apr 2025
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Labeling Errors
Device type: Other Medical Devices

Timeline

21 Mar 2025	Recall initiated by company
15 Apr 2025	Classified by FDA	+25 days
23 Apr 2025	Published in enforcement report	+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.

Product as listed by the FDA

Welch Allyn Green Series 777 Wall System, Product Code/Part Numbers: 1) 77791-2MP2X; 2) 77791-2MP2XL; 3) 77791-2MPX; 4) 77791-2MPX-HS; 5) 77791-2MPXL; 6) 77796-2MPX; 7) 77796-2MPXL.

Where it was distributed

Worldwide distribution.

Questions about this recall

Why was it recalled?

Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.

Which lots are affected?

1) Product Code/Part # 77791-2MP2X, UDI/DI 00732094066890; 2) Product Code/Part # 77791-2MP2XL, UDI/DI 00732094201833; 3) Product Code/Part # 77791-2MPX, UDI/DI 00732094066876; 4) Product Code/Part # 77791-2MPX-HS, UDI/DI 00732094231045; 5) Product Code/Part # 77791-2MPXL, UDI/DI 00732094201826; 6) Product Code/Part # 77796-2MPX, UDI/DI 00732094066289; 7) Product Code/Part # 77796-2MPXL, UDI/DI 00732094184013; Lot Number 24-314 & lower

Where was it sold?

Worldwide distribution.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

6 other products · FDA event 96364

This product is part of a recall event; the main page for the event is Welch Allyn Connex Vital Signs Monitor recalled by Baxter Healthcare.

Reported	Class	Recall	Company	Reason	Where
23 Apr 2025	CLASS II	Welch Allyn Connex Vital Signs Monitor recalled by Baxter Healthcare	Baxter Healthcare	Labeling Errors	IL
23 Apr 2025	CLASS II	Welch Allyn Welch Allyn Connex Spot Monitor recalled	Baxter Healthcare	Labeling Errors	IL
23 Apr 2025	CLASS II	Welch Allyn DuraShock Aneroid Gauge Sets recalled by Baxter Healthcare	Baxter Healthcare	Labeling Errors	IL
23 Apr 2025	CLASS II	Welch Allyn 2-Piece Reusable Blood Pressure Cuff Kits recalled	Baxter Healthcare	Labeling Errors	IL
23 Apr 2025	CLASS II	Welch Allyn Spot Vital Signs 4400 Device recalled by Baxter Healthcare	Baxter Healthcare	Labeling Errors	IL
23 Apr 2025	CLASS II	Welch Allyn Connex Integrated Wall System recalled by Baxter Healthcare	Baxter Healthcare	Labeling Errors	IL

More recalls from Baxter Healthcare

All 573

Reported	Class	Recall	Company	Reason	Where
16 Sep 2026Drug	CLASS I	Dextrose Injection, USP, 70 % recalled by Baxter Healthcare	Baxter Healthcare	Particulate Matter	Nationwide
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9 Sep 2026Device	CLASS II	Baxter Novum IQ Syringe Pump recalled by Baxter Healthcare	Baxter Healthcare	Device Malfunction	Nationwide
9 Sep 2026Drug	CLASS II	Clindamycin Phosphate in 0.9% Sodium Chloride Injection recalledClindamycin Phosphate	Baxter Healthcare	Manufacturing (CGMP) Deviations	Nationwide

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