CLASS II ONGOING Device recall · Reported 11 Oct 2023 · FDA Enforcement Report

Puritan Bennett Cuff Pressure Manager recalled by Covidien

Covidien is recalling Puritan Bennett Cuff Pressure Manager, distributed in 16 states. The recall was initiated on 22 Aug 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUDI-DI: 10884521782495, Serial Numbers: E223500003, E223500004, E223500005, E223500006, E223500007, E223500008, E223500009, E223500010, E223500011, E223500012, E223500013, E223500014, E223500015, E223500016, E223500017, E223500018, E223500019, E223500020, E223500021, E223500022, E223500023, E223500024, E223500025, E223500026, E223500027, E223500028, E223500029, E223500030, E223500031, E223500032, E223500054, E223500055, E223500079, E223500080, E223500081, E223500082, E223500083, E223600009, E223600010, E223600011, E223600012, E223600013, E223600014, E223600015, E223600016, E223600017, E223600018, E223600019, E223600020, E223600021, E223600022, E223600023, E223600024, E223600042, E223600070, E223600071, E223600072, E223600073, E223600074, E223600075, E223600076, E223600077, E223600078, E223600079, E223600080, E223600081, E223600082, E223600083, E223600084, E223600085, E223600086, E223600087, E223600088, E223600089, E223600090, E223600092, E223600093, E223600095, E223600096, E223600097, E223600098, E223600099, E223600100, E224900001, E224900002, E224900003, E224900004, E224900005, E224900006, E224900007, E224900008, E224900009, E224900010, E224900011, E224900012, E224900013, E224900014, E224900015, E224900017, E224900018, E224900019, E224900020, E224900021, E224900022, E224900023, E224900024, E224900025, E224900026, E224900027, E224900028, E224900029, E224900030, E224900031, E224900032, E224900033, E224900034, E224900035, E224900036, E224900037, E224900039, E224900040, E224900041, E224900042, E224900043, E224900044, E224900045, E224900047, E224900048, E224900049, E224900050, E224900052, E224900053, E224900055, E224900056, E224900057, E224900058, E224900059, E224900060, E224900061, E224900062, E224900064, E224900065, E224900066, E224900067, E224900068, E224900069, E224900070, E224900072, E224900073, E224900074, E224900075, E224900076, E224900077, E224900078, E224900081, E224900082, E224900083, E224900084, E224900085, E224900087, E224900091, E224900092, E224900093, E224900094, E224900095, E224900098, E224900099, E224900100, E225000001, E225000002, E225000003, E225000004, E225000005, E225000006, E225000007, E225000011, E225000012, E225000013, E225000014, E225000015, E225000016, E225000017, E225000018, E225000019, E225000020, E225000021, E225000022, E225000023, E225000024, E225000025, E225000026, E225000027, E225000029, E225000031, E225000032, E225000033, E225000034, E225000035, E225000036, E225000037, E225000038, E225000039, E225000040, E225000041, E225000042, E225000043, E225000044, E225000045, E225000046, E225000047, E225000048, E225000049, E225000050, E225000051, E225000052, E225000053, E225000054, E225000055, E225000056, E225000057, E225000058, E225000059, E225000060, E225000061, E225000062, E225000063, E225000064, E225000065, E225000066, E225000067, E225000068, E225000069, E225000070, E225000071, E225000072, E225000073, E225000075, E225000076, E225000077, E225000078, E225000079, E225000080, E225000081, E225000082, E225000083, E225000084, E225000085, E225000086, E225000087, E225000088, E225000089, E225000090, E225000091, E225000092, E225000093, E225000094, E225000095, E225000096, E225000097, E225000098, E225000099, E225000100, E230200001, E230200002, E230200003, E230200004, E230200005, E230200006, E230200007, E230200008, E230200009, E230200010, E230200011, E230200012, E230200013, E230200014, E230200015, E230200016, E230200017, E230200018, E230200019, E230200020, E230200021, E230200022, E230200023, E230200024, E230200025, E230200027, E230200028, E230200029, E230200030, E230200031, E230200032, E230200033, E230200034, E230200035, E230200036, E230200037, E230200038, E230200039, E230200040, E230200041, E230200042, E230200043, E230200044, E230200045, E230200046, E230200048, E230200049, E230200050, E230200051, E230200052, E230200053, E230200054, E230200056, E230200057, E230200058, E230200059, E230200060, E230200061, E230200062, E230200064, E230200065, E230200066, E230200067, E230200068, E230200069, E230200070, E230200071, E230200072, E230200073, E230200074, E230200075, E230200076, E230200077, E230200078, E230200079, E230200080, E230200081, E230200082, E230200083, E230200085, E230200086, E230200087, E230200088, E230200089, E230200090, E230200091, E230200092, E230200095, E230200096, E230500006, E230500007, E230500008, E230500009, E230500010, E230500011, E230500031, E230500032, E230500033, E230500034, E230500035, E230500036, E230500037, E230500038, E230500039, E230500040, E230500041, E230500042, E230500043, E230500044, E230500045, E230500046, E230500047, E230500048, E230500049, E230500050, E230500051, E230500052, E230500053, E230500054, E230500055, E230500056, E230500057, E230500058, E230500059, E230500060, E230500061, E230500062, E230500063, E230500064, E230500065, E230500066, E230500092, E230500093, E230500094, E230500103, E230500104, E230500105, E230500106, E230500107, E230500108, E230500109, E230500110, E230500111, E230500112, E230900079, E230900080

Quantity recalled408

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-2651-2023
FDA event ID: 92941
Recalling firm: Covidien, Boulder, CO
Classification: Class II
Status: Ongoing
Recall initiated: 22 Aug 2023
FDA classified: 29 Sep 2023
Reported: 11 Oct 2023
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Lead & Heavy Metals
Device type: Other Medical Devices

Timeline

22 Aug 2023	Recall initiated by company
29 Sep 2023	Classified by FDA	+38 days
11 Oct 2023	Published in enforcement report	+12 days

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

Reason for recall

Inadequate internal fixation of the power inlet port to the cuff pressure manager device causes the external power inlet to became dislodged within the device housing after several uses, which prevents the device from being charged, and could lead to treatment delay.

Lead and other heavy metals accumulate in the body. Children are most at risk; even low levels can affect development.

Product as listed by the FDA

Puritan Bennett Cuff Pressure Manager, REF: 180-03

Where it was distributed

US: AL, NJ, MA, MI, NY, NC, CO, TX, FL, KY, UT, CA, AZ, KS, IL, TN. OUS: El Salvador, Sweden, Canary Islands

Alabama Arizona California Colorado Florida Illinois Kansas Kentucky Massachusetts Michigan North Carolina New Jersey New York Tennessee Texas Utah

Stores named: Walmart

Questions about this recall

Is Puritan Bennett Cuff Pressure Manager recalled?

Yes. Covidien recalled Puritan Bennett Cuff Pressure Manager on 22 Aug 2023. The recall is Class II and its status is Ongoing. Recall number Z-2651-2023.

Why was it recalled?

Which lots are affected?

UDI-DI: 10884521782495, Serial Numbers: E223500003, E223500004, E223500005, E223500006, E223500007, E223500008, E223500009, E223500010, E223500011, E223500012, E223500013, E223500014, E223500015, E223500016, E223500017, E223500018, E223500019, E223500020, E223500021, E223500022, E223500023, E223500024, E223500025, E223500026, E223500027, E223500028, E223500029, E223500030, E223500031, E223500032, E223500054, E223500055, E223500079, E223500080, E223500081, E223500082, E223500083, E223600009, E223600010, E223600011, E223600012, E223600013, E223600014, E223600015, E223600016, E223600017, E223600018, E223600019, E223600020, E223600021, E223600022, E223600023, E223600024, E223600042, E223600070, E223600071, E223600072, E223600073, E223600074, E223600075, E223600076, E223600077, E223600078, E223600079, E223600080, E223600081, E223600082, E223600083, E223600084, E223600085, E223600086, E223600087, E223600088, E223600089, E223600090, E223600092, E223600093, E223600095, E223600096, E223600097, E223600098, E223600099, E223600100, E224900001, E224900002, E224900003, E224900004, E224900005, E224900006, E224900007, E224900008, E224900009, E224900010, E224900011, E224900012, E224900013, E224900014, E224900015, E224900017, E224900018, E224900019, E224900020, E224900021, E224900022, E224900023, E224900024, E224900025, E224900026, E224900027, E224900028, E224900029, E224900030, E224900031, E224900032, E224900033, E224900034, E224900035, E224900036, E224900037, E224900039, E224900040, E224900041, E224900042, E224900043, E224900044, E224900045, E224900047, E224900048, E224900049, E224900050, E224900052, E224900053, E224900055, E224900056, E224900057, E224900058, E224900059, E224900060, E224900061, E224900062, E224900064, E224900065, E224900066, E224900067, E224900068, E224900069, E224900070, E224900072, E224900073, E224900074, E224900075, E224900076, E224900077, E224900078, E224900081, E224900082, E224900083, E224900084, E224900085, E224900087, E224900091, E224900092, E224900093, E224900094, E224900095, E224900098, E224900099, E224900100, E225000001, E225000002, E225000003, E225000004, E225000005, E225000006, E225000007, E225000011, E225000012, E225000013, E225000014, E225000015, E225000016, E225000017, E225000018, E225000019, E225000020, E225000021, E225000022, E225000023, E225000024, E225000025, E225000026, E225000027, E225000029, E225000031, E225000032, E225000033, E225000034, E225000035, E225000036, E225000037, E225000038, E225000039, E225000040, E225000041, E225000042, E225000043, E225000044, E225000045, E225000046, E225000047, E225000048, E225000049, E225000050, E225000051, E225000052, E225000053, E225000054, E225000055, E225000056, E225000057, E225000058, E225000059, E225000060, E225000061, E225000062, E225000063, E225000064, E225000065, E225000066, E225000067, E225000068, E225000069, E225000070, E225000071, E225000072, E225000073, E225000075, E225000076, E225000077, E225000078, E225000079, E225000080, E225000081, E225000082, E225000083, E225000084, E225000085, E225000086, E225000087, E225000088, E225000089, E225000090, E225000091, E225000092, E225000093, E225000094, E225000095, E225000096, E225000097, E225000098, E225000099, E225000100, E230200001, E230200002, E230200003, E230200004, E230200005, E230200006, E230200007, E230200008, E230200009, E230200010, E230200011, E230200012, E230200013, E230200014, E230200015, E230200016, E230200017, E230200018, E230200019, E230200020, E230200021, E230200022, E230200023, E230200024, E230200025, E230200027, E230200028, E230200029, E230200030, E230200031, E230200032, E230200033, E230200034, E230200035, E230200036, E230200037, E230200038, E230200039, E230200040, E230200041, E230200042, E230200043, E230200044, E230200045, E230200046, E230200048, E230200049, E230200050, E230200051, E230200052, E230200053, E230200054, E230200056, E230200057, E230200058, E230200059, E230200060, E230200061, E230200062, E230200064, E230200065, E230200066, E230200067, E230200068, E230200069, E230200070, E230200071, E230200072, E230200073, E230200074, E230200075, E230200076, E230200077, E230200078, E230200079, E230200080, E230200081, E230200082, E230200083, E230200085, E230200086, E230200087, E230200088, E230200089, E230200090, E230200091, E230200092, E230200095, E230200096, E230500006, E230500007, E230500008, E230500009, E230500010, E230500011, E230500031, E230500032, E230500033, E230500034, E230500035, E230500036, E230500037, E230500038, E230500039, E230500040, E230500041, E230500042, E230500043, E230500044, E230500045, E230500046, E230500047, E230500048, E230500049, E230500050, E230500051, E230500052, E230500053, E230500054, E230500055, E230500056, E230500057, E230500058, E230500059, E230500060, E230500061, E230500062, E230500063, E230500064, E230500065, E230500066, E230500092, E230500093, E230500094, E230500103, E230500104, E230500105, E230500106, E230500107, E230500108, E230500109, E230500110, E230500111, E230500112, E230900079, E230900080

Where was it sold?

US: AL, NJ, MA, MI, NY, NC, CO, TX, FL, KY, UT, CA, AZ, KS, IL, TN. OUS: El Salvador, Sweden, Canary Islands

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

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