Summary
The FDA issued a Class II for Puritan Bennett Cuff Pressure Manager, REF: 180-03 by Covidien. Reason: Inadequate internal fixation of the power inlet port to the cuff pressure manager device causes the external power inlet to became dislodged within th.
Details
Source
Device Recall
External ID
Z-2651-2023
Action Date
2023-10-11
Status
Ongoing
Category
device
Product Description
Puritan Bennett Cuff Pressure Manager, REF: 180-03
Lot/Code Info: 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
Quantity Affected: 408
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.
Distribution
US: AL, NJ, MA, MI, NY, NC, CO, TX, FL, KY, UT, CA, AZ, KS, IL, TN. OUS: El Salvador, Sweden, Canary Islands
Type: Voluntary: Firm initiated
Recall Initiated: 2023-08-22
Company
Boulder, CO
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 142 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Covidien has 33 FDA actions in our database, including 17 recalls and 16 clearances.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Covidien) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Covidien have FDA actions?
Covidien has 33 FDA actions in our database, including 17 recalls and 16 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-2651-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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