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U.S. Department of Health and Human Services

Class 2 Device Recall Puritan Bennett Cuff Pressure Manager

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 Class 2 Device Recall Puritan Bennett Cuff Pressure Managersee related information
Date Initiated by FirmAugust 22, 2023
Date PostedSeptember 29, 2023
Recall Status1 Open3, Classified
Recall NumberZ-2651-2023
Recall Event ID 92941
510(K)NumberK202874 
Product Classification Cuff, tracheal tube, inflatable - Product Code BSK
ProductPuritan Bennett Cuff Pressure Manager, REF: 180-03
Code Information 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
Recalling Firm/
Manufacturer		 Covidien
6135 Gunbarrel Ave
Boulder CO 80301-3214
For Additional Information Contact
800-962-9888
Manufacturer 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.
FDA Determined
Cause 2		Component design/selection
ActionOn 8/22/23 Medtronic mailed recall notices to risk managers and directors of respiratory care informing them of the following: 1) Discontinue use, quarantine, and return affected devices to the firm. 2) Complete and return the customer confirmation form via email to it to rs.gmbfcamitg@medtronic.com. 3) Forward the notice to all those who need to be aware within your organization or to any organization where the potentially affected product with the specified serial numbers has been transferred or distributed. If you have any questions regarding this communication, contact customer service at 800-962-9888, Option 2. Quality problems can be reported to Quality Assurance at 800-255-6774 option 4.
Quantity in Commerce408
DistributionUS: AL, NJ, MA, MI, NY, NC, CO, TX, FL, KY, UT, CA, AZ, KS, IL, TN. OUS: El Salvador, Sweden, Canary Islands
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database510(K)s with Product Code = BSK
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