Device recalls

Vaporizer Sevoflurane Maquet Filling, Product code/REF number (6682282), Component of: Flow-i C20, Flow-i C30,Flow-i C40, Flow-c, Flow-e.

Getinge Usa Sales Inc · Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health care providers through inhalation and/or…

Open, ClassifiedUnder Investigation by firmZ-1877-2024
Open FDA's page for this record
Cfres ID
207330
Product res number
Z-1877-2024
Event date initiated
2024-05-01
Event date posted
2024-05-31
Recall status
Open, Classified
Res event number
94502
Product code
BSZ
Product description
Vaporizer Sevoflurane Maquet Filling, Product code/REF number (6682282), Component of: Flow-i C20, Flow-i C30,Flow-i C40, Flow-c, Flow-e.
Code info
Part Number 6682282; UDI/DI: 07325710000212: Serial Numbers: 17003 - 23454.
Firm FEI number
3013876692
Recalling firm
Getinge Usa Sales Inc
Address 1
1 Geoffrey Way
City
Wayne
State
NJ
Postal code
07470-2035
Additional info contact
Stephanie Moretti 973-709-7170
Root cause description
Under Investigation by firm
Product quantity
120 units (US)
Reason for recall

Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health care providers through inhalation and/or skin exposure. Potential harms include irritation of respiratory tract, which in worst case may lead to lung edema and/or severe hypocalcemia, blistering, superficial ulceration, and/or hypomagnesemia.

Action

On May 1, 2024 URGENT MEDICAL DEVICE REMOVAL letters were sent to customers. Actions to be taken by customer: Until further notice, do NOT use the Vaproizer with Sevoflurane provided by Poramal and Baxter Sevoflurane. Do NOT use the Vaporizer if it was ever used with Sevoflurane Piramal and/or Baxter Sevoflurane, even if it currently is used with AbbVie Ultane. Our records indicate that you have received the Vaporizer Sevoflurane, Maquet Filling having one or more of the serial numbers that are affected by this recall. 1. Please examine your inventory immediately to determine if you have any of the Vaporizer Sevoflurane, Maquet Filling with the product codes/serial numbers listed in this notice. The Product Code/REF Number and serial number (SN) are found on the label located underneath each vaporizer. Should you have any affected product, please remove from areas of use. 2. If you have ONLY used Vaporizer Product Code/REF Number 6682282, serial number 17003-23454 with AbbVie Ultane, you can continue to use the vaporizer, by certifying that you only use AbbVie Ultane on the Medical Device Recall Response Form. If you are uncertain whether you have previously used the vaporizer with Piramal Sevoflurane and/or Baxter Sevoflurane, discontinue use of the vaporizer. 3. Persuant to the previous recall for the Vaporizer Product Code/REF Number 6886601, you can continue to use this vaporizer so long as it has ONLY been used with Abbvie Ultane. If you are uncertain whether you have previously used the vaporizer with Piramal Sevoflurane and/or Baxter Sevoflurane, discontinue use of the vaporizer. 4. If at any time, the agent in the vaporizer looks cloudy and yellowish, you should immediately stop use of the affected vaporizer. 5. If you have affected product you are entitled to a credit or replacement. Please contact Getinge Customer Service at 888-943-8872 (press option 2) to request a return authorization (RMA) and shipping instructions to return any affected product. Pack

Distribution pattern

Domestic: CA, CO, IN, MO, OR, VA, WA. International: Aruba, Australia, Austria, Belgium, Bolivia, Bosnia-Herzegovina, Brazil, Bulgaria, Chile, China, Costa Rica, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iraq, Israel, Italy, Japan, Jordan, Kenya, Kuwait, Lebanon, Libya, Lithuania, Macau, Macedonia, Malaysia, Mexico, Moldavia, Morocco, Mozambique, Namibia, Netherlands, Nicaragua, Norway, Oman, Pakistan, Paraguay, Peru, Philippines, Poland, Portugal, Romania, Russia, Saudi Arabia, Serbia, Singapore, Slovakia, South Africa, South Korea, Spain, Sweden, Switzerland, Thailand, Tunisia, Turkey, Turkmenistan, Ukraine, United Arab Emirates, United Kingdom, Vietnam Please note that a list of foreign consignees was not provided by the manufacturer and it is not available at this time.

K numbers
K191027
Harmonized identifiers (openFDA)
Device name
Gas-Machine, Anesthesia
Medical specialty description
Anesthesiology
Regulation number
868.5160
Device class
2
K number
K251352, K970163, K830161, K000859, K003663, K011404, K133886, K844008, K101439, K003251, K963481, K855022, K864644, K790456, K171292, K973949, K171311, K151954, K822218, K853435, K041622, K833147, K993410, K781492, K071142, K012446, K030624, K083413, K042607, K060193, K854213, K884802, K925580, K052335, K801100, K905635, K760228, K083098, K981845, K946127 +149 more
Registration number
3003589956, 8043316, 2112667, 1000122786, 9611500, 1066270, 3016618143, 3010157426, 3007238566, 9710602, 3009156722, 2221819, 3014579161, 9617604, 8010042, 3022543477, 3005783425, 1054713, 3007603826, 3009129579, 9610531, 3013188547, 3035111606, 2020813, 3010703925, 2518157, 3021559257, 3000126629, 3005803793, 9611295, 1066427, 1530958, 3049808762
FEI number
3003589956, 1000114111, 2112667, 3003319165, 1000122786, 3016618143, 3010157426, 3007238566, 3009156722, 2221819, 3014579161, 3022543477, 3001104093, 3005783425, 3002558692, 3007603826, 3009129579, 3003513129, 3013188547, 3035111606, 3000957797, 2020813, 3010703925, 2518157, 3021559257, 1000639866, 3000126629, 3005803793, 3002807907, 3007513035, 3002808128, 3002807992, 3049808762
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.