Getinge Meera Mobile Operating Table recall
GETINGE MEERA MOBILE OPERATING TABLE: (1) Part 720001B2 (2) Part 720001B0 (3) Part 720001F2 (4) Part 720001F0 (5) Part 710001B2 (6) Part 710001B0 (7)…
Why was Getinge Meera Mobile Operating Table recalled?
User may suffer an electric shock when coming in contact with the exposed electronic components
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
(1) Part 720001B2 S/N 1 to S/N 416 (2) Part 720001B0 S/N 1 to S/N 1416 (3) Part 720001F2 S/N 1 to S/N 91 (4) Part 720001F0 S/N 1 to S/N 220 (5) Part 710001B2 S/N 1 to S/N 8 (6) Part 710001B0 S//N 1 to S/N 11 (7) Part 710001F0 S/N 1 Expanded lots: 720001B2 SN 417 to SN 503 720001B0 SN 1417 to SN 1689 720001F2 SN 92 to SN 119 720001F0 SN 221 to SN 226 and SN 701 to 711 710001B2 SN 9 to SN 14 710001B0 SN 12 to SN 88
- Product
- GETINGE MEERA MOBILE OPERATING TABLE: (1) Part 720001B2 (2) Part 720001B0 (3) Part 720001F2 (4) Part 720001F0 (5) Part 710001B2 (6) Part 710001B0 (7)…
- Recalling firm
- Maquet Cardiovascular Us Sales, Llc
- Quantity
- U.S: 163; Foreign: 1864. Expanded: US:27 Foreign: 455
- Distribution
- Worldwide - US Nationwide Distribution Foreign: ALGERIA ANGOLA ARGENTINA AUSTRALIA AUSTRIA BAHRAIN BANGLADESH BELGIUM BOLIVIA BOTSWANA BOSNIA AND HERZEGOVINA BRAZIL BULGARIA CANADA CHILE CHINA COLOMBIA COSTA RICA CROATIA CZECH REPUBLIC DENMARK ECUADOR EGYPT FINLAND FRANCE GABON GERMANY GREECE HONG KONG HONDURAS HUNGARY ICELAND INDIA IRAN IRELAND ISRAEL ITALY JAPAN JORDAN KUWAIT LATVIA LEBANON LITHUANIA MACEDONIA MALAYSIA MAURITIUS MEXICO MOLDAVA MONTENEGRO MOROCCO MYANMAR NETHERLANDS NAMIBIA NORWAY NEW ZEALAND PAKISTAN PARAGUAY PERU PHILIPPINES POLAND PORTUGAL ROMANIA SAUDI ARABIA SERBIA SINGAPORE SLOVAKIA SLOVENIA SOUTH AFRICA SOUTH KOREA SPAIN SWEDEN SWITZERLAND SYRIA TAIWAN TANZANIA THAILAND TURKEY TURKMENISTAN UKRAINE UNITED ARAB EMIRATES URUGUAY UNITED KINGDOM VIETNAM
- Recall date
- June 12, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)