MEERA mobile operating table recallZ-0036-2024 · Getinge Usa Sales Inc · initiated Sep 6, 2023
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Getinge Usa Sales Inc or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Under certain conditions, an issue might prevent the device from performing as intended. A specific sequence of commands on the control unit activates the traction drive and triggers an unintended driving (autodrive) of max. 7 sec. may result in the following reasonably foreseeable injury or damage to the health of patients and/or users
FDA root cause category: Software Manufacturing/Software Deployment
What the company is doing
Maquet GMBH / Getinge initiated Urgent Medical Device Correction letter on 9/6/23 via Fed'X. Letter states reason for recall, health risk and action to take: Please examine your inventory immediately to determine if you have any of the Meera Mobile Operating Table with the serial numbers listed in this notice. Maintain awareness on this notice and related actions until your operating table has been updated to ensure effectiveness of the corrective action. Please complete and sign the attached MEDICAL DEVICE CORRECTION- RESPONSE FORM (page 4) to acknowledge that you have received this notification. Return the completed form to Maquet/Getinge by e-mailing a scanned copy to [email protected] or by faxing the form to 800-746-3592 Please forward this information to all current and potential Meera Mobile Operating Table users within your hospital / facility. If you are a distributor who has shipped any affected products to customers, please forward this document to their attention for appropriate action. Getinge has developed a correction to address this issue. A Getinge Service representative will contact you to schedule the correction. This work will be done at no cost to your facility. If you have any questions, please contact your Maquet /Getinge representative Getinge Technical Support at (888) 943-8872 (press option 4, then option 2, then option 1) Monday through Friday, between the hours of 8:00 a.m. and 6:00 p.m. (Eastern Time Zone).
Recall details
- Recall number
- Z-0036-2024
- Status
- Open, Classified
- Initiated by the company
- Sep 6, 2023
- Posted by the FDA
- Oct 4, 2023
- Recalling firm
- Getinge Usa Sales Inc
- Quantity
- 224 units
- Product code
- FQO
- Distribution
- US Nationwide distribution.
Product description
Meera Mobile Operating Table-to support and position the patient immediately before, during and after surgical interventions as well as for examination and treatment. Model Number: 7200.01F2
Code information (models, lots, serial numbers)
Show the full code information (1k characters)
UDI Code: 04046768124363 Serial Numbers: 7 10 9 18 16 14 15 17 13 24 21 22 23 20 25 19 26 32 28 29 30 31 27 42 44 45 46 47 48 49 50 51 54 59 60 52 53 56 57 63 67 74 64 68 72 73 65 69 70 71 66 75 77 78 80 81 82 79 89 83 84 85 86 87 88 90 91 93 92 94 95 96 104 105 99 101 100 102 98 106 107 108 97 103 113 111 112 114 115 119 110 116 118 125 127 128 132 129 130 131 123 124 126 138 134 135 137 139 141 142 143 140 154 146 156 145 147 149 148 150 151 155 161 165 166 164 167 169 171 170 157 162 159 158 163 168 172 174 175 178 179 176 177 152 153 180 181 183 185 182 186 193 196 188 195 189 192 194 190 502 503 504 505 506 507 510 508 509 511 512 513 514 516 520 524 523 521 527 518 519 534 535 536 532 533 541 538 539 537 540 544 545 546 547 548 549 553 550 551 554 555 557 558 556 561 563 564 565 566 569 571 572 567 573 581 579 580 583 585 586 587 584 588 589
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- MEERA mobile operating table 720001F2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
Product lines
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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