Medicrea International recalls Universal Counter Torque (A22020500) due to incompatibility with Pass TULIP [Spinal] System nut drivers. Affected units may cause improper installation.
Incompatible universal counter torque (A22020500) with the nut driver T30 (A22020220)
Medicrea International is recalling its Universal Counter Torque (A22020500) because it is incompatible with the Pass TULIP [Spinal] System's nut driver (A22020220). This could lead to improper installation if used together.
The Universal Counter Torque (A22020500) is designed to be incompatible with the Pass TULIP [Spinal] System's nut driver (A22020220). Using them together could result in improper installation, potentially causing issues with spinal surgery equipment.
Users of the Pass TULIP [Spinal] System who have the Universal Counter Torque (A22020500) model are affected. Medical professionals using this specific combination are most at risk.
Check for the model number A22020500 on the Universal Counter Torque. This product was sold with the Pass TULIP [Spinal] System and has a lot number of 19H0108 and expiration date of 19/08/2029.
Verify if your Universal Counter Torque (A22020500) is compatible with the Pass TULIP [Spinal] System nut driver (A22020220).
The product is incompatible with the Pass TULIP [Spinal] System's nut driver, so it should not be used together. Proper installation requires compatible parts.
The recall does not specify a remedy, so check compatibility with the Pass TULIP [Spinal] System before use.
Look for the model number A22020500 on the Universal Counter Torque, which was sold with the Pass TULIP [Spinal] System and has lot number 19H0108.
We’ve drafted a message you can send Medicrea International to request your refund or repair — edit it as you like.
Subject: Recall Z-1234-2020 — Medicrea International Medicrea International Hello, I own a Medicrea International that is covered by recall Z-1234-2020 from Medicrea International. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
