DeviceSignal · Recall classified

American Contract Systems Inc

FDA classified a device recall on 2026-08-20 · Class II · Z-2990-2026

EventRecall classified
Effective2026-08-20
ClassificationClass II

On 2026-08-20 the FDA classified a device recall from American Contract Systems Inc as Class II. Product: American Contract Systems medical procedure kits and trays labeled as: 1) ANTERIOR…. Recall Z-2990-2026. The firm initiated it on 2026-05-19. This reports the classification FDA published on that date.

Reported facts

Recall number
Z-2990-2026
Classification
Class II
Classified on
2026-08-20
Initiated on
2026-05-19
Firm
American Contract Systems Inc
Reason
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.
Product
American Contract Systems medical procedure kits and trays labeled as: 1) ANTERIOR CERVICAL PACK - 205988, Model Item Number MHAC65AH; 2) SPINE PACK - 206013, Model Item Number MHSP99AF.

Every field above is as fda_device_enforcement published it. Nothing on this page is our interpretation.

Provenance

Source
fda_device_enforcement
Source record
Z-2990-2026
Snapshot hash
ab5ada73bf212eb52a548aab0968a0fcee42807c61b0350e60e24bb6e2beed72
Source URL
https://download.open.fda.gov/device/enforcement/device-enforcement-0001-of-0001.json.zip
Observed
2026-09-08T16:22:09.483Z
Transform
fda_device_enforcement_to_recall v1
Event rule
fda_device_recall_classified v1
Event key
25026ed498755a398939b9093d68a783608b92c9f9a02efbd5bb0319ac1bb084
Signal type
device_recall.classified

Source terms that apply

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Data provided by the U.S. Food and Drug Administration (https://open.fda.gov)