Reported Aug 26, 2026 · Ongoing · Updated Sep 7, 2026
American Contract Systems medical procedure kits and trays labeled as
American Contract Systems Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: American Contract Systems Inc · 85 Shaffer Park Dr · Tiffin, OH · 44883-9290
Is this the product you have?
American Contract Systems medical procedure kits and trays labeled as
9 of 9 products
| # | Product as published |
|---|---|
| 1 | CRANI PACK - 208400, Model Item Number UDCP57AI |
| 2 | SPINE PACK, Model Item Number HSLM53AC |
| 3 | CRANIAL PACK - 205992, Model Item Number MHCP75AH |
| 4 | IMRI CRANI PACK - 213871, Model Item Number ANCI17AO |
| 5 | CRANI PACK - 205942, Model Item Number ANCP30AP |
| 6 | A-P PACK - 205936, Model Item Number ANAP22AP |
| 7 | POSTERIOR PACK - 205960, Model Item Number ANPP15AR |
| 8 | ANTERIOR CERVICAL PACK - 205935, Model Item Number ANAN51AI |
| 9 | LAMINECTOMY PACK - 205957, Model Item Number ANLM40AG. |
- Lot codes and dates
62 of 62 products
Products covered by this recall Model / number Barcodes Product as published UDCP57AI191072216250Model/ , UDI/DI 191072216250, Lot Number 42-8388111 UDCP57AI191072216250Model/ , UDI/DI 191072216250, Lot Number 42-8474311 UDCP57AI191072216250Model/ , UDI/DI 191072216250, Lot Number 42-8521711 UDCP57AI191072216250Model/ , UDI/DI 191072216250, Lot Number 42-8547611 UDCP57AI191072216250Model/ , UDI/DI 191072216250, Lot Number 42-8672411 UDCP57AI191072216250Model/ , UDI/DI 191072216250, Lot Number 42-8775211 UDCP57AI191072216250Model/ , UDI/DI 191072216250, Lot Number 42-8810511 HSLM53AC191072238207Model/ , UDI/DI 191072238207, Lot Number 42-8447111 HSLM53AC191072238207Model/ , UDI/DI 191072238207, Lot Number 42-8548311 HSLM53AC191072238207Model/ , UDI/DI 191072238207, Lot Number 42-8630311 HSLM53AC191072238207Model/ , UDI/DI 191072238207, Lot Number 42-8785011 HSLM53AC191072238207Model/ , UDI/DI 191072238207, Lot Number 42-8742911 MHCP75AH191072211934Model/ , UDI/DI 191072211934, Lot Number 42-8455911 MHCP75AH191072211934Model/ , UDI/DI 191072211934, Lot Number 42-8498111 MHCP75AH191072211934Model/ , UDI/DI 191072211934, Lot Number 42-8538111 MHCP75AH191072211934Model/ , UDI/DI 191072211934, Lot Number 42-8601211 MHCP75AH191072211934Model/ , UDI/DI 191072211934, Lot Number 42-8764511 MHCP75AH191072211934Model/ , UDI/DI 191072211934, Lot Number 42-8823811 ANCI17AO191072232052Model/ , UDI/DI 191072232052, Lot Number 42-8384311 ANCI17AO191072232052Model/ , UDI/DI 191072232052, Lot Number 42-8525011 - Amount recalled
- 4789 kits
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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