Severity
Low
LowClass IIITerminated
FDA Devices recall · Reported November 7, 2018
Palcam Agar Base, Acumedia, PN 7669, Product Usage - Dehydrated culture media used with supplements as a selective and differential medium for the detection and isolation of Listeria monocytogenes from foods and environmental samples in a laboratory setting. Not intended for use in the diagnosis of disease or other conditions in humans.
Expiration date on the label is incorrect. Correct expiration date was November 30, 2020 and label on distributed product listed the expiration date as November 30, 2021.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Acumedia Manufacturers, Inc. recalled Palcam Agar Base, Acumedia, PN 7669, Product Usage - Dehydrated culture media used with s… - a low-severity action.
Palcam Agar Base, Acumedia, PN 7669, Product Usage - Dehydrated culture media used with s… was recalled by Acumedia Manufacturers, Inc. in November 7, 2018. Reason: Expiration date on the label is incorrect. Correct expiration date was November 30, 2020 and label on distrib…. Check the official notice for the remedy. Verify recall #Z-0283-2019 with the FDA Devices before acting.
The recall
Acumedia Manufacturers, Inc. issued this low-severity FDA Devices recall-Expiration date on the label is incorrect. Correct expiration date was November 30, 2020 and label on distrib….
- Low
- severity level
- Class III
- classification
- November 7, 2018
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0283-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0283-2019) was formally reported on November 7, 2018, with the manufacturer initiating the action on August 2, 2018. It is classified under Low severity (Class III), with a current status of Terminated. Acumedia Manufacturers, Inc. is listed as the recalling firm, operating out of Lansing, MI. Federal records list the affected scope as 22 bottles.
The documented reason for this recall is: Expiration date on the label is incorrect. Correct expiration date was November 30, 2020 and label on distributed product listed the expiration date as November 30, 2021. Distribution data in the federal record shows the product reached: Worldwide distribution and US nationwide in the states of CA, GA, MN, OR, RI, TX, and WY. Countries of Canada, Mexico, Scotland, and Uruguay.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,422 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
22 bottles
Related Recalls
6
0 from same agency
Product description
Palcam Agar Base, Acumedia, PN 7669, Product Usage - Dehydrated culture media used with supplements as a selective and differential medium for the detection and isolation of Listeria monocytogenes from foods and environmental samples in a laboratory setting. Not intended for use in the diagnosis of disease or other conditions in humans.
Reason for recall
Expiration date on the label is incorrect. Correct expiration date was November 30, 2020 and label on distributed product listed the expiration date as November 30, 2021.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | Z-0283-2019 |
| Date reported | November 7, 2018 |
| Date initiated | August 2, 2018 |
| Recalling firm | Acumedia Manufacturers, Inc. |
| Firm location | Lansing, MI |
| Affected scope | 22 bottles |
| Distribution | Worldwide distribution and US nationwide in the states of CA, GA, MN, OR, RI, TX, and WY. Countries of Canada, Mexico, Scotland, and Uruguay. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-0283-2019) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Palcam Agar Base, Acumedia, PN 7669, Product Usage - Dehydrated culture media used with supplements as a selective and differential medium for the detection and isolation of Listeria monocytogenes from foods and environmental samples in a laboratory setting. Not intended for use in the diagnosis of disease or other conditions in humans.. Recalled by Acumedia Manufacturers, Inc.. Units affected: 22 bottles.
Why was this product recalled? ▼
Expiration date on the label is incorrect. Correct expiration date was November 30, 2020 and label on distributed product listed the expiration date as November 30, 2021.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 7, 2018. Severity: Low. Recall number: Z-0283-2019.
Where was the recalled product distributed? ▼
Distribution: Worldwide distribution and US nationwide in the states of CA, GA, MN, OR, RI, TX, and WY. Countries of Canada, Mexico, Scotland, and Uruguay..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0283-2019) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported November 7, 2018. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.