Severity
Critical
CriticalClass ICompleted
FDA Drug recall · Reported May 25, 2022
MILK OF MAGNESIA USP, (Magnesium Hydroxide), 2400 mg/30 mL, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Distributed by Major Pharmaceuticals, Livonia, MI 48152, NDC 0904-6846-73.
Microbial Contamination of Non-Sterile Products
Plastikon Healthcare LLC recalled MILK OF MAGNESIA USP, (Magnesium Hydroxide), 2400 mg/30 mL, 30 mL cup, packaged in 10 cup… - a critical-severity action.
MILK OF MAGNESIA USP, (Magnesium Hydroxide), 2400 mg/30 mL, 30 mL cup, packaged in 10 cup… was recalled by Plastikon Healthcare LLC in May 25, 2022. Reason: Microbial Contamination of Non-Sterile Products. Check the official notice for the remedy. Verify recall #D-0867-2022 with the FDA Drug before acting.
The recall
Plastikon Healthcare LLC issued this critical-severity FDA Drug recall-Microbial Contamination of Non-Sterile Products.
- Critical
- severity level
- 14K units
- affected scope
- Class I
- classification
- May 25, 2022
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0867-2022 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0867-2022) was formally reported on May 25, 2022, with the manufacturer initiating the action on March 24, 2022. It is classified under Critical severity (Class I), with a current status of Completed. Plastikon Healthcare LLC is listed as the recalling firm, operating out of Lawrence, KS. Federal records list the affected scope as 14,100 Unit Dose cups.
The documented reason for this recall is: Microbial Contamination of Non-Sterile Products Distribution data in the federal record shows the product reached: Distributed in Indiana for further distribution in the USA.. 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, 5 from FDA Drug - 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.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications 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 high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
14,100 Unit Dose cups
Related Recalls
6
5 from same agency
Product description
MILK OF MAGNESIA USP, (Magnesium Hydroxide), 2400 mg/30 mL, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Distributed by Major Pharmaceuticals, Livonia, MI 48152, NDC 0904-6846-73.
Reason for recall
Microbial Contamination of Non-Sterile Products
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Completed |
| Recall number | D-0867-2022 |
| Date reported | May 25, 2022 |
| Date initiated | March 24, 2022 |
| Recalling firm | Plastikon Healthcare LLC |
| Firm location | Lawrence, KS |
| Affected scope | 14,100 Unit Dose cups |
| Distribution | Distributed in Indiana for further distribution in the USA. |
Profile values are sourced directly from the official FDA Drug 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 (D-0867-2022) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Drug 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? ▼
MILK OF MAGNESIA USP, (Magnesium Hydroxide), 2400 mg/30 mL, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Distributed by Major Pharmaceuticals, Livonia, MI 48152, NDC 0904-6846-73.. Recalled by Plastikon Healthcare LLC. Units affected: 14,100 Unit Dose cups.
Why was this product recalled? ▼
Microbial Contamination of Non-Sterile Products
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 25, 2022. Severity: Critical. Recall number: D-0867-2022.
Where was the recalled product distributed? ▼
Distribution: Distributed in Indiana for further distribution in the USA..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0867-2022) against your product. Visit the official FDA Drug 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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Compare this recall with PRED MILD, prednisolone acetate ophthalmic suspension, USP,… →
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 Drug, reported May 25, 2022. 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.