Severity
Moderate
ModerateClass IICompleted
FDA Devices recall · Reported December 21, 2022
CarePoint 60 mL Syringe Without Needle, REF: 04-7560
Syringe without needle may have a green substance on the plunger. Substance found to be nontoxic but its effect on drug potency or interaction is unknown.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Allison Medical, Inc. recalled CarePoint 60 mL Syringe Without Needle, REF: 04-7560 - a moderate-severity action.
CarePoint 60 mL Syringe Without Needle, REF: 04-7560 was recalled by Allison Medical, Inc. in December 21, 2022. Reason: Syringe without needle may have a green substance on the plunger. Substance found to be nontoxic but its effe…. Check the official notice for the remedy. Verify recall #Z-0478-2023 with the FDA Devices before acting.
The recall
Allison Medical, Inc. issued this moderate-severity FDA Devices recall-Syringe without needle may have a green substance on the plunger. Substance found to be nontoxic but its effe….
- Moderate
- severity level
- Class II
- classification
- December 21, 2022
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0478-2023 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0478-2023) was formally reported on December 21, 2022, with the manufacturer initiating the action on September 3, 2020. It is classified under Moderate severity (Class II), with a current status of Completed. Allison Medical, Inc. is listed as the recalling firm, operating out of Littleton, CO. Federal records list the affected scope as 2,004 Boxes.
The documented reason for this recall is: Syringe without needle may have a green substance on the plunger. Substance found to be nontoxic but its effect on drug potency or interaction is unknown. Distribution data in the federal record shows the product reached: US: IA, LA, MS, FL, PR; OUS: BARBADOS. 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, 3 from FDA Devices - 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 - 40,322 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 moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
2,004 Boxes
Related Recalls
6
3 from same agency
Product description
CarePoint 60 mL Syringe Without Needle, REF: 04-7560
Reason for recall
Syringe without needle may have a green substance on the plunger. Substance found to be nontoxic but its effect on drug potency or interaction is unknown.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Completed |
| Recall number | Z-0478-2023 |
| Date reported | December 21, 2022 |
| Date initiated | September 3, 2020 |
| Recalling firm | Allison Medical, Inc. |
| Firm location | Littleton, CO |
| Affected scope | 2,004 Boxes |
| Distribution | US: IA, LA, MS, FL, PR; OUS: BARBADOS |
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-0478-2023) 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? ▼
CarePoint 60 mL Syringe Without Needle, REF: 04-7560. Recalled by Allison Medical, Inc.. Units affected: 2,004 Boxes.
Why was this product recalled? ▼
Syringe without needle may have a green substance on the plunger. Substance found to be nontoxic but its effect on drug potency or interaction is unknown.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 21, 2022. Severity: Moderate. Recall number: Z-0478-2023.
Where was the recalled product distributed? ▼
Distribution: US: IA, LA, MS, FL, PR; OUS: BARBADOS.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0478-2023) 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.
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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 December 21, 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.