PlainRecalls
ModerateClass IITerminated

FDA Drug recall · Reported November 15, 2017

Succinylcholine 20 MG/ML INJ (QUELICIN), 10 ML Vials, Rx only, Distributed by: ACE Surgical Co., Inc., Brockton, MA

Labeling: Incorrect or Missing Lot and/or Exp Date; incorrect expiration date on the labeling of the outer poly bag

Recall #
D-0071-2018
Affected scope
200 vials (25 mislabeled vials)
Initiated
October 24, 2017
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
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Ace Surgical Supply Co., Inc. recalled Succinylcholine 20 MG/ML INJ (QUELICIN), 10 ML Vials, Rx only, Distributed by: ACE Surgic… - a moderate-severity action.

Succinylcholine 20 MG/ML INJ (QUELICIN), 10 ML Vials, Rx only, Distributed by: ACE Surgic… was recalled by Ace Surgical Supply Co., Inc. in November 15, 2017. Reason: Labeling: Incorrect or Missing Lot and/or Exp Date; incorrect expiration date on the labeling of the outer p…. Check the official notice for the remedy. Verify recall #D-0071-2018 with the FDA Drug before acting.

The recall

Ace Surgical Supply Co., Inc. issued this moderate-severity FDA Drug recall-Labeling: Incorrect or Missing Lot and/or Exp Date; incorrect expiration date on the labeling of the outer p….

Moderate
severity level
Class II
classification
November 15, 2017
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-0071-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Drug action (record #D-0071-2018) was formally reported on November 15, 2017, with the manufacturer initiating the action on October 24, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. Ace Surgical Supply Co., Inc. is listed as the recalling firm, operating out of Brockton, MA. Federal records list the affected scope as 200 vials (25 mislabeled vials).

The documented reason for this recall is: Labeling: Incorrect or Missing Lot and/or Exp Date; incorrect expiration date on the labeling of the outer poly bag Distribution data in the federal record shows the product reached: Product was distributed throughout the United States.. 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 - 40,322 medical devices recalls on record

-1,00001,0002,0003,0004,000 20052008201120142017202020232026 1,248
Severity2487872426High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

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.

Severity

Moderate

Affected scope

200 vials (25 mislabeled vials)

Related Recalls

6

0 from same agency

Product description

Succinylcholine 20 MG/ML INJ (QUELICIN), 10 ML Vials, Rx only, Distributed by: ACE Surgical Co., Inc., Brockton, MA

Reason for recall

Labeling: Incorrect or Missing Lot and/or Exp Date; incorrect expiration date on the labeling of the outer poly bag

Recall Profile

Structured summary of the FDA Drug recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number D-0071-2018
Date reported November 15, 2017
Date initiated October 24, 2017
Recalling firm Ace Surgical Supply Co., Inc.
Firm location Brockton, MA
Affected scope 200 vials (25 mislabeled vials)
Distribution Product was distributed throughout the United States.

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-0071-2018) 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.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. 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?
Succinylcholine 20 MG/ML INJ (QUELICIN), 10 ML Vials, Rx only, Distributed by: ACE Surgical Co., Inc., Brockton, MA. Recalled by Ace Surgical Supply Co., Inc.. Units affected: 200 vials (25 mislabeled vials).
Why was this product recalled?
Labeling: Incorrect or Missing Lot and/or Exp Date; incorrect expiration date on the labeling of the outer poly bag
Which agency issued this recall?
This recall was issued by the FDA Drug on November 15, 2017. Severity: Moderate. Recall number: D-0071-2018.
Where was the recalled product distributed?
Distribution: Product was distributed throughout the United States..
How do I check if my product is affected by a recall?
Check the product description and recall number (D-0071-2018) 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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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 November 15, 2017. 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.