Severity
Low
FDA Drug recall · Reported April 18, 2018
Labeling: Incorrect or Missing Lot and/or Exp Date
Lake Erie Medical & Surgical Supply Inc recalled Tramadol Hydrochloride 50 mg tablets, 120-count, Rx Only; Distributed by Quality Care Pro… - a low-severity action.
Tramadol Hydrochloride 50 mg tablets, 120-count, Rx Only; Distributed by Quality Care Pro… was recalled by Lake Erie Medical & Surgical Supply Inc in April 18, 2018. Reason: Labeling: Incorrect or Missing Lot and/or Exp Date. Check the official notice for the remedy. Verify recall #D-0626-2018 with the FDA Drug before acting.
The recall
Lake Erie Medical & Surgical Supply Inc issued this low-severity FDA Drug recall-Labeling: Incorrect or Missing Lot and/or Exp Date.
Sourced from official FDA Drug enforcement records. Verify recall #D-0626-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-0626-2018) was formally reported on April 18, 2018, with the manufacturer initiating the action on March 19, 2018. It is classified under Low severity (Class III), with a current status of Terminated. Lake Erie Medical & Surgical Supply Inc is listed as the recalling firm, operating out of Holland, OH. Federal records list the affected scope as 16 paper cartons.
The documented reason for this recall is: Labeling: Incorrect or Missing Lot and/or Exp Date Distribution data in the federal record shows the product reached: FL, VA. 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, 6 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.
Where this recall sits in its category - 14,436 drugs & medications recalls on record
Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. 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.
Severity
Low
Affected scope
16 paper cartons
Related Recalls
6
6 from same agency
Tramadol Hydrochloride 50 mg tablets, 120-count, Rx Only; Distributed by Quality Care Products, Temperance, MI 48182 Mfr. CSPC Ouyl Pharm Co., Ltd. Shijazhuang, Hebei, China; NDC 55700-0412-01
Labeling: Incorrect or Missing Lot and/or Exp Date
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-0626-2018 |
| Date reported | April 18, 2018 |
| Date initiated | March 19, 2018 |
| Recalling firm | Lake Erie Medical & Surgical Supply Inc |
| Firm location | Holland, OH |
| Affected scope | 16 paper cartons |
| Distribution | FL, VA |
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.
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.
Two federal-filing-derived peer sets for this notice, both outside the same recalling firm and filing state so the neighborhoods are not firm or geographic containment.
Same archive severity grade (Low), closest by report date among other firms and states.
Same product category, closest by report date among other firms and states (deduped against the severity set).
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 April 18, 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 August 2026.