Gardner Denver Thomas Recalls Medi-Pump Aspirators Due to Performance Issues
Gardner Denver Thomas is recalling 508 Medi-Pump aspirators because the vacuum pump may not perform to specification.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the source text does not report any illnesses, injuries, or hospitalizations, fitting the criteria for a moderate severity score.
Plain-English summary
Gardner Denver Thomas Inc is recalling 508 units of the THOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1243. The recall is being conducted because the vacuum pump may not perform to specification.
The affected units have serial numbers 2122-2629. These medical aspirators were distributed internationally in Mexico, Peru, El Salvador, Chile, Colombia, Vietnam, and Malaysia.
Consumers and healthcare facilities should stop using the affected units and contact the recalling firm for further instructions.
The recalled product
- Product
- THOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1243 Product Usage: medical aspirator
- Manufacturer
- Gardner Denver Thomas Inc
- Category
- Medical Device — Aspirator
- Hazard
- Affected units
- 508
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Serial numbers 2122-2629
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 3 recalled by Gardner Denver Thomas Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 3 products in this recall →Related recalls
Same manufacturer · Gardner Denver Thomas Inc
See all →- ModerateGardner Denver MEDI-PUMP Aspirator Recalled for Performance Defects
FDA (Devices) · 2015-07-29
- ModerateGardner Denver MEDI-PUMP Aspirator Recalled for Performance Defects
FDA (Devices) · 2015-07-29
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