Z-1474-2021Class II
Gang Cath Lab Set, Model Number M20858R1.for the administration of IV fluids. Stopcocks and manifolds are...
Abbott Medical / initiated 2021-03-31 / Terminated / root cause: manufacturing process
Smiths Medical ASD Inc. began a recall of Gang Cath Lab Set, Model Number M20858R1.for the administration of IV fluids. Stopcocks and manifolds are used to control the direction of IV fluid flow on . FDA classified it as Class II and gives the reason as "Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds, Stopcocks and Tubing and Medex LogiCal Kits may have been manufactured with insufficient or incomplete welds. These are components for various cardiac...". As of , the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.
Recall record
- Recall number
- Z-1474-2021
- Classification
- Class II
- Status
- Terminated
- Initiated
- Posted
- Terminated
- Recalling firm
- Abbott Medical
- Product
- Gang Cath Lab Set, Model Number M20858R1.for the administration of IV fluids. Stopcocks and manifolds are used to control the direction of IV fluid flow.
- Product code
- FPB Filter, Infusion Line
- Reason for recall
- Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds, Stopcocks and Tubing and Medex LogiCal Kits may have been manufactured with insufficient or incomplete welds. These are components for various cardiac kits including pressure monitoring devices and interventional imaging devices.
- Root cause tag
- manufacturing process
- FDA root cause
- Process control
- Action
- The firm initiated the action by email on 03/31/2021. The Recall Notice instructs consignees to identify, and quarantine affected product in their possession. A list of affected product has been included on the Recall Notice for consignees to identify affected product. The consignees have been instructed to complete the response form, and return it to [email protected] within 10 days of receipt. After the completed Recall Response Form has been submitted to [email protected], the consignee will be contacted to arrange return of any affected product in their possession. Distributors have been instructed that if they have distributed potentially affected product to their customers to immediately notify them of the Recall.
- Quantity in commerce
- 400 devices
- Distribution
- Distribution US nationwide including Puerto Rico, Austria, Canada, Chile, Ecuador, Hong Kong, Mexico, Slovenia, Brazil, South Africa, Colombia, and Japan.
- Product codes and lots
- Lot Numbers: 4007165
Enforcement reports
One row per recalled product line| Recall number | Class | Status | Voluntary or mandated | Report date | Classified |
|---|---|---|---|---|---|
| Z-1470-2021 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1471-2021 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1472-2021 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1473-2021 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1474-2021 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1475-2021 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1476-2021 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1477-2021 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1478-2021 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1479-2021 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1480-2021 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-1481-2021 | Class II | Terminated | Voluntary: Firm initiated |
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