Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported October 31, 2018
Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm, REF Catalog No. NBF13-01130230, UPN BF40180 (Pouch level) - BF40181(Case box level) BF40182 (Carton box level) - BF40183(Over shipper level), STERILE
Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Micro-Tech (Nanjing) Co., Ltd. recalled Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm, REF Catalog No. NBF13-01130230, UPN BF… - a moderate-severity action.
Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm, REF Catalog No. NBF13-01130230, UPN BF… was recalled by Micro-Tech (Nanjing) Co., Ltd. in October 31, 2018. Reason: Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units. Check the official notice for the remedy. Verify recall #Z-0237-2019 with the FDA Devices before acting.
The recall
Micro-Tech (Nanjing) Co., Ltd. issued this moderate-severity FDA Devices recall-Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units.
- Moderate
- severity level
- Class II
- classification
- October 31, 2018
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0237-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0237-2019) was formally reported on October 31, 2018, with the manufacturer initiating the action on September 20, 2018. It is classified under Moderate severity (Class II), with a current status of Terminated. Micro-Tech (Nanjing) Co., Ltd. is listed as the recalling firm, operating out of Nanjing, N/A. Federal records list the affected scope as 1360 pcs.
The documented reason for this recall is: Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units Distribution data in the federal record shows the product reached: US Nationwide Distribution in the states of AL, CA, IN, FL, GA, MO, MT, NV, OK, OR, PA TX & Washington D.C.. 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 - 40,422 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
1360 pcs
Related Recalls
6
0 from same agency
Product description
Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm, REF Catalog No. NBF13-01130230, UPN BF40180 (Pouch level) - BF40181(Case box level) BF40182 (Carton box level) - BF40183(Over shipper level), STERILE
Reason for recall
Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0237-2019 |
| Date reported | October 31, 2018 |
| Date initiated | September 20, 2018 |
| Recalling firm | Micro-Tech (Nanjing) Co., Ltd. |
| Firm location | Nanjing, N/A |
| Affected scope | 1360 pcs |
| Distribution | US Nationwide Distribution in the states of AL, CA, IN, FL, GA, MO, MT, NV, OK, OR, PA TX & Washington D.C. |
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-0237-2019) 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? ▼
Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm, REF Catalog No. NBF13-01130230, UPN BF40180 (Pouch level) - BF40181(Case box level) BF40182 (Carton box level) - BF40183(Over shipper level), STERILE. Recalled by Micro-Tech (Nanjing) Co., Ltd.. Units affected: 1360 pcs.
Why was this product recalled? ▼
Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 31, 2018. Severity: Moderate. Recall number: Z-0237-2019.
Where was the recalled product distributed? ▼
Distribution: US Nationwide Distribution in the states of AL, CA, IN, FL, GA, MO, MT, NV, OK, OR, PA TX & Washington D.C..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0237-2019) 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.
Nearby Recalls in This Category
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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 October 31, 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 July 2026.