Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported February 19, 2020
Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth.
Teleflex Medical INC recalled Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System - a moderate-severity action.
Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System was recalled by Teleflex Medical INC in February 19, 2020. Reason: The products are being recalled due to reports of breakage broke at the point of a welded joint either prior …. Check the official notice for the remedy. Verify recall #Z-1116-2020 with the FDA Devices before acting.
The recall
Teleflex Medical INC issued this moderate-severity FDA Devices recall-The products are being recalled due to reports of breakage broke at the point of a welded joint either prior ….
- Moderate
- severity level
- Class II
- classification
- February 19, 2020
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1116-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1116-2020) was formally reported on February 19, 2020, with the manufacturer initiating the action on January 9, 2020. It is classified under Moderate severity (Class II), with a current status of Terminated. Teleflex Medical INC is listed as the recalling firm, operating out of Morrisville, NC. Federal records list the affected scope as 338,928 (199,018 US and 139,910 OUS) for all products.
The documented reason for this recall is: The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth. Distribution data in the federal record shows the product reached: Distributed nationwide in the US and to Puerto Rico; OUS to more than 20 countries; To the following government VA medical Centers: VAMC - KANSAS CITY MO 4801 E Linwood Blvd Kansas City MO 64128-2218. 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, 3 from FDA Devices - 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
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
338,928 (199,018 US and 139,910 OUS) for all products
Related Recalls
6
3 from same agency
Product description
Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
Reason for recall
The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1116-2020 |
| Date reported | February 19, 2020 |
| Date initiated | January 9, 2020 |
| Recalling firm | Teleflex Medical INC |
| Firm location | Morrisville, NC |
| Affected scope | 338,928 (199,018 US and 139,910 OUS) for all products |
| Distribution | Distributed nationwide in the US and to Puerto Rico; OUS to more than 20 countries; To the following government VA medical Centers: VAMC - KANSAS CITY MO 4801 E Linwood Blvd Kansas City MO 64128-2218 |
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-1116-2020) 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? ▼
Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System. Recalled by Teleflex Medical INC. Units affected: 338,928 (199,018 US and 139,910 OUS) for all products.
Why was this product recalled? ▼
The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 19, 2020. Severity: Moderate. Recall number: Z-1116-2020.
Where was the recalled product distributed? ▼
Distribution: Distributed nationwide in the US and to Puerto Rico; OUS to more than 20 countries; To the following government VA medical Centers: VAMC - KANSAS CITY MO 4801 E Linwood Blvd Kansas City MO 64128-2218.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1116-2020) 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.
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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 February 19, 2020. 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.