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Urgent site urgencyFDA Class I

Haylard CONTINUOUS NERVE BLOCK TRAY

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

Agency
FDA Device
Recall date
Aug 10, 2026
Status
Ongoing
Company
AVID Medical, Inc.

1. What product was recalled?

Haylard CONTINUOUS NERVE BLOCK TRAY

Haylard CONTINUOUS NERVE BLOCK TRAY; Model/Item Number (Kit): BMCN001-05;

Quantity: 80 kits

Code or lot text: Model/Item Number (Kit): BMCN001-05; UDI-DI: 10809160455128; Kit Lots: 1703122, 1707656, 1708053; Recalled Sodium Chloride Ampule Lot: AB5002;

LOT
1707656
LOT
1708053
LOT
Kit Lots: 1703122
LOT
Model/Item Number (Kit): BMCN001-05
LOT
Recalled Sodium Chloride Ampule Lot: AB5002
LOT
UDI-DI: 10809160455128
RECALL-NUMBER
Z-3152-2026

2. Is my exact product affected?

Compare every printed identifier. A matching value can indicate that your product is included.

3. What is the hazard?

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

4. What should I do now?

Follow the FDA recall notice and contact the recalling company for current instructions.

5. Where was it sold or distributed?

Illinois, North Carolina, Virginia, Wyoming

View source evidence for state distribution
  • Illinois: Domestic: IL, NC, VA, WY;
  • North Carolina: Domestic: IL, NC, VA, WY;
  • Virginia: Domestic: IL, NC, VA, WY;
  • Wyoming: Domestic: IL, NC, VA, WY;

6. Were injuries or illnesses reported?

No separate injury or illness statement was present in the normalized record. Check the official source for the latest report.

7. What remedy is available?

Follow the FDA recall notice and contact the recalling company for current instructions.

8. Is the recall active or closed?

The source status is Ongoing. The Recall Guy's urgency label is urgent, which is a separate deterministic site label.

9. When was the information checked?

Last checked .

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10. Where is the official source?

Open the official FDA Device source

The Recall Guy normalizes public source data for easier checking. Source agencies remain authoritative. Confirm identifiers and instructions at the official source.