Quidel Triage BNP Calibrators Recalled Due to Shipment Compromise
Medline Industries is recalling 26 Quidel Triage BNP Calibrators because the product was compromised during shipment. The recall affects domestic distribution in CA, NY, TX, and VA.
What this means for you
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, but the source text does not report any hospitalizations, injuries, or illnesses. The hazard is limited to product compromise during shipment without confirmed harm, fitting the criteria for a moderate severity score.
Plain-English summary
Medline Industries Inc is recalling 26 units of the Quidel Triage BNP Calibrators. The recall was initiated because the product was compromised during shipment. The affected devices are identified by Model Number ALR98202 and specific lot numbers with expiration dates ranging from December 31, 2019, to March 31, 2021.
The recall covers domestic distribution only to California, New York, Texas, and Virginia. The source text does not specify the exact nature of the compromise or any reported injuries or illnesses associated with the use of these devices.
Consumers and healthcare facilities should stop using the affected Quidel Triage BNP Calibrators and contact Medline Industries Inc for further instructions on return or disposal.
The recalled product
- Product
- The Quidel Triage BNP Calibrators
- Manufacturer
- Medline Industries Inc
- Hazard
- Affected units
- 26
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 (7)
- Model Number: ALR98202 Expiration date: Lot 832243
- exp date 12/31/19 Lot 832570
- exp date 03/31/20 Lot 921292
- exp date 08/31/20 Lot 921565
- exp date 12/31/20 Lot 921836
- exp date 02/28/21 Lot 922069
- exp date 03/31/21
Distribution
Related recalls
Same manufacturer · Medline Industries Inc
See all →- HighMedline Chest Tube Kit Recalled for Non-Sterile Tape Component
FDA (Devices) · 2022-09-14
- ModerateMedline Hand Sanitizer Foam Recalled for Defective Containers
FDA (Drugs) · 2021-12-29
- ModerateBedside PICC CDS Convenience Kit Recalled for Expired Saline Component
FDA (Devices) · 2021-12-22
- HighMedline Venous Access Pack-LF Recalled for Expired Saline Component
FDA (Devices) · 2021-12-22
- HighEVLP Convenience Pack Recalled for Expired Injectable Component
FDA (Devices) · 2021-12-22