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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 63771

5 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
November 26, 2012
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Perkinelmer

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

5 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 5

NEOGRAM AMINO ACIDS AND ACYLCARNITINES TANDEM MASS SPECTROMETRY KIT Product Number: 3026-0030. This kit is intended for the measurement and evaluation of amino acid, free carnitine, and acylcarnitine concentrations from newborn heel prick blood samples dried on filter paper. (Table 1 of Attachment 2) details the analytes measured by the kit. Quantitative analysis of amino acids, free carnitine and acylcarnitines and their relationship with each other is intended to provide analyte concentration profiles that may aid in the screening of newborns for one or more of several metabolic disorders. This kit is to be used for in vitro diagnostic use only, by trained, qualified laboratory personnel.

Z-0686-2013
Recall number
Z-0686-2013
Initiated
November 26, 2012
Classification
Class II
Status
Terminated
Recalling firm
Perkinelmer
Quantity
180 kits (20 plates/kit)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

Code information

Lot Numbers: 617341, 619236

Distribution pattern

Nationwide Distribution.

device · product 2 of 5

NEOBASE NON-DERIVATIZED MSMS KIT Product Number: 3040-001U. This tandem mass spectrometry (MSMS) reagent kit is intended for the measurement and evaluation of amino acids, succinylacetone, free carnitine, and acylcarnitine concentrations from newborn heel prick blood samples dried on filter paper. Quantitative analysis of these analytes ) and their relationship with each other is intended to provide analyte concentration profiles that may aid in screening newborns for metabolic disorders.

Z-0687-2013
Recall number
Z-0687-2013
Initiated
November 26, 2012
Classification
Class II
Status
Terminated
Recalling firm
Perkinelmer
Quantity
819 kits (10 plates/kit)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

Code information

Lot Numbers: 617253 , 617346, 618494 , 618653, 618764 , 619453

Distribution pattern

Nationwide Distribution.

device · product 3 of 5

NEONATAL TOTAL GALACTOSE KIT Product Numbers: 3029-0010, 3029-001B. This kit is intended for the quantitative determination of total galactose (galactose and galactose-1-phosphate) concentrations in blood specimens dried on filter paper as an aid in screening newborns for galactosemia.

Z-0688-2013
Recall number
Z-0688-2013
Initiated
November 26, 2012
Classification
Class II
Status
Terminated
Recalling firm
Perkinelmer
Quantity
3029-0010 =1562 kits (10 plats/kit) and 3029-001B=13 kits (50plates/kit)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

Code information

Lot Numbers: 618201, 619200, 618263

Distribution pattern

Nationwide Distribution.

device · product 4 of 5

DBS MICROPLATE, TRUNCATED V-BOTTOMED Product Number: 3033-0010

Z-0689-2013
Recall number
Z-0689-2013
Initiated
November 26, 2012
Classification
Class II
Status
Terminated
Recalling firm
Perkinelmer
Quantity
56 kits (100 plates/kit)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

Code information

Lot Numbers: 618609

Distribution pattern

Nationwide Distribution.

device · product 5 of 5

Microplate, truncated V-bottomed lots included in the above listed products Product Number: 1380 5465. DBS Microplate is a general purpose 96 well microplate used in the preparation and examination of specimens from the human body.

Z-0690-2013
Recall number
Z-0690-2013
Initiated
November 26, 2012
Classification
Class II
Status
Terminated
Recalling firm
Perkinelmer
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

Code information

Lot Numbers: 616792 , 617141 , 617980 , 618319, 618664, 618831, 619175

Distribution pattern

Nationwide Distribution.